Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10055 |
| ensemblid | ENSG00000142230.13 |
| hgncid | 30660 |
| symbol | SAE1 |
| name | SUMO1 activating enzyme subunit 1 |
| refseq_nuc | NM_005500.3 |
| refseq_prot | NP_005491.1 |
| ensembl_nuc | ENST00000270225.12 |
| ensembl_prot | ENSP00000270225.6 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 47130835 |
| end | 47210636 |
| strand | + |
| ver | v1.2 |
| region | chr19:47130835-47210636 |
| region5000 | chr19:47125835-47215636 |
| regionname0 | SAE1_chr19_47130835_47210636 |
| regionname5000 | SAE1_chr19_47125835_47215636 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 346 | 361 | 84 | 68 | 152 | 10 | 45 | 117 | SAE1_chr19_47125835_47215636 | SAE1 | MVEKE others(341): Show |
chr19 | 47125835 | 47215636 |
| a0002 | 0/0 | 346 | 13 | 0 | 0 | 13 | 0 | 0 | 12 | SAE1_chr19_47125835_47215636 | SAE1 | MVEKE others(341): Show |
chr19 | 47125835 | 47215636 |
| a0003 | 0/0 | 346 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SAE1_chr19_47125835_47215636 | SAE1 | MVEKE others(341): Show |
chr19 | 47125835 | 47215636 |
| a0004 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | MVEKE others(341): Show |
chr19 | 47125835 | 47215636 |
| a0005 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | MVEKE others(341): Show |
chr19 | 47125835 | 47215636 |
| a0006 | 0/0 | 346 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | MVEKE others(341): Show |
chr19 | 47125835 | 47215636 |
| a0007 | 0/0 | 346 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | MVEKE others(341): Show |
chr19 | 47125835 | 47215636 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1038 | 353 | 83 | 65 | 152 | 9 | 42 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0001c0003 | 0/0 | 1038 | 3 | 0 | 1 | 0 | 0 | 2 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0001c0004 | 0/0 | 1038 | 3 | 0 | 1 | 0 | 1 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0001c0006 | 0/0 | 1038 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0001c0011 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0002c0002 | 0/0 | 1038 | 13 | 0 | 0 | 13 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0003c0005 | 0/0 | 1038 | 2 | 0 | 0 | 2 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0004c0010 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0005c0008 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0006c0007 | 0/0 | 1038 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 | ||
| a0007c0009 | 0/0 | 1038 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ATGGT others(1033): Show |
chr19 | 47125835 | 47215636 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2522 | 335 | 71 | 65 | 146 | 9 | 42 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0001t0002 | 0/0 | 2522 | 7 | 7 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0001t0003 | 0/0 | 2522 | 4 | 4 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0001t0004 | 0/0 | 2522 | 2 | 0 | 0 | 2 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0001t0005 | 0/0 | 2522 | 2 | 0 | 0 | 2 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0001t0007 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0001t0008 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0001t0009 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0003t0001 | 0/0 | 2522 | 3 | 0 | 1 | 0 | 0 | 2 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0004t0001 | 0/0 | 2522 | 3 | 0 | 1 | 0 | 1 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0006t0001 | 0/0 | 2522 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0001c0011t0001 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0002c0002t0001 | 0/0 | 2522 | 13 | 0 | 0 | 13 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0003c0005t0001 | 0/0 | 2522 | 2 | 0 | 0 | 2 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0004c0010t0001 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0005c0008t0006 | 0/0 | 2522 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0006c0007t0001 | 0/0 | 2522 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| a0007c0009t0001 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | ACTCC others(2517): Show |
chr19 | 47125835 | 47215636 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0352 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0001t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0003t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0004t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0006t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0001c0011t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0003c0005t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0003c0005t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0004c0010t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0005c0008t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0006c0007t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| a0007c0009t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0321 | EUR | GBR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0358 | EUR | FIN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0378 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0148 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0371 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0323 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01243 | hp2 | a0001 | c0006 | t0001 | g0210 | AMR | PUR | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0368 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0072 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0073 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0380 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0373 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0231 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03098 | hp1 | a0004 | c0010 | t0001 | g0293 | AFR | MSL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03195 | hp2 | a0005 | c0008 | t0006 | g0104 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0068 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0379 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | MSL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0367 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0325 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0372 | SAS | BEB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG04204 | hp1 | a0006 | c0007 | t0001 | g0244 | SAS | STU | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0365 | SAS | STU | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | CHB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | CHB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18957 | hp1 | a0003 | c0005 | t0001 | g0324 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18981 | hp1 | a0001 | c0001 | t0009 | g0164 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | LWK | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19063 | hp2 | a0007 | c0009 | t0001 | g0241 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19070 | hp2 | a0003 | c0005 | t0001 | g0338 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ASW | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ASW | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | GIH | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02109 | hp1 | a0001 | c0011 | t0001 | g0343 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | USA | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | USA | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | USA | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | LWK | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | LWK | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0125 | REF | REF | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0352 | REF | REF | SAE1_chr19_47125835_47215636 | SAE1 | chr19 | 47125835 | 47215636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47143522 | G | A | 1 | a0006 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.127G>A | p.Gly43Ser | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/9 | 223/2522 | 127/1041 | 43/346 | chr19 | 47143522 | |||
| chr19:47150310 | G | A | 1 | a0005 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.319G>A | p.Asp107Asn | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/9 | 415/2522 | 319/1041 | 107/346 | chr19 | 47150310 | |||
| chr19:47169873 | A | G | 1 | a0004 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.683A>G | p.Lys228Arg | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/9 | 779/2522 | 683/1041 | 228/346 | chr19 | 47169873 | |||
| chr19:47197268 | C | T | 1 | a0007 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.769C>T | p.Pro257Ser | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/9 | 865/2522 | 769/1041 | 257/346 | chr19 | 47197268 | |||
| chr19:47197281 | C | A | 1 | a0003 | 2 | NA18957.hp1 NA19070.hp2 |
missense_variant | MODERATE | c.782C>A | p.Thr261Lys | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/9 | 878/2522 | 782/1041 | 261/346 | chr19 | 47197281 | |||
| chr19:47197374 | T | C | 1 | a0002 | 13 | HG02071.hp1 NA18940.hp2 NA18942.hp2 others(10): Show |
missense_variant | MODERATE | c.875T>C | p.Val292Ala | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/9 | 971/2522 | 875/1041 | 292/346 | chr19 | 47197374 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47143509 | G | C | 1 | a0001c0006 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.114G>C | p.Arg38Arg | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/9 | 210/2522 | 114/1041 | 38/346 | chr19 | 47143509 | |||
| chr19:47169841 | A | G | 1 | a0001c0011 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.651A>G | p.Lys217Lys | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/9 | 747/2522 | 651/1041 | 217/346 | chr19 | 47169841 | |||
| chr19:47197285 | T | C | 1 | a0001c0003 | 3 | HG01070.hp2 HG02683.hp2 HG03239.hp1 |
synonymous_variant | LOW | c.786T>C | p.Tyr262Tyr | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/9 | 882/2522 | 786/1041 | 262/346 | chr19 | 47197285 | |||
| chr19:47197354 | C | T | 1 | a0001c0004 | 3 | HG00099.hp1 HG01106.hp2 HG04184.hp1 |
synonymous_variant | LOW | c.855C>T | p.Asp285Asp | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/9 | 951/2522 | 855/1041 | 285/346 | chr19 | 47197354 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47130843 | C | A | 1 | a0005c0008t0006 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/9 | 88 | chr19 | 47130843 | ||||||
| chr19:47130854 | C | T | 1 | a0001c0001t0009 | 1 | NA18981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-77C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/9 | 77 | chr19 | 47130854 | ||||||
| chr19:47209252 | A | T | 1 | a0001c0001t0008 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 9/9 | 1 | chr19 | 47209252 | ||||||
| chr19:47209427 | C | T | 1 | a0001c0001t0005 | 2 | HG02056.hp2 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*176C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 9/9 | 176 | chr19 | 47209427 | ||||||
| chr19:47209537 | C | A | 1 | a0001c0001t0007 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 9/9 | 286 | chr19 | 47209537 | ||||||
| chr19:47209861 | T | G | 1 | a0001c0001t0004 | 2 | HG02027.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*610T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 9/9 | 610 | chr19 | 47209861 | ||||||
| chr19:47209927 | G | A | 1 | a0001c0001t0008 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*676G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 9/9 | 676 | chr19 | 47209927 | ||||||
| chr19:47210055 | C | T | 1 | a0001c0001t0003 | 4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*804C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 9/9 | 804 | chr19 | 47210055 | ||||||
| chr19:47210349 | G | A | 1 | a0001c0001t0002 | 7 | HG02809.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1098G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 9/9 | 1098 | chr19 | 47210349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47131031 | C | T | 2 | a0001c0001t0001g0379 a0001c0001t0001g0380 |
2 | HG02698.hp2 HG03490.hp1 |
splice_region_variant&intron_variant | LOW | c.98+3C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131031 | |||||||
| chr19:47131056 | T | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(342): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.98+28T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131056 | |||||||
| chr19:47131112 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.98+84G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131112 | |||||||
| chr19:47131224 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.98+196G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131224 | |||||||
| chr19:47131229 | C | G | 1 | a0001c0001t0001g0001 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.98+201C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131229 | |||||||
| chr19:47131231 | G | C | 1 | a0001c0001t0001g0001 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.98+203G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131231 | |||||||
| chr19:47131232 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.98+204T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131232 | |||||||
| chr19:47131255 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.98+227G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131255 | |||||||
| chr19:47131312 | C | T | 1 | a0001c0001t0002g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.98+284C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131312 | |||||||
| chr19:47131425 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.98+397G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131425 | |||||||
| chr19:47131444 | G | C | 2 | a0001c0001t0003g0003 a0001c0001t0003g0004 |
2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.98+416G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131444 | |||||||
| chr19:47131483 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98+455C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131483 | |||||||
| chr19:47131509 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.98+481A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131509 | |||||||
| chr19:47131696 | T | C | 1 | a0001c0001t0001g0005 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.98+668T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131696 | |||||||
| chr19:47131697 | C | CT | 110 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(107): Show |
110 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.98+692dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47131697 | ||||||
| chr19:47131697 | C | CTT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0332 a0001c0001t0001g0333 others(8): Show |
11 | HG02004.hp1 HG02257.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.98+691_98+692dupTT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47131697 | ||||||
| chr19:47131697 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.98+669C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131697 | |||||||
| chr19:47131697 | CT | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(23): Show |
26 | HG01069.hp1 HG01069.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.98+692delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47131697 | ||||||
| chr19:47131697 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0006 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98+681_98+692delTT others(10): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47131697 | ||||||
| chr19:47131727 | GTCTC | G | 45 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0296 others(42): Show |
45 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.98+705_98+708delCT others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47131727 | ||||||
| chr19:47131736 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.98+708T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131736 | |||||||
| chr19:47131759 | G | T | 23 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(20): Show |
23 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.98+731G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131759 | |||||||
| chr19:47131994 | C | G | 19 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(16): Show |
19 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.98+966C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47131994 | |||||||
| chr19:47132027 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(274): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.98+999C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132027 | |||||||
| chr19:47132055 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.98+1027C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132055 | |||||||
| chr19:47132218 | C | A | 1 | a0001c0001t0001g0296 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.98+1190C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132218 | |||||||
| chr19:47132371 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.98+1343C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132371 | |||||||
| chr19:47132393 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.98+1365C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132393 | |||||||
| chr19:47132424 | G | GT | 18 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(15): Show |
18 | HG01433.hp1 HG01934.hp1 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.98+1411dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47132424 | ||||||
| chr19:47132424 | G | T | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0223 |
3 | HG00738.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.98+1396G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132424 | |||||||
| chr19:47132428 | T | G | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.98+1400T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132428 | |||||||
| chr19:47132429 | T | G | 1 | a0001c0001t0001g0375 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.98+1401T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132429 | |||||||
| chr19:47132495 | C | T | 2 | a0001c0001t0001g0379 a0001c0001t0001g0380 |
2 | HG02698.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.98+1467C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132495 | |||||||
| chr19:47132510 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98+1482A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132510 | |||||||
| chr19:47132540 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.98+1512A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132540 | |||||||
| chr19:47132580 | T | C | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0003g0003 others(3): Show |
6 | HG00738.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+1552T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132580 | |||||||
| chr19:47132615 | C | T | 1 | a0001c0001t0001g0374 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.98+1587C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132615 | |||||||
| chr19:47132651 | T | A | 1 | a0001c0001t0001g0345 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.98+1623T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132651 | |||||||
| chr19:47132705 | T | A | 1 | a0001c0001t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.98+1677T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132705 | |||||||
| chr19:47132733 | C | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01496.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.98+1705C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132733 | |||||||
| chr19:47132738 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98+1710A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132738 | |||||||
| chr19:47132757 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98+1729A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132757 | |||||||
| chr19:47132889 | C | CA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(96): Show |
99 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.98+1877dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47132889 | ||||||
| chr19:47132889 | CA | C | 23 | a0001c0001t0001g0085 a0001c0001t0001g0191 a0001c0001t0001g0192 others(20): Show |
23 | HG00733.hp2 HG01070.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.98+1877delA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47132889 | ||||||
| chr19:47132957 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.98+1929G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47132957 | |||||||
| chr19:47133019 | T | C | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02818.hp2 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+1991T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47133019 | |||||||
| chr19:47133055 | T | C | 2 | a0001c0001t0004g0098 a0001c0001t0004g0273 |
2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.98+2027T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47133055 | |||||||
| chr19:47133113 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.98+2085T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47133113 | |||||||
| chr19:47133171 | G | T | 1 | a0002c0002t0001g0034 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.98+2143G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47133171 | |||||||
| chr19:47133213 | G | C | 1 | a0001c0001t0001g0007 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.98+2185G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47133213 | |||||||
| chr19:47133570 | T | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(143): Show |
146 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.98+2542T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47133570 | |||||||
| chr19:47133862 | G | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.98+2834G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47133862 | |||||||
| chr19:47133870 | T | G | 20 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
20 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.98+2842T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47133870 | |||||||
| chr19:47134063 | G | A | 1 | a0001c0001t0002g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.98+3035G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134063 | |||||||
| chr19:47134257 | T | C | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.98+3229T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134257 | |||||||
| chr19:47134351 | G | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(106): Show |
109 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.98+3323G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134351 | |||||||
| chr19:47134407 | G | T | 1 | a0001c0001t0001g0191 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.98+3379G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134407 | |||||||
| chr19:47134408 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.98+3380T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134408 | |||||||
| chr19:47134491 | G | T | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG00621.hp1 NA18949.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+3463G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134491 | |||||||
| chr19:47134503 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.98+3475A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134503 | |||||||
| chr19:47134586 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.98+3558A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134586 | |||||||
| chr19:47134981 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98+3953A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47134981 | |||||||
| chr19:47135019 | T | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.98+3991T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135019 | |||||||
| chr19:47135025 | G | T | 4 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG02886.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+3997G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135025 | |||||||
| chr19:47135035 | A | T | 1 | a0001c0001t0001g0284 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.98+4007A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135035 | |||||||
| chr19:47135111 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0109 |
2 | HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.98+4083G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135111 | |||||||
| chr19:47135282 | A | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(118): Show |
121 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.98+4254A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135282 | |||||||
| chr19:47135299 | A | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0199 a0001c0001t0001g0330 |
3 | HG01934.hp1 HG03195.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.98+4271A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135299 | |||||||
| chr19:47135515 | C | T | 1 | a0002c0002t0001g0033 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.98+4487C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135515 | |||||||
| chr19:47135544 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.98+4516G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135544 | |||||||
| chr19:47135584 | A | C | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98+4556A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135584 | |||||||
| chr19:47135630 | G | A | 7 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(4): Show |
7 | HG00544.hp2 HG00741.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+4602G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135630 | |||||||
| chr19:47135685 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG01123.hp2 HG01978.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.98+4657G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135685 | |||||||
| chr19:47135763 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.98+4735G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135763 | |||||||
| chr19:47135833 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG00741.hp2 HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.98+4805G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135833 | |||||||
| chr19:47135952 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0084 |
2 | HG01257.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.98+4924C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135952 | |||||||
| chr19:47135964 | C | T | 19 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(16): Show |
19 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.98+4936C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47135964 | |||||||
| chr19:47136034 | C | G | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02818.hp2 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+5006C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136034 | |||||||
| chr19:47136170 | G | A | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.98+5142G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136170 | |||||||
| chr19:47136224 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.98+5196C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136224 | |||||||
| chr19:47136346 | C | T | 1 | a0001c0001t0001g0372 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.98+5318C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136346 | |||||||
| chr19:47136394 | C | T | 4 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG02886.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+5366C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136394 | |||||||
| chr19:47136417 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.98+5389C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136417 | |||||||
| chr19:47136494 | CT | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(270): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.98+5484delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47136494 | ||||||
| chr19:47136547 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.98+5519G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136547 | |||||||
| chr19:47136785 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.98+5757C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136785 | |||||||
| chr19:47136822 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.98+5794C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136822 | |||||||
| chr19:47136865 | G | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
21 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.98+5837G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47136865 | |||||||
| chr19:47137155 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98+6127G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137155 | |||||||
| chr19:47137353 | A | G | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99-6141A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137353 | |||||||
| chr19:47137507 | A | T | 19 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(16): Show |
19 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.99-5987A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137507 | |||||||
| chr19:47137703 | T | TTGTGTGT others(7): Show |
1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99-5779_99-5766dup others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47137703 | ||||||
| chr19:47137703 | TTG | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(154): Show |
157 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.99-5767_99-5766del others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47137703 | ||||||
| chr19:47137703 | TTGTGTGT others(1): Show |
T | 8 | a0001c0001t0001g0366 a0001c0001t0001g0367 a0001c0001t0001g0368 others(5): Show |
8 | HG01081.hp1 HG01099.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-5773_99-5766del others(8): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47137703 | ||||||
| chr19:47137703 | TTGTGTGT others(9): Show |
T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.99-5781_99-5766del others(16): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47137703 | ||||||
| chr19:47137724 | TG | T | 7 | a0001c0001t0001g0296 a0001c0001t0001g0303 a0001c0001t0001g0304 others(4): Show |
7 | NA18963.hp2 NA18965.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-5769delG | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137724 | |||||||
| chr19:47137726 | TG | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0186 others(67): Show |
70 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.99-5767delG | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137726 | |||||||
| chr19:47137727 | G | T | 7 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0291 others(4): Show |
7 | HG01928.hp2 HG02135.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-5767G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137727 | |||||||
| chr19:47137728 | T | G | 7 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0291 others(4): Show |
7 | HG01928.hp2 HG02135.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-5766T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137728 | |||||||
| chr19:47137728 | TTG | T | 9 | a0001c0001t0001g0296 a0001c0001t0001g0302 a0001c0001t0001g0303 others(6): Show |
9 | HG04228.hp1 HG04228.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-5764_99-5763del others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47137728 | ||||||
| chr19:47137729 | T | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0186 others(66): Show |
69 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.99-5765T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137729 | |||||||
| chr19:47137730 | G | GT | 11 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0089 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-5748dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47137730 | ||||||
| chr19:47137730 | G | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0186 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.99-5764G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137730 | |||||||
| chr19:47137767 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.99-5727C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47137767 | |||||||
| chr19:47138026 | G | A | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99-5468G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138026 | |||||||
| chr19:47138244 | A | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG02886.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-5250A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138244 | |||||||
| chr19:47138295 | C | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | NA18971.hp1 NA18992.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.99-5199C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138295 | |||||||
| chr19:47138500 | CATT | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(13): Show |
16 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.99-4987_99-4985del others(3): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47138500 | ||||||
| chr19:47138519 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99-4975A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138519 | |||||||
| chr19:47138523 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99-4971G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138523 | |||||||
| chr19:47138660 | C | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0224 a0001c0001t0001g0225 others(42): Show |
45 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.99-4834C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138660 | |||||||
| chr19:47138689 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.99-4805A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138689 | |||||||
| chr19:47138756 | G | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-4738G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138756 | |||||||
| chr19:47138799 | TAGTG | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02647.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.99-4692_99-4689del others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47138799 | ||||||
| chr19:47138817 | A | G | 1 | a0001c0001t0001g0374 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.99-4677A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47138817 | |||||||
| chr19:47139106 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.99-4388C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47139106 | |||||||
| chr19:47139406 | G | A | 3 | a0001c0001t0001g0366 a0001c0001t0001g0367 a0001c0001t0001g0373 |
3 | HG01099.hp1 HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.99-4088G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47139406 | |||||||
| chr19:47139515 | G | C | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99-3979G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47139515 | |||||||
| chr19:47139523 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(118): Show |
121 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.99-3971G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47139523 | |||||||
| chr19:47139586 | C | CT | 38 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0089 others(35): Show |
38 | HG00621.hp2 HG00733.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.99-3889dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47139586 | ||||||
| chr19:47139586 | C | CTT | 81 | a0001c0001t0001g0092 a0001c0001t0001g0224 a0001c0001t0001g0225 others(78): Show |
81 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.99-3890_99-3889dup others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47139586 | ||||||
| chr19:47139586 | CT | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0036 others(3): Show |
6 | HG01975.hp1 HG02735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-3889delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47139586 | ||||||
| chr19:47139652 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.99-3842G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47139652 | |||||||
| chr19:47139670 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99-3824G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47139670 | |||||||
| chr19:47139707 | G | C | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99-3787G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47139707 | |||||||
| chr19:47139737 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.99-3757C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47139737 | |||||||
| chr19:47139755 | A | AT | 28 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0083 others(25): Show |
28 | HG00621.hp1 HG01109.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.99-3720dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47139755 | ||||||
| chr19:47139936 | C | CT | 11 | a0001c0001t0001g0078 a0001c0001t0001g0167 a0001c0001t0001g0168 others(8): Show |
11 | HG01928.hp1 HG01934.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-3539dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47139936 | ||||||
| chr19:47139936 | CT | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(140): Show |
143 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.99-3539delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47139936 | ||||||
| chr19:47139936 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.99-3549_99-3539del others(11): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47139936 | ||||||
| chr19:47140082 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99-3412C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140082 | |||||||
| chr19:47140115 | T | C | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99-3379T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140115 | |||||||
| chr19:47140153 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.99-3341A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140153 | |||||||
| chr19:47140155 | G | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99-3339G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140155 | |||||||
| chr19:47140176 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.99-3318G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140176 | |||||||
| chr19:47140384 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.99-3110G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140384 | |||||||
| chr19:47140623 | C | CA | 127 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(124): Show |
127 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.99-2856dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47140623 | ||||||
| chr19:47140623 | C | CAA | 17 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0118 others(14): Show |
17 | HG00735.hp1 HG01109.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.99-2857_99-2856dup others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47140623 | ||||||
| chr19:47140636 | A | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG03017.hp1 HG03704.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-2858A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140636 | |||||||
| chr19:47140640 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.99-2854C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140640 | |||||||
| chr19:47140808 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.99-2686C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140808 | |||||||
| chr19:47140906 | C | T | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG00733.hp2 HG02109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-2588C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140906 | |||||||
| chr19:47140907 | G | A | 3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | NA18941.hp1 NA18947.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.99-2587G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140907 | |||||||
| chr19:47140940 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(86): Show |
89 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.99-2554T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140940 | |||||||
| chr19:47140953 | A | G | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-2541A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47140953 | |||||||
| chr19:47141121 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG00738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.99-2373T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141121 | |||||||
| chr19:47141146 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.99-2348C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141146 | |||||||
| chr19:47141158 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.99-2336C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141158 | |||||||
| chr19:47141312 | T | G | 1 | a0001c0001t0001g0124 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.99-2182T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141312 | |||||||
| chr19:47141361 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.99-2133C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141361 | |||||||
| chr19:47141380 | GATCCACC others(1): Show |
G | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.99-2110_99-2103del others(8): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47141380 | ||||||
| chr19:47141395 | G | A | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99-2099G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141395 | |||||||
| chr19:47141501 | G | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99-1993G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141501 | |||||||
| chr19:47141642 | G | T | 1 | a0001c0001t0001g0333 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.99-1852G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141642 | |||||||
| chr19:47141643 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.99-1851A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141643 | |||||||
| chr19:47141645 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.99-1849G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141645 | |||||||
| chr19:47141686 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.99-1808A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47141686 | |||||||
| chr19:47142324 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.99-1170T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47142324 | |||||||
| chr19:47142384 | T | TA | 8 | a0001c0001t0001g0197 a0001c0001t0001g0300 a0001c0001t0001g0347 others(5): Show |
8 | HG02109.hp1 HG02280.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-1093dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47142384 | ||||||
| chr19:47142384 | TA | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(113): Show |
116 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.99-1093delA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47142384 | ||||||
| chr19:47142520 | CCAT | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0027 others(96): Show |
99 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.99-969_99-967delAT others(1): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 47142520 | ||||||
| chr19:47142971 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.99-523C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47142971 | |||||||
| chr19:47142975 | C | A | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | NA18952.hp1 NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.99-519C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47142975 | |||||||
| chr19:47143072 | C | G | 1 | a0001c0001t0002g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99-422C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47143072 | |||||||
| chr19:47143213 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99-281C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47143213 | |||||||
| chr19:47143251 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.99-243G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47143251 | |||||||
| chr19:47143262 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99-232C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47143262 | |||||||
| chr19:47143339 | A | G | 1 | a0001c0001t0001g0299 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.99-155A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47143339 | |||||||
| chr19:47143424 | T | G | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.99-70T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47143424 | |||||||
| chr19:47143478 | A | G | 1 | a0001c0003t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.99-16A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47143478 | |||||||
| chr19:47143480 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.99-14T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 1/8 | chr19 | 47143480 | |||||||
| chr19:47143608 | G | T | 1 | a0001c0001t0001g0364 | 1 | NA18747.hp1 | splice_region_variant&intron_variant | LOW | c.210+3G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47143608 | |||||||
| chr19:47143780 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210+175C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47143780 | |||||||
| chr19:47143955 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.210+350G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47143955 | |||||||
| chr19:47144155 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(87): Show |
90 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.210+550A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47144155 | |||||||
| chr19:47144306 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210+701C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47144306 | |||||||
| chr19:47144346 | A | C | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+741A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47144346 | |||||||
| chr19:47144445 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.210+840A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47144445 | |||||||
| chr19:47144496 | G | A | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG02132.hp2 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+891G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47144496 | |||||||
| chr19:47144631 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.210+1026G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47144631 | |||||||
| chr19:47144642 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(157): Show |
160 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.210+1037C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47144642 | |||||||
| chr19:47144647 | C | G | 5 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
5 | HG02647.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+1042C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47144647 | |||||||
| chr19:47145152 | A | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0289 |
2 | NA18963.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.210+1547A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47145152 | |||||||
| chr19:47145182 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.210+1577A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47145182 | |||||||
| chr19:47145495 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.210+1890T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47145495 | |||||||
| chr19:47145511 | C | CAGGCTCA others(11): Show |
1 | a0001c0001t0001g0333 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.210+1908_210+1925d others(20): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47145511 | ||||||
| chr19:47145525 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.210+1920A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47145525 | |||||||
| chr19:47145558 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.210+1953C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47145558 | |||||||
| chr19:47145572 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(85): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.210+1967A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47145572 | |||||||
| chr19:47145859 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0234 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.210+2254A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47145859 | |||||||
| chr19:47145934 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.210+2329A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47145934 | |||||||
| chr19:47145936 | GT | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(319): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.210+2350delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47145936 | ||||||
| chr19:47146103 | G | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0133 |
2 | NA18983.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.210+2498G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47146103 | |||||||
| chr19:47146489 | T | C | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.210+2884T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47146489 | |||||||
| chr19:47146718 | G | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.210+3113G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47146718 | |||||||
| chr19:47147151 | T | C | 1 | a0002c0002t0001g0046 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.211-3051T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147151 | |||||||
| chr19:47147197 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.211-3005G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147197 | |||||||
| chr19:47147199 | G | GT | 27 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0069 others(24): Show |
27 | HG00621.hp2 HG01358.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.211-2975dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47147199 | ||||||
| chr19:47147199 | GT | G | 167 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.211-2975delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47147199 | ||||||
| chr19:47147199 | GTT | G | 48 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(45): Show |
48 | HG01243.hp2 HG01257.hp1 HG01361.hp2 others(45): Show |
intron_variant | MODIFIER | c.211-2976_211-2975d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47147199 | ||||||
| chr19:47147199 | GTTT | G | 8 | a0001c0001t0001g0031 a0001c0001t0001g0204 a0001c0001t0001g0217 others(5): Show |
8 | HG00733.hp2 HG01069.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-2977_211-2975d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47147199 | ||||||
| chr19:47147200 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.211-3002T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147200 | |||||||
| chr19:47147216 | T | G | 1 | a0004c0010t0001g0293 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211-2986T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147216 | |||||||
| chr19:47147232 | C | T | 43 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(40): Show |
43 | HG01070.hp2 HG01074.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.211-2970C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147232 | |||||||
| chr19:47147305 | CAGGGTAT others(1552): Show |
C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0267 |
2 | HG01515.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.211-2896_211-1338d others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147305 | |||||||
| chr19:47147319 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.211-2883A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147319 | |||||||
| chr19:47147614 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-2588G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147614 | |||||||
| chr19:47147651 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.211-2551C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147651 | |||||||
| chr19:47147742 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.211-2460C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147742 | |||||||
| chr19:47147761 | A | AT | 16 | a0001c0001t0001g0084 a0001c0001t0001g0155 a0001c0001t0001g0185 others(13): Show |
16 | HG00642.hp2 HG02080.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.211-2426dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47147761 | ||||||
| chr19:47147762 | T | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0109 |
2 | HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.211-2440T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147762 | |||||||
| chr19:47147822 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(85): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.211-2380G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147822 | |||||||
| chr19:47147832 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.211-2370C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47147832 | |||||||
| chr19:47148080 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0215 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.211-2122C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47148080 | |||||||
| chr19:47148089 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.211-2113G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47148089 | |||||||
| chr19:47148270 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.211-1932G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47148270 | |||||||
| chr19:47148364 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.211-1838T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47148364 | |||||||
| chr19:47148576 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.211-1626C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47148576 | |||||||
| chr19:47148617 | CT | C | 7 | a0001c0001t0001g0119 a0001c0001t0001g0188 a0001c0001t0001g0251 others(4): Show |
7 | HG02080.hp1 HG02965.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-1570delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47148617 | ||||||
| chr19:47148690 | A | C | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.211-1512A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47148690 | |||||||
| chr19:47148690 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.211-1512A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47148690 | |||||||
| chr19:47148758 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.211-1444G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47148758 | |||||||
| chr19:47149163 | C | CT | 40 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0067 others(37): Show |
40 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.211-1014dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47149163 | ||||||
| chr19:47149163 | CT | C | 30 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
30 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.211-1014delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47149163 | ||||||
| chr19:47149210 | G | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.211-992G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47149210 | |||||||
| chr19:47149238 | G | A | 1 | a0001c0001t0005g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.211-964G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47149238 | |||||||
| chr19:47149264 | C | G | 377 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(374): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.211-938C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47149264 | |||||||
| chr19:47149381 | G | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.211-821G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47149381 | |||||||
| chr19:47149423 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.211-779G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47149423 | |||||||
| chr19:47149456 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0051 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-746C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47149456 | |||||||
| chr19:47149623 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.211-579G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47149623 | |||||||
| chr19:47149626 | TAGA | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.211-568_211-566del others(3): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47149626 | ||||||
| chr19:47149840 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.211-362G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47149840 | |||||||
| chr19:47150010 | G | A | 1 | a0001c0001t0002g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211-192G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47150010 | |||||||
| chr19:47150068 | C | G | 6 | a0002c0002t0001g0039 a0002c0002t0001g0062 a0002c0002t0001g0063 others(3): Show |
6 | NA18942.hp2 NA18945.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-134C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47150068 | |||||||
| chr19:47150070 | G | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.211-132G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | chr19 | 47150070 | |||||||
| chr19:47150074 | C | CA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0036 others(109): Show |
112 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.211-107dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47150074 | ||||||
| chr19:47150074 | CA | C | 12 | a0001c0001t0001g0130 a0001c0001t0001g0135 a0001c0001t0001g0155 others(9): Show |
12 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.211-107delA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 47150074 | ||||||
| chr19:47150453 | A | G | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.384+78A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47150453 | |||||||
| chr19:47150945 | T | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.384+570T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47150945 | |||||||
| chr19:47151143 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384+768T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47151143 | |||||||
| chr19:47151189 | G | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.384+814G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47151189 | |||||||
| chr19:47151202 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.384+827T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47151202 | |||||||
| chr19:47151402 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.384+1027C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47151402 | |||||||
| chr19:47151558 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.384+1183G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47151558 | |||||||
| chr19:47151596 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.384+1221G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47151596 | |||||||
| chr19:47151652 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.385-1246T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47151652 | |||||||
| chr19:47152050 | C | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.385-848C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47152050 | |||||||
| chr19:47152104 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.385-794A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47152104 | |||||||
| chr19:47152311 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.385-587T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47152311 | |||||||
| chr19:47152492 | G | T | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-406G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47152492 | |||||||
| chr19:47152509 | G | A | 1 | a0001c0001t0005g0077 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.385-389G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47152509 | |||||||
| chr19:47152796 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.385-102G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 3/8 | chr19 | 47152796 | |||||||
| chr19:47153062 | G | A | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0344 |
3 | HG02886.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.527+22G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153062 | |||||||
| chr19:47153102 | A | T | 18 | a0001c0001t0001g0237 a0001c0001t0001g0240 a0001c0001t0001g0246 others(15): Show |
18 | HG00597.hp1 HG02083.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.527+62A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153102 | |||||||
| chr19:47153280 | T | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.527+240T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153280 | |||||||
| chr19:47153296 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.527+256C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153296 | |||||||
| chr19:47153321 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.527+281A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153321 | |||||||
| chr19:47153778 | G | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0289 |
2 | NA18963.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.527+738G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153778 | |||||||
| chr19:47153780 | A | ATAT | 5 | a0001c0001t0001g0301 a0001c0001t0001g0317 a0001c0001t0001g0341 others(2): Show |
5 | HG01928.hp2 HG02004.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+757_527+759dup others(3): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47153780 | ||||||
| chr19:47153788 | A | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
21 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.527+748A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153788 | |||||||
| chr19:47153894 | C | G | 1 | a0001c0001t0001g0002 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.527+854C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153894 | |||||||
| chr19:47153952 | T | C | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.527+912T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47153952 | |||||||
| chr19:47154043 | G | A | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG00621.hp1 NA18949.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.527+1003G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47154043 | |||||||
| chr19:47154153 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.528-961C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47154153 | |||||||
| chr19:47154458 | AGAGGG | A | 6 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-654_528-650del others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154458 | ||||||
| chr19:47154480 | C | CT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0027 others(116): Show |
119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.528-604dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154480 | C | CTT | 19 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(16): Show |
19 | HG00621.hp2 HG00741.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.528-605_528-604dup others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154480 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.528-634C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47154480 | |||||||
| chr19:47154480 | CT | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0099 others(21): Show |
24 | HG00738.hp2 HG01168.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.528-604delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154480 | CTT | C | 20 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
20 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.528-605_528-604del others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154480 | CTTT | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(17): Show |
20 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.528-606_528-604del others(3): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154480 | CTTTT | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0232 others(63): Show |
66 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.528-607_528-604del others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154480 | CTTTTT | C | 7 | a0001c0001t0001g0224 a0001c0001t0001g0253 a0001c0001t0001g0300 others(4): Show |
7 | HG01257.hp2 HG02132.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.528-608_528-604del others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154480 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.528-615_528-604del others(12): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154480 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0078 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.528-617_528-604del others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 47154480 | ||||||
| chr19:47154646 | C | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0133 |
2 | NA18983.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.528-468C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47154646 | |||||||
| chr19:47154858 | T | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.528-256T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47154858 | |||||||
| chr19:47154867 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.528-247C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47154867 | |||||||
| chr19:47154941 | G | C | 1 | a0001c0001t0001g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.528-173G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47154941 | |||||||
| chr19:47155026 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0091 a0001c0001t0002g0094 others(4): Show |
7 | HG02809.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.528-88C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47155026 | |||||||
| chr19:47155063 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0092 others(86): Show |
89 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.528-51T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 4/8 | chr19 | 47155063 | |||||||
| chr19:47155225 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(85): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.627+12G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155225 | |||||||
| chr19:47155425 | T | C | 2 | a0001c0001t0001g0351 a0001c0001t0001g0353 |
2 | HG00597.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.627+212T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155425 | |||||||
| chr19:47155457 | A | C | 1 | a0001c0001t0001g0326 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.627+244A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155457 | |||||||
| chr19:47155469 | T | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0300 a0001c0001t0001g0304 others(2): Show |
5 | NA18963.hp2 NA18965.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+256T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155469 | |||||||
| chr19:47155499 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.627+286C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155499 | |||||||
| chr19:47155500 | G | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(56): Show |
59 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.627+287G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155500 | |||||||
| chr19:47155509 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.627+296G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155509 | |||||||
| chr19:47155630 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.627+417C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155630 | |||||||
| chr19:47155639 | A | G | 2 | a0001c0001t0001g0367 a0001c0001t0001g0373 |
2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.627+426A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155639 | |||||||
| chr19:47155705 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.627+492G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155705 | |||||||
| chr19:47155749 | C | CT | 26 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0093 others(23): Show |
26 | HG01106.hp2 HG01358.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.627+553dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47155749 | ||||||
| chr19:47155773 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.627+560G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155773 | |||||||
| chr19:47155774 | AGTCTTGC others(771): Show |
A | 1 | a0001c0001t0001g0013 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.627+716_627+1493de others(1): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47155774 | ||||||
| chr19:47155928 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.627+715A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155928 | |||||||
| chr19:47155982 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.627+769A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47155982 | |||||||
| chr19:47156035 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.627+822G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156035 | |||||||
| chr19:47156153 | G | T | 1 | a0001c0001t0005g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.627+940G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156153 | |||||||
| chr19:47156231 | A | G | 6 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | HG02056.hp1 NA19011.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.627+1018A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156231 | |||||||
| chr19:47156370 | T | G | 4 | a0002c0002t0001g0033 a0002c0002t0001g0044 a0002c0002t0001g0045 others(1): Show |
4 | HG02071.hp1 NA18957.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+1157T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156370 | |||||||
| chr19:47156378 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.627+1165C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156378 | |||||||
| chr19:47156389 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01261.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.627+1176G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156389 | |||||||
| chr19:47156432 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.627+1219C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156432 | |||||||
| chr19:47156440 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0091 a0001c0001t0002g0094 others(4): Show |
7 | HG02809.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+1227C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156440 | |||||||
| chr19:47156464 | C | T | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | HG02132.hp1 NA18960.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+1251C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156464 | |||||||
| chr19:47156468 | ACT | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+1258_627+1259d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47156468 | ||||||
| chr19:47156493 | T | G | 1 | a0001c0001t0005g0072 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.627+1280T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156493 | |||||||
| chr19:47156708 | G | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.627+1495G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156708 | |||||||
| chr19:47156904 | A | C | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.627+1691A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47156904 | |||||||
| chr19:47157708 | C | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0048 others(5): Show |
8 | HG02818.hp1 HG03017.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+2495C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47157708 | |||||||
| chr19:47157720 | C | T | 3 | a0001c0001t0001g0302 a0001c0001t0001g0307 a0001c0001t0001g0329 |
3 | HG00738.hp1 HG02738.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.627+2507C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47157720 | |||||||
| chr19:47157808 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.627+2595T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47157808 | |||||||
| chr19:47157877 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(85): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.627+2664G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47157877 | |||||||
| chr19:47157926 | A | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG02886.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+2713A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47157926 | |||||||
| chr19:47158032 | G | C | 1 | a0001c0001t0001g0346 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.627+2819G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158032 | |||||||
| chr19:47158236 | G | A | 16 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.627+3023G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158236 | |||||||
| chr19:47158458 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.627+3245G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158458 | |||||||
| chr19:47158516 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02647.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.627+3303G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158516 | |||||||
| chr19:47158598 | G | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(82): Show |
85 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.627+3385G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158598 | |||||||
| chr19:47158679 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.627+3466T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158679 | |||||||
| chr19:47158704 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG01081.hp2 HG01243.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.627+3491C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158704 | |||||||
| chr19:47158812 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.627+3599G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158812 | |||||||
| chr19:47158867 | A | AT | 5 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
5 | HG02647.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+3657dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47158867 | ||||||
| chr19:47158881 | A | T | 7 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0355 others(4): Show |
7 | HG00558.hp1 NA18952.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+3668A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47158881 | |||||||
| chr19:47159367 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.627+4154C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159367 | |||||||
| chr19:47159453 | C | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.627+4240C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159453 | |||||||
| chr19:47159459 | G | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(265): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.627+4246G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159459 | |||||||
| chr19:47159466 | A | C | 1 | a0001c0001t0001g0013 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.627+4253A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159466 | |||||||
| chr19:47159534 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
21 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.627+4321G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159534 | |||||||
| chr19:47159550 | CT | C | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+4352delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47159550 | ||||||
| chr19:47159578 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.627+4365G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159578 | |||||||
| chr19:47159578 | G | T | 1 | a0001c0001t0001g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.627+4365G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159578 | |||||||
| chr19:47159735 | C | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.627+4522C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159735 | |||||||
| chr19:47159798 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.627+4585A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47159798 | |||||||
| chr19:47160171 | G | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.627+4958G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160171 | |||||||
| chr19:47160178 | T | C | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+4965T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160178 | |||||||
| chr19:47160214 | A | AT | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(128): Show |
131 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.627+5026dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47160214 | ||||||
| chr19:47160214 | A | ATT | 115 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0024 others(112): Show |
115 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.627+5025_627+5026d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47160214 | ||||||
| chr19:47160214 | A | ATTT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0179 others(26): Show |
29 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.627+5024_627+5026d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47160214 | ||||||
| chr19:47160225 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.627+5012T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160225 | |||||||
| chr19:47160370 | C | A | 8 | a0001c0001t0001g0296 a0001c0001t0001g0300 a0001c0001t0001g0303 others(5): Show |
8 | NA18963.hp2 NA18965.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+5157C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160370 | |||||||
| chr19:47160388 | A | AT | 35 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0030 others(32): Show |
35 | HG00438.hp2 HG00621.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.627+5199dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47160388 | ||||||
| chr19:47160388 | AT | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.627+5199delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47160388 | ||||||
| chr19:47160388 | ATT | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0119 a0001c0001t0001g0133 others(4): Show |
7 | HG01192.hp2 HG02735.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+5198_627+5199d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47160388 | ||||||
| chr19:47160458 | G | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.627+5245G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160458 | |||||||
| chr19:47160475 | A | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0081 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+5262A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160475 | |||||||
| chr19:47160522 | G | A | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | NA18952.hp1 NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.627+5309G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160522 | |||||||
| chr19:47160546 | C | T | 3 | a0002c0002t0001g0033 a0002c0002t0001g0044 a0002c0002t0001g0045 |
3 | HG02071.hp1 NA18974.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.627+5333C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160546 | |||||||
| chr19:47160586 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.627+5373G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160586 | |||||||
| chr19:47160597 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.627+5384G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160597 | |||||||
| chr19:47160616 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.627+5403C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160616 | |||||||
| chr19:47160674 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.627+5461C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160674 | |||||||
| chr19:47160686 | T | C | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+5473T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47160686 | |||||||
| chr19:47161098 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.627+5885C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47161098 | |||||||
| chr19:47161182 | G | GT | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(269): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.627+5984dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47161182 | ||||||
| chr19:47161182 | G | GTT | 9 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0114 others(6): Show |
9 | HG00597.hp1 HG01123.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+5983_627+5984d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47161182 | ||||||
| chr19:47161301 | G | A | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+6088G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47161301 | |||||||
| chr19:47161395 | G | A | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+6182G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47161395 | |||||||
| chr19:47161580 | G | A | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+6367G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47161580 | |||||||
| chr19:47161694 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
21 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.627+6481T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47161694 | |||||||
| chr19:47161749 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0092 others(86): Show |
89 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.627+6536T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47161749 | |||||||
| chr19:47161897 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.627+6684C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47161897 | |||||||
| chr19:47162100 | A | G | 5 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0001g0177 others(2): Show |
5 | NA18984.hp1 NA19000.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+6887A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47162100 | |||||||
| chr19:47162489 | G | GT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0175 others(4): Show |
7 | HG00438.hp1 HG01261.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+7284dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47162489 | ||||||
| chr19:47162680 | T | C | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-7138T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47162680 | |||||||
| chr19:47162862 | C | T | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-6956C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47162862 | |||||||
| chr19:47163096 | C | T | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-6722C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163096 | |||||||
| chr19:47163114 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.628-6704T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163114 | |||||||
| chr19:47163251 | C | CA | 7 | a0001c0001t0001g0090 a0001c0001t0001g0211 a0001c0001t0001g0212 others(4): Show |
7 | HG01358.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-6554dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47163251 | ||||||
| chr19:47163265 | GAA | G | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-6550_628-6549d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47163265 | ||||||
| chr19:47163454 | G | A | 14 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(11): Show |
14 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.628-6364G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163454 | |||||||
| chr19:47163470 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.628-6348G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163470 | |||||||
| chr19:47163687 | G | A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-6131G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163687 | |||||||
| chr19:47163692 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.628-6126A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163692 | |||||||
| chr19:47163717 | ACT | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0051 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-6098_628-6097d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47163717 | ||||||
| chr19:47163722 | A | G | 1 | a0001c0001t0001g0359 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.628-6096A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163722 | |||||||
| chr19:47163726 | C | G | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-6092C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163726 | |||||||
| chr19:47163838 | C | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
21 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.628-5980C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163838 | |||||||
| chr19:47163845 | G | A | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-5973G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163845 | |||||||
| chr19:47163894 | C | G | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-5924C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47163894 | |||||||
| chr19:47164069 | T | A | 14 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(11): Show |
14 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.628-5749T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164069 | |||||||
| chr19:47164138 | C | T | 1 | a0001c0001t0009g0164 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.628-5680C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164138 | |||||||
| chr19:47164237 | C | T | 6 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01261.hp1 HG02615.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-5581C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164237 | |||||||
| chr19:47164253 | C | G | 6 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01261.hp1 HG02615.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-5565C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164253 | |||||||
| chr19:47164270 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.628-5548G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164270 | |||||||
| chr19:47164342 | G | C | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.628-5476G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164342 | |||||||
| chr19:47164377 | T | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG02109.hp1 NA18940.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-5441T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164377 | |||||||
| chr19:47164389 | C | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.628-5429C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164389 | |||||||
| chr19:47164394 | G | C | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.628-5424G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164394 | |||||||
| chr19:47164403 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0091 a0001c0001t0002g0265 others(2): Show |
5 | HG02809.hp2 HG03579.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-5415G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164403 | |||||||
| chr19:47164447 | A | G | 7 | a0001c0001t0001g0119 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
7 | HG00738.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-5371A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164447 | |||||||
| chr19:47164501 | TCCTCTTC others(43): Show |
T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5316_628-5267d others(52): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164501 | |||||||
| chr19:47164539 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.628-5279C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164539 | |||||||
| chr19:47164554 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5264T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164554 | |||||||
| chr19:47164557 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5261T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164557 | |||||||
| chr19:47164558 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5260T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164558 | |||||||
| chr19:47164567 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5251T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164567 | |||||||
| chr19:47164572 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5246T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164572 | |||||||
| chr19:47164573 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5245T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164573 | |||||||
| chr19:47164586 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5232A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164586 | |||||||
| chr19:47164587 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5231A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164587 | |||||||
| chr19:47164588 | A | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5230A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164588 | |||||||
| chr19:47164592 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5226C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164592 | |||||||
| chr19:47164593 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5225T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164593 | |||||||
| chr19:47164595 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5223C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164595 | |||||||
| chr19:47164597 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5221G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164597 | |||||||
| chr19:47164600 | A | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5218A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164600 | |||||||
| chr19:47164601 | A | T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5217A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164601 | |||||||
| chr19:47164602 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5216C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164602 | |||||||
| chr19:47164603 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5215A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164603 | |||||||
| chr19:47164607 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5211T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164607 | |||||||
| chr19:47164612 | G | T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5206G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164612 | |||||||
| chr19:47164614 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5204T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164614 | |||||||
| chr19:47164615 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5203T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164615 | |||||||
| chr19:47164616 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5202G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164616 | |||||||
| chr19:47164621 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5197G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164621 | |||||||
| chr19:47164623 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5195T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164623 | |||||||
| chr19:47164627 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5191T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164627 | |||||||
| chr19:47164631 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5187G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164631 | |||||||
| chr19:47164635 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5183T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164635 | |||||||
| chr19:47164637 | ACCTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5180_628-5168d others(15): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164637 | |||||||
| chr19:47164639 | C | CT | 47 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0035 others(44): Show |
47 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.628-5152dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47164639 | ||||||
| chr19:47164639 | C | CTT | 47 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0030 others(44): Show |
47 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.628-5153_628-5152d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47164639 | ||||||
| chr19:47164639 | C | CTTT | 15 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0134 others(12): Show |
15 | HG00621.hp2 HG01243.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.628-5154_628-5152d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47164639 | ||||||
| chr19:47164639 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.628-5162_628-5152d others(13): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47164639 | ||||||
| chr19:47164639 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0011t0001g0343 |
3 | HG02109.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-5163_628-5152d others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47164639 | ||||||
| chr19:47164639 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0279 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.628-5164_628-5152d others(15): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47164639 | ||||||
| chr19:47164639 | CT | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0050 a0001c0001t0001g0059 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.628-5152delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47164639 | ||||||
| chr19:47164639 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0349 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.628-5162_628-5152d others(13): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47164639 | ||||||
| chr19:47164654 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5164T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164654 | |||||||
| chr19:47164656 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5162T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164656 | |||||||
| chr19:47164662 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5156T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164662 | |||||||
| chr19:47164663 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5155T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164663 | |||||||
| chr19:47164664 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5154T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164664 | |||||||
| chr19:47164665 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5153T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164665 | |||||||
| chr19:47164666 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5152T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164666 | |||||||
| chr19:47164667 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5151G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164667 | |||||||
| chr19:47164669 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5149G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164669 | |||||||
| chr19:47164671 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5147C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164671 | |||||||
| chr19:47164674 | A | T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5144A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164674 | |||||||
| chr19:47164675 | G | T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5143G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164675 | |||||||
| chr19:47164676 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5142T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164676 | |||||||
| chr19:47164678 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5140T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164678 | |||||||
| chr19:47164681 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5137C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164681 | |||||||
| chr19:47164683 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5135C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164683 | |||||||
| chr19:47164684 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5134T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164684 | |||||||
| chr19:47164685 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5133G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164685 | |||||||
| chr19:47164686 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5132T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164686 | |||||||
| chr19:47164690 | C | CACACCAC others(66): Show |
1 | a0001c0001t0001g0011 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-5128_628-5127i others(75): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164690 | |||||||
| chr19:47164894 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.628-4924C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164894 | |||||||
| chr19:47164941 | A | C | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-4877A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47164941 | |||||||
| chr19:47165014 | A | T | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-4804A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165014 | |||||||
| chr19:47165035 | T | C | 1 | a0001c0001t0009g0164 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.628-4783T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165035 | |||||||
| chr19:47165076 | C | CT | 116 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0017 others(113): Show |
116 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.628-4717dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47165076 | ||||||
| chr19:47165076 | C | CTT | 27 | a0001c0001t0001g0005 a0001c0001t0001g0096 a0001c0001t0001g0114 others(24): Show |
27 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.628-4718_628-4717d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47165076 | ||||||
| chr19:47165076 | C | CTTT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0001g0109 others(4): Show |
7 | HG01884.hp2 HG02602.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-4719_628-4717d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47165076 | ||||||
| chr19:47165076 | CT | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0206 others(85): Show |
88 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.628-4717delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47165076 | ||||||
| chr19:47165120 | C | G | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-4698C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165120 | |||||||
| chr19:47165194 | A | G | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-4624A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165194 | |||||||
| chr19:47165209 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.628-4609C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165209 | |||||||
| chr19:47165251 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.628-4567G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165251 | |||||||
| chr19:47165297 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.628-4521C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165297 | |||||||
| chr19:47165322 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.628-4496T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165322 | |||||||
| chr19:47165408 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.628-4410A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165408 | |||||||
| chr19:47165659 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA19077.hp1 NA19078.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.628-4159G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47165659 | |||||||
| chr19:47166107 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.628-3711T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166107 | |||||||
| chr19:47166177 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.628-3641G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166177 | |||||||
| chr19:47166180 | G | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0058 others(5): Show |
8 | HG02027.hp2 HG02056.hp1 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-3638G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166180 | |||||||
| chr19:47166202 | G | A | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-3616G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166202 | |||||||
| chr19:47166221 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0080 others(4): Show |
7 | HG02559.hp1 HG02896.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-3597G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166221 | |||||||
| chr19:47166345 | A | G | 1 | a0001c0001t0002g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.628-3473A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166345 | |||||||
| chr19:47166380 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(56): Show |
59 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.628-3438G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166380 | |||||||
| chr19:47166632 | CAA | C | 5 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
5 | HG02647.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-3184_628-3183d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47166632 | ||||||
| chr19:47166862 | G | A | 2 | a0001c0001t0001g0318 a0001c0001t0001g0340 |
2 | NA18964.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.628-2956G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166862 | |||||||
| chr19:47166978 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.628-2840G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47166978 | |||||||
| chr19:47167011 | G | A | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-2807G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167011 | |||||||
| chr19:47167113 | A | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0234 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628-2705A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167113 | |||||||
| chr19:47167121 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.628-2697T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167121 | |||||||
| chr19:47167196 | C | T | 1 | a0001c0001t0001g0348 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.628-2622C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167196 | |||||||
| chr19:47167364 | C | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0106 others(6): Show |
9 | HG01261.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.628-2454C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167364 | |||||||
| chr19:47167396 | C | T | 4 | a0001c0001t0002g0006 a0001c0001t0002g0094 a0001c0001t0002g0265 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-2422C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167396 | |||||||
| chr19:47167426 | G | A | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-2392G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167426 | |||||||
| chr19:47167443 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.628-2375T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167443 | |||||||
| chr19:47167519 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.628-2299T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167519 | |||||||
| chr19:47167529 | T | C | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG01081.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.628-2289T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167529 | |||||||
| chr19:47167533 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02647.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-2285C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167533 | |||||||
| chr19:47167650 | T | C | 22 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.628-2168T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167650 | |||||||
| chr19:47167784 | A | G | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-2034A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167784 | |||||||
| chr19:47167930 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.628-1888C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167930 | |||||||
| chr19:47167946 | A | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.628-1872A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47167946 | |||||||
| chr19:47168123 | A | G | 7 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-1695A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47168123 | |||||||
| chr19:47168192 | G | GA | 23 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
23 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.628-1616dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47168192 | ||||||
| chr19:47168223 | T | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0322 |
2 | HG00735.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.628-1595T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47168223 | |||||||
| chr19:47168451 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.628-1367A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47168451 | |||||||
| chr19:47168496 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02647.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-1322G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47168496 | |||||||
| chr19:47168511 | A | C | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02109.hp1 HG02647.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-1307A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47168511 | |||||||
| chr19:47168600 | GTGT | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG03017.hp1 HG03704.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-1204_628-1202d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 47168600 | ||||||
| chr19:47168809 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.628-1009G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47168809 | |||||||
| chr19:47169194 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0223 |
3 | HG02572.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.628-624C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47169194 | |||||||
| chr19:47169309 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.628-509G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47169309 | |||||||
| chr19:47169439 | T | A | 1 | a0001c0001t0001g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.628-379T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47169439 | |||||||
| chr19:47169518 | T | C | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.628-300T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47169518 | |||||||
| chr19:47169529 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.628-289C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 5/8 | chr19 | 47169529 | |||||||
| chr19:47170125 | C | G | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.733+202C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47170125 | |||||||
| chr19:47170172 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.733+249G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47170172 | |||||||
| chr19:47170300 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+377C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47170300 | |||||||
| chr19:47170503 | C | CT | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(178): Show |
181 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.733+601dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47170503 | ||||||
| chr19:47170503 | C | CTT | 20 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0058 others(17): Show |
20 | HG01981.hp1 HG02027.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.733+600_733+601dup others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47170503 | ||||||
| chr19:47170593 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0050 |
3 | HG02818.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.733+670A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47170593 | |||||||
| chr19:47170598 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG03017.hp1 HG03704.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+675C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47170598 | |||||||
| chr19:47170641 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.733+718G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47170641 | |||||||
| chr19:47171264 | C | T | 2 | a0001c0001t0001g0359 a0001c0001t0001g0377 |
2 | HG02040.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.733+1341C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171264 | |||||||
| chr19:47171359 | T | A | 1 | a0001c0001t0001g0014 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.733+1436T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171359 | |||||||
| chr19:47171495 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.733+1572G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171495 | |||||||
| chr19:47171561 | C | T | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.733+1638C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171561 | |||||||
| chr19:47171608 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+1685C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171608 | |||||||
| chr19:47171710 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+1787C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171710 | |||||||
| chr19:47171712 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.733+1789C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171712 | |||||||
| chr19:47171720 | T | C | 4 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG02886.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+1797T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171720 | |||||||
| chr19:47171942 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+2019C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47171942 | |||||||
| chr19:47172012 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+2089C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172012 | |||||||
| chr19:47172105 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.733+2182A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172105 | |||||||
| chr19:47172171 | G | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+2248G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172171 | |||||||
| chr19:47172354 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.733+2431A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172354 | |||||||
| chr19:47172358 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+2435G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172358 | |||||||
| chr19:47172429 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+2506C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172429 | |||||||
| chr19:47172563 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0223 |
3 | HG02572.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.733+2640A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172563 | |||||||
| chr19:47172750 | T | A | 23 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(20): Show |
23 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.733+2827T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172750 | |||||||
| chr19:47172778 | AAG | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
8 | HG01074.hp1 HG02559.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.733+2859_733+2860d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47172778 | ||||||
| chr19:47172807 | A | G | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+2884A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172807 | |||||||
| chr19:47172808 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0322 |
2 | HG00735.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.733+2885C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172808 | |||||||
| chr19:47172809 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(18): Show |
21 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.733+2886G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172809 | |||||||
| chr19:47172833 | G | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(85): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.733+2910G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172833 | |||||||
| chr19:47172842 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.733+2919C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172842 | |||||||
| chr19:47172843 | G | A | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.733+2920G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172843 | |||||||
| chr19:47172905 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+2982C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172905 | |||||||
| chr19:47172908 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.733+2985C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172908 | |||||||
| chr19:47172921 | G | T | 1 | a0001c0001t0001g0278 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.733+2998G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47172921 | |||||||
| chr19:47173002 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0123 a0001c0001t0001g0180 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.733+3079G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173002 | |||||||
| chr19:47173062 | T | G | 6 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+3139T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173062 | |||||||
| chr19:47173154 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733+3231A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173154 | |||||||
| chr19:47173199 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733+3276G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173199 | |||||||
| chr19:47173359 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.733+3436T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173359 | |||||||
| chr19:47173363 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01496.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.733+3440C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173363 | |||||||
| chr19:47173835 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0047 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.733+3912A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173835 | |||||||
| chr19:47173894 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG00733.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.733+3971C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173894 | |||||||
| chr19:47173974 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+4051C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47173974 | |||||||
| chr19:47174081 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+4158G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174081 | |||||||
| chr19:47174299 | C | CT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0101 others(5): Show |
8 | HG00741.hp1 HG01257.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.733+4391dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47174299 | ||||||
| chr19:47174300 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.733+4377T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174300 | |||||||
| chr19:47174347 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.733+4424C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174347 | |||||||
| chr19:47174382 | A | C | 2 | a0001c0001t0001g0310 a0001c0001t0001g0320 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.733+4459A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174382 | |||||||
| chr19:47174460 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.733+4537G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174460 | |||||||
| chr19:47174466 | G | A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+4543G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174466 | |||||||
| chr19:47174506 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.733+4583C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174506 | |||||||
| chr19:47174548 | C | T | 8 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(5): Show |
8 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.733+4625C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174548 | |||||||
| chr19:47174563 | A | AT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0058 others(107): Show |
110 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.733+4665dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47174563 | ||||||
| chr19:47174563 | A | ATT | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(49): Show |
52 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.733+4664_733+4665d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47174563 | ||||||
| chr19:47174563 | A | ATTT | 14 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0100 others(11): Show |
14 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.733+4663_733+4665d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47174563 | ||||||
| chr19:47174589 | G | T | 1 | a0002c0002t0001g0070 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.733+4666G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174589 | |||||||
| chr19:47174603 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG00738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.733+4680C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174603 | |||||||
| chr19:47174612 | T | G | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.733+4689T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174612 | |||||||
| chr19:47174675 | C | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG02886.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+4752C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174675 | |||||||
| chr19:47174697 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.733+4774C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174697 | |||||||
| chr19:47174734 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.733+4811G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174734 | |||||||
| chr19:47174795 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+4872G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174795 | |||||||
| chr19:47174838 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.733+4915G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174838 | |||||||
| chr19:47174897 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+4974C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47174897 | |||||||
| chr19:47175010 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.733+5087T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175010 | |||||||
| chr19:47175107 | A | AT | 155 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(152): Show |
155 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.733+5208dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47175107 | ||||||
| chr19:47175107 | A | ATT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(21): Show |
24 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.733+5207_733+5208d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47175107 | ||||||
| chr19:47175107 | AT | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0053 others(5): Show |
8 | HG00597.hp2 HG01168.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.733+5208delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47175107 | ||||||
| chr19:47175155 | G | A | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0003g0003 others(3): Show |
6 | HG00738.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+5232G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175155 | |||||||
| chr19:47175472 | T | C | 7 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0106 others(4): Show |
7 | HG01261.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+5549T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175472 | |||||||
| chr19:47175609 | A | G | 1 | a0001c0001t0001g0366 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.733+5686A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175609 | |||||||
| chr19:47175688 | G | T | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02818.hp2 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+5765G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175688 | |||||||
| chr19:47175771 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.733+5848T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175771 | |||||||
| chr19:47175806 | T | A | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | NA18952.hp1 NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.733+5883T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175806 | |||||||
| chr19:47175821 | C | G | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+5898C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175821 | |||||||
| chr19:47175945 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.733+6022G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47175945 | |||||||
| chr19:47176039 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.733+6116A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47176039 | |||||||
| chr19:47176044 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+6121C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47176044 | |||||||
| chr19:47176259 | C | G | 1 | a0001c0001t0001g0246 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.733+6336C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47176259 | |||||||
| chr19:47176541 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(277): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.733+6618T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47176541 | |||||||
| chr19:47176665 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0191 |
2 | NA18992.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.733+6742C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47176665 | |||||||
| chr19:47176768 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0191 |
2 | NA18992.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.733+6845C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47176768 | |||||||
| chr19:47176823 | A | G | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0003g0003 others(3): Show |
6 | HG00738.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+6900A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47176823 | |||||||
| chr19:47176878 | G | A | 2 | a0001c0001t0001g0208 a0001c0006t0001g0210 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.733+6955G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47176878 | |||||||
| chr19:47177296 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+7373C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47177296 | |||||||
| chr19:47177362 | T | G | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0003g0003 others(3): Show |
6 | HG00738.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+7439T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47177362 | |||||||
| chr19:47177369 | T | C | 5 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
5 | HG02647.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+7446T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47177369 | |||||||
| chr19:47177423 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+7500A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47177423 | |||||||
| chr19:47177529 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.733+7606A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47177529 | |||||||
| chr19:47177554 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.733+7631G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47177554 | |||||||
| chr19:47177851 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.733+7928G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47177851 | |||||||
| chr19:47178114 | G | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0109 a0001c0001t0001g0113 others(10): Show |
13 | HG00741.hp1 HG01123.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.733+8191G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47178114 | |||||||
| chr19:47178210 | TC | T | 109 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
109 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.733+8289delC | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47178210 | ||||||
| chr19:47178221 | G | A | 22 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.733+8298G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47178221 | |||||||
| chr19:47178231 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.733+8308G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47178231 | |||||||
| chr19:47178306 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.733+8383C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47178306 | |||||||
| chr19:47179020 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.733+9097C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179020 | |||||||
| chr19:47179075 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0092 others(102): Show |
105 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.733+9152T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179075 | |||||||
| chr19:47179124 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.733+9201A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179124 | |||||||
| chr19:47179158 | C | G | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0003g0003 others(3): Show |
6 | HG00738.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+9235C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179158 | |||||||
| chr19:47179192 | C | CA | 19 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0029 others(16): Show |
19 | HG00738.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.733+9285dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47179192 | ||||||
| chr19:47179244 | G | A | 2 | a0001c0001t0004g0098 a0001c0001t0004g0273 |
2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.733+9321G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179244 | |||||||
| chr19:47179274 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0092 others(102): Show |
105 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.733+9351A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179274 | |||||||
| chr19:47179323 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(147): Show |
150 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.733+9400T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179323 | |||||||
| chr19:47179336 | T | C | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+9413T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179336 | |||||||
| chr19:47179501 | G | GA | 7 | a0001c0001t0001g0288 a0001c0001t0001g0337 a0001c0001t0002g0091 others(4): Show |
7 | HG02109.hp1 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+9591dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47179501 | ||||||
| chr19:47179501 | GA | G | 7 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0355 others(4): Show |
7 | HG00558.hp1 NA18952.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+9591delA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47179501 | ||||||
| chr19:47179507 | A | T | 1 | a0001c0001t0001g0330 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.733+9584A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179507 | |||||||
| chr19:47179764 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.733+9841T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47179764 | |||||||
| chr19:47179910 | GTTC | G | 10 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01515.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+9992_733+9994d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47179910 | ||||||
| chr19:47180143 | T | G | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+10220T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47180143 | |||||||
| chr19:47180377 | C | G | 1 | a0001c0001t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.733+10454C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47180377 | |||||||
| chr19:47180540 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.733+10617G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47180540 | |||||||
| chr19:47180827 | G | A | 42 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0136 others(39): Show |
42 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.733+10904G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47180827 | |||||||
| chr19:47180829 | A | C | 4 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(1): Show |
4 | HG00544.hp2 NA18954.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+10906A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47180829 | |||||||
| chr19:47180834 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.733+10911C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47180834 | |||||||
| chr19:47181107 | G | A | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.733+11184G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181107 | |||||||
| chr19:47181144 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
22 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.733+11221C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181144 | |||||||
| chr19:47181146 | A | G | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.733+11223A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181146 | |||||||
| chr19:47181162 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.733+11239C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181162 | |||||||
| chr19:47181248 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.733+11325G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181248 | |||||||
| chr19:47181388 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.733+11465C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181388 | |||||||
| chr19:47181476 | C | CT | 9 | a0001c0001t0001g0079 a0001c0001t0001g0114 a0001c0001t0001g0121 others(6): Show |
9 | HG00735.hp1 HG01981.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.733+11573dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47181476 | ||||||
| chr19:47181476 | CT | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(196): Show |
199 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.733+11573delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47181476 | ||||||
| chr19:47181481 | T | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0308 a0001c0001t0001g0309 others(6): Show |
9 | HG00438.hp1 NA18945.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+11558T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181481 | |||||||
| chr19:47181517 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.733+11594C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181517 | |||||||
| chr19:47181556 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.733+11633G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181556 | |||||||
| chr19:47181586 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.733+11663C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181586 | |||||||
| chr19:47181723 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.733+11800C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181723 | |||||||
| chr19:47181780 | C | CT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(87): Show |
90 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.733+11878dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47181780 | ||||||
| chr19:47181780 | CT | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.733+11878delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47181780 | ||||||
| chr19:47181780 | CTT | C | 21 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0001g0236 others(18): Show |
21 | HG00621.hp1 HG01069.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.733+11877_733+1187 others(6): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47181780 | ||||||
| chr19:47181813 | AT | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0051 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+11904delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47181813 | ||||||
| chr19:47181899 | A | G | 1 | a0001c0001t0002g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.733+11976A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181899 | |||||||
| chr19:47181966 | T | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0333 |
2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.733+12043T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47181966 | |||||||
| chr19:47182037 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.733+12114C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182037 | |||||||
| chr19:47182132 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.733+12209C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182132 | |||||||
| chr19:47182319 | C | A | 1 | a0001c0001t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.733+12396C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182319 | |||||||
| chr19:47182461 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(98): Show |
101 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.733+12538C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182461 | |||||||
| chr19:47182462 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+12539G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182462 | |||||||
| chr19:47182463 | T | G | 1 | a0001c0001t0001g0319 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+12540T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182463 | |||||||
| chr19:47182464 | A | AGT | 41 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0001g0137 others(38): Show |
41 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.733+12573_733+1257 others(6): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | A | AGTGT | 12 | a0001c0001t0001g0123 a0001c0001t0001g0152 a0001c0001t0001g0161 others(9): Show |
12 | HG00280.hp1 HG01361.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.733+12571_733+1257 others(8): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | A | AGTGTGT | 31 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0092 others(28): Show |
31 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.733+12569_733+1257 others(10): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | A | AGTGTGTG others(1): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0149 a0001c0001t0001g0224 others(7): Show |
10 | HG00735.hp2 HG01168.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+12567_733+1257 others(12): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | A | AGTGTGTG others(3): Show |
16 | a0001c0001t0001g0093 a0001c0001t0001g0122 a0001c0001t0001g0232 others(13): Show |
16 | HG01106.hp2 HG02132.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.733+12565_733+1257 others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | A | AGTGTGTG others(5): Show |
3 | a0001c0001t0001g0246 a0001c0001t0001g0250 a0001c0001t0001g0259 |
3 | NA18962.hp2 NA18999.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.733+12563_733+1257 others(16): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | A | AGTGTGTG others(7): Show |
2 | a0001c0001t0001g0242 a0001c0001t0001g0256 |
2 | HG01433.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.733+12561_733+1257 others(18): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | A | AGTGTGTG others(9): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0342 |
2 | HG01433.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.733+12559_733+1257 others(20): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | A | T | 1 | a0001c0001t0001g0319 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+12541A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182464 | |||||||
| chr19:47182464 | AGT | A | 29 | a0001c0001t0001g0080 a0001c0001t0001g0097 a0001c0001t0001g0099 others(26): Show |
29 | HG00280.hp2 HG00741.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.733+12573_733+1257 others(6): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | AGTGT | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG00438.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+12571_733+1257 others(8): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | AGTGTGT | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG02809.hp2 HG02818.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+12569_733+1257 others(10): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | AGTGTGTG others(1): Show |
A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+12567_733+1257 others(12): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.733+12561_733+1257 others(18): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182464 | AGTGTGTG others(9): Show |
A | 2 | a0001c0001t0001g0028 a0001c0011t0001g0343 |
2 | HG02109.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.733+12559_733+1257 others(20): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182464 | ||||||
| chr19:47182488 | TGTGTGTG others(13): Show |
T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+12567_733+1258 others(24): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182488 | ||||||
| chr19:47182494 | T | C | 11 | a0001c0001t0001g0049 a0001c0001t0001g0268 a0001c0001t0001g0269 others(8): Show |
11 | HG02280.hp2 HG02723.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.733+12571T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182494 | |||||||
| chr19:47182494 | T | TGC | 3 | a0001c0001t0001g0048 a0001c0001t0001g0294 a0002c0002t0001g0063 |
3 | HG02818.hp1 NA18942.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.733+12572_733+1257 others(6): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182494 | ||||||
| chr19:47182496 | T | C | 66 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(63): Show |
66 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.733+12573T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182496 | |||||||
| chr19:47182496 | T | TGC | 38 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0040 others(35): Show |
38 | HG01168.hp2 HG01169.hp2 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.733+12578_733+1257 others(6): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGCGC | 10 | a0001c0001t0001g0035 a0001c0001t0001g0212 a0001c0001t0001g0213 others(7): Show |
10 | HG00733.hp2 HG02055.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+12576_733+1257 others(8): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGC | 16 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0043 others(13): Show |
16 | HG01070.hp2 HG01074.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.733+12574_733+1257 others(8): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGCGC | 10 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0001g0206 others(7): Show |
10 | HG01243.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+12574_733+1257 others(10): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGC | 5 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0151 others(2): Show |
5 | HG00558.hp2 HG01256.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+12574_733+1257 others(10): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGCG others(3): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0031 |
2 | HG01069.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.733+12574_733+1257 others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.733+12574_733+1257 others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0191 |
3 | NA18966.hp1 NA18992.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.733+12574_733+1257 others(16): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0229 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.733+12574_733+1257 others(18): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(3): Show |
2 | a0001c0001t0001g0254 a0001c0001t0001g0311 |
2 | NA18941.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.733+12574_733+1257 others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0205 |
2 | HG00738.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.733+12574_733+1257 others(16): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0017 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.733+12574_733+1257 others(18): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(5): Show |
1 | a0006c0007t0001g0244 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.733+12574_733+1257 others(16): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733+12574_733+1257 others(18): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0101 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.733+12574_733+1257 others(20): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(11): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0102 |
3 | NA18983.hp2 NA18985.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.733+12574_733+1257 others(22): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0100 a0001c0001t0001g0103 |
2 | HG02293.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.733+12574_733+1257 others(22): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(13): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0025 |
3 | HG01257.hp1 NA18986.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.733+12574_733+1257 others(24): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(16): Show |
1 | a0001c0001t0001g0197 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.733+12574_733+1257 others(27): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0021 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.733+12574_733+1257 others(30): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | T | TGTGTGTG others(23): Show |
1 | a0001c0001t0001g0020 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.733+12574_733+1257 others(34): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182496 | TGCGCGCA others(7): Show |
T | 1 | a0002c0002t0001g0033 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.733+12580_733+1259 others(18): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47182496 | ||||||
| chr19:47182498 | C | T | 9 | a0001c0001t0001g0225 a0001c0001t0001g0297 a0001c0001t0001g0298 others(6): Show |
9 | HG00544.hp2 HG04184.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+12575C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182498 | |||||||
| chr19:47182499 | G | GTGTGTGC others(4): Show |
1 | a0007c0009t0001g0241 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.733+12576_733+1257 others(15): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182499 | |||||||
| chr19:47182505 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.733+12582G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182505 | |||||||
| chr19:47182507 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0191 |
2 | NA18992.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.733+12584A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182507 | |||||||
| chr19:47182514 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.733+12591C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182514 | |||||||
| chr19:47182514 | C | T | 25 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(22): Show |
25 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.733+12591C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182514 | |||||||
| chr19:47182519 | A | G | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733+12596A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47182519 | |||||||
| chr19:47183013 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.733+13090T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47183013 | |||||||
| chr19:47183637 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.734-13596C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47183637 | |||||||
| chr19:47183730 | C | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-13503C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47183730 | |||||||
| chr19:47183803 | A | C | 1 | a0001c0001t0001g0342 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.734-13430A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47183803 | |||||||
| chr19:47183865 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.734-13368C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47183865 | |||||||
| chr19:47184074 | T | G | 45 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
45 | HG00733.hp2 HG01069.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.734-13159T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184074 | |||||||
| chr19:47184236 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-12997G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184236 | |||||||
| chr19:47184371 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.734-12862A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184371 | |||||||
| chr19:47184403 | G | T | 1 | a0007c0009t0001g0241 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.734-12830G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184403 | |||||||
| chr19:47184404 | T | G | 1 | a0007c0009t0001g0241 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.734-12829T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184404 | |||||||
| chr19:47184502 | C | T | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.734-12731C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184502 | |||||||
| chr19:47184642 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.734-12591C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184642 | |||||||
| chr19:47184677 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.734-12556C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184677 | |||||||
| chr19:47184753 | T | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.734-12480T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184753 | |||||||
| chr19:47184756 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.734-12477A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184756 | |||||||
| chr19:47184777 | G | T | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG01081.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.734-12456G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184777 | |||||||
| chr19:47184798 | T | TTTTTG | 8 | a0001c0001t0001g0123 a0001c0001t0001g0137 a0001c0001t0001g0147 others(5): Show |
8 | HG01361.hp1 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-12395_734-1239 others(9): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47184798 | ||||||
| chr19:47184798 | TTTTTG | T | 194 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(191): Show |
194 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(191): Show |
intron_variant | MODIFIER | c.734-12395_734-1239 others(9): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47184798 | ||||||
| chr19:47184798 | TTTTTGTT others(3): Show |
T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0107 a0001c0001t0002g0094 others(5): Show |
8 | HG01261.hp1 HG02027.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-12400_734-1239 others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47184798 | ||||||
| chr19:47184971 | C | G | 1 | a0001c0001t0001g0013 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.734-12262C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47184971 | |||||||
| chr19:47185067 | G | T | 2 | a0001c0001t0001g0096 a0001c0001t0007g0148 |
2 | HG00544.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.734-12166G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185067 | |||||||
| chr19:47185139 | A | G | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.734-12094A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185139 | |||||||
| chr19:47185233 | T | C | 1 | a0001c0001t0001g0365 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.734-12000T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185233 | |||||||
| chr19:47185240 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-11993A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185240 | |||||||
| chr19:47185362 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.734-11871C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185362 | |||||||
| chr19:47185413 | T | G | 1 | a0001c0001t0001g0282 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.734-11820T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185413 | |||||||
| chr19:47185634 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.734-11599C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185634 | |||||||
| chr19:47185910 | C | G | 1 | a0001c0001t0002g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734-11323C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185910 | |||||||
| chr19:47185988 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.734-11245C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47185988 | |||||||
| chr19:47186070 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.734-11163T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186070 | |||||||
| chr19:47186079 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.734-11154A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186079 | |||||||
| chr19:47186166 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.734-11067G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186166 | |||||||
| chr19:47186180 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.734-11053C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186180 | |||||||
| chr19:47186251 | T | TA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(93): Show |
96 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.734-10972dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47186251 | ||||||
| chr19:47186259 | A | AT | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-10974_734-1097 others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186259 | |||||||
| chr19:47186287 | G | GGATTTGG others(8): Show |
1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-10937_734-1092 others(19): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47186287 | ||||||
| chr19:47186320 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(144): Show |
147 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.734-10913T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186320 | |||||||
| chr19:47186322 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.734-10911G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186322 | |||||||
| chr19:47186440 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(95): Show |
98 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.734-10793G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186440 | |||||||
| chr19:47186507 | G | A | 24 | a0001c0001t0001g0012 a0001c0001t0001g0203 a0001c0001t0001g0204 others(21): Show |
24 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.734-10726G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186507 | |||||||
| chr19:47186656 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0051 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-10577C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186656 | |||||||
| chr19:47186664 | C | G | 99 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
99 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.734-10569C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186664 | |||||||
| chr19:47186672 | C | G | 3 | a0001c0001t0001g0301 a0001c0001t0001g0317 a0001c0001t0001g0341 |
3 | HG01928.hp2 HG02004.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.734-10561C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186672 | |||||||
| chr19:47186684 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0222 |
2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.734-10549A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186684 | |||||||
| chr19:47186779 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-10454G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186779 | |||||||
| chr19:47186828 | G | GTC | 3 | a0001c0001t0002g0006 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02809.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.734-10403_734-1040 others(6): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47186828 | ||||||
| chr19:47186899 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.734-10334G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47186899 | |||||||
| chr19:47187026 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.734-10207G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47187026 | |||||||
| chr19:47187181 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-10052G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47187181 | |||||||
| chr19:47187258 | T | C | 7 | a0001c0001t0001g0040 a0001c0001t0001g0053 a0001c0001t0001g0058 others(4): Show |
7 | HG02027.hp2 HG02056.hp1 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-9975T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47187258 | |||||||
| chr19:47187554 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(95): Show |
98 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.734-9679G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47187554 | |||||||
| chr19:47187767 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.734-9466T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47187767 | |||||||
| chr19:47187960 | G | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG00738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.734-9273G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47187960 | |||||||
| chr19:47188210 | G | C | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-9023G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47188210 | |||||||
| chr19:47188349 | CA | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(255): Show |
258 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.734-8872delA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47188349 | ||||||
| chr19:47188537 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA19077.hp1 NA19078.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.734-8696C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47188537 | |||||||
| chr19:47188580 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.734-8653T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47188580 | |||||||
| chr19:47188613 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.734-8620C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47188613 | |||||||
| chr19:47189111 | C | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.734-8122C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189111 | |||||||
| chr19:47189147 | G | A | 8 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0048 others(5): Show |
8 | HG02818.hp1 HG03017.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-8086G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189147 | |||||||
| chr19:47189184 | A | G | 2 | a0001c0001t0001g0301 a0001c0001t0001g0341 |
2 | HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.734-8049A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189184 | |||||||
| chr19:47189311 | G | A | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.734-7922G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189311 | |||||||
| chr19:47189443 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.734-7790C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189443 | |||||||
| chr19:47189492 | C | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0215 |
3 | HG02055.hp2 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.734-7741C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189492 | |||||||
| chr19:47189613 | C | T | 45 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(42): Show |
45 | HG00733.hp2 HG01069.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.734-7620C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189613 | |||||||
| chr19:47189677 | G | C | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-7556G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189677 | |||||||
| chr19:47189725 | A | C | 1 | a0001c0001t0001g0191 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.734-7508A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189725 | |||||||
| chr19:47189794 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-7439C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189794 | |||||||
| chr19:47189839 | A | C | 1 | a0001c0001t0001g0093 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.734-7394A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189839 | |||||||
| chr19:47189904 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(85): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.734-7329C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47189904 | |||||||
| chr19:47190345 | ATG | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(82): Show |
85 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.734-6883_734-6882d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47190345 | ||||||
| chr19:47190440 | G | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.734-6793G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47190440 | |||||||
| chr19:47190473 | GC | G | 6 | a0002c0002t0001g0039 a0002c0002t0001g0062 a0002c0002t0001g0063 others(3): Show |
6 | NA18942.hp2 NA18945.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-6754delC | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47190473 | ||||||
| chr19:47190573 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.734-6660G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47190573 | |||||||
| chr19:47190714 | C | T | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.734-6519C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47190714 | |||||||
| chr19:47190977 | C | G | 2 | a0001c0001t0001g0351 a0001c0001t0001g0353 |
2 | HG00597.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.734-6256C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47190977 | |||||||
| chr19:47190995 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.734-6238A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47190995 | |||||||
| chr19:47191154 | T | C | 6 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-6079T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191154 | |||||||
| chr19:47191204 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.734-6029A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191204 | |||||||
| chr19:47191243 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.734-5990A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191243 | |||||||
| chr19:47191284 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.734-5949G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191284 | |||||||
| chr19:47191294 | T | C | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.734-5939T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191294 | |||||||
| chr19:47191615 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.734-5618G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191615 | |||||||
| chr19:47191665 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0093 others(85): Show |
88 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.734-5568A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191665 | |||||||
| chr19:47191780 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-5453G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191780 | |||||||
| chr19:47191783 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-5450C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191783 | |||||||
| chr19:47191823 | A | G | 15 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0097 others(12): Show |
15 | HG01109.hp1 HG01515.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.734-5410A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191823 | |||||||
| chr19:47191974 | A | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0224 a0001c0001t0001g0225 others(44): Show |
47 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.734-5259A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191974 | |||||||
| chr19:47191977 | C | G | 42 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(39): Show |
42 | HG01070.hp2 HG01074.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.734-5256C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47191977 | |||||||
| chr19:47192011 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02647.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.734-5222G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192011 | |||||||
| chr19:47192053 | C | CA | 10 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.734-5167dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47192053 | ||||||
| chr19:47192187 | T | A | 1 | a0001c0001t0001g0319 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.734-5046T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192187 | |||||||
| chr19:47192205 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734-5028C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192205 | |||||||
| chr19:47192258 | G | A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-4975G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192258 | |||||||
| chr19:47192319 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.734-4914C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192319 | |||||||
| chr19:47192353 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.734-4880C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192353 | |||||||
| chr19:47192493 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.734-4740C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192493 | |||||||
| chr19:47192494 | G | T | 99 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
99 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.734-4739G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192494 | |||||||
| chr19:47192532 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.734-4701C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47192532 | |||||||
| chr19:47193057 | C | CT | 35 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(32): Show |
35 | HG00408.hp2 HG01109.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.734-4159dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47193057 | ||||||
| chr19:47193057 | CT | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0048 others(5): Show |
8 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-4159delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47193057 | ||||||
| chr19:47193079 | A | G | 108 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
108 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.734-4154A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47193079 | |||||||
| chr19:47193219 | G | A | 8 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG01123.hp1 HG01928.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.734-4014G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47193219 | |||||||
| chr19:47193258 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.734-3975G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47193258 | |||||||
| chr19:47193369 | C | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(337): Show |
340 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(337): Show |
intron_variant | MODIFIER | c.734-3864C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47193369 | |||||||
| chr19:47193836 | AAAAAGAA others(2): Show |
A | 8 | a0001c0001t0001g0296 a0001c0001t0001g0300 a0001c0001t0001g0303 others(5): Show |
8 | NA18963.hp2 NA18965.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-3388_734-3380d others(11): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47193836 | ||||||
| chr19:47193841 | GAAAGA | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0092 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.734-3383_734-3379d others(7): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47193841 | ||||||
| chr19:47193845 | GAAAAGA | G | 23 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0001g0203 others(20): Show |
23 | HG00733.hp2 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.734-3373_734-3368d others(8): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47193845 | ||||||
| chr19:47194049 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.734-3184C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194049 | |||||||
| chr19:47194319 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.734-2914T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194319 | |||||||
| chr19:47194351 | T | C | 1 | a0001c0001t0001g0337 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-2882T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194351 | |||||||
| chr19:47194452 | A | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG02056.hp1 NA19011.hp2 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-2781A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194452 | |||||||
| chr19:47194544 | G | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0234 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.734-2689G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194544 | |||||||
| chr19:47194606 | T | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG02818.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.734-2627T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194606 | |||||||
| chr19:47194611 | AGAGACAA others(5): Show |
A | 1 | a0001c0001t0001g0298 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.734-2616_734-2605d others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47194611 | ||||||
| chr19:47194656 | G | A | 1 | a0005c0008t0006g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.734-2577G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194656 | |||||||
| chr19:47194683 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-2550G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194683 | |||||||
| chr19:47194747 | C | CT | 38 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0074 others(35): Show |
38 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.734-2466dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47194747 | ||||||
| chr19:47194747 | CT | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0093 a0001c0001t0001g0158 others(8): Show |
11 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.734-2466delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47194747 | ||||||
| chr19:47194747 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0298 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.734-2476_734-2466d others(13): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47194747 | ||||||
| chr19:47194748 | T | G | 1 | a0007c0009t0001g0241 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.734-2485T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194748 | |||||||
| chr19:47194765 | T | C | 4 | a0001c0001t0002g0091 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG02886.hp2 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2468T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194765 | |||||||
| chr19:47194935 | G | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.734-2298G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194935 | |||||||
| chr19:47194946 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0234 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.734-2287T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194946 | |||||||
| chr19:47194994 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.734-2239C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47194994 | |||||||
| chr19:47195022 | C | T | 5 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0242 others(2): Show |
5 | HG00642.hp2 HG01168.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-2211C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47195022 | |||||||
| chr19:47195055 | C | CT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0247 a0001c0001t0001g0280 others(4): Show |
7 | HG02809.hp2 HG03579.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-2163dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47195055 | ||||||
| chr19:47195659 | C | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.734-1574C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47195659 | |||||||
| chr19:47195682 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.734-1551C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47195682 | |||||||
| chr19:47195705 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.734-1528C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47195705 | |||||||
| chr19:47195736 | C | CT | 6 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0116 others(3): Show |
6 | HG01169.hp1 HG03139.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-1478dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47195736 | ||||||
| chr19:47195736 | CT | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(262): Show |
265 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(262): Show |
intron_variant | MODIFIER | c.734-1478delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47195736 | ||||||
| chr19:47195736 | CTT | C | 47 | a0001c0001t0001g0042 a0001c0001t0001g0055 a0001c0001t0001g0099 others(44): Show |
47 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.734-1479_734-1478d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47195736 | ||||||
| chr19:47195889 | T | C | 375 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(372): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.734-1344T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47195889 | |||||||
| chr19:47195897 | A | AT | 15 | a0001c0001t0001g0015 a0001c0001t0001g0150 a0001c0001t0001g0209 others(12): Show |
15 | HG00438.hp1 HG02132.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.734-1320dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47195897 | ||||||
| chr19:47196041 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.734-1192G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196041 | |||||||
| chr19:47196044 | C | CT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0001g0257 others(5): Show |
8 | HG00597.hp1 HG02809.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-1172dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196044 | ||||||
| chr19:47196044 | CT | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0137 a0001c0001t0003g0003 others(3): Show |
6 | HG02280.hp2 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-1172delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196044 | ||||||
| chr19:47196046 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.734-1187T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196046 | |||||||
| chr19:47196069 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0234 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.734-1164G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196069 | |||||||
| chr19:47196333 | C | CT | 18 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
18 | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.734-866dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196333 | C | CTT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0101 a0001c0001t0001g0121 others(3): Show |
6 | HG00735.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-867_734-866dup others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196333 | C | CTTT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0100 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-868_734-866dup others(3): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196333 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.734-900C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196333 | |||||||
| chr19:47196333 | CTT | C | 11 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0001g0207 others(8): Show |
11 | HG02572.hp1 HG02717.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.734-867_734-866del others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196333 | CTTT | C | 45 | a0001c0001t0001g0023 a0001c0001t0001g0093 a0001c0001t0001g0096 others(42): Show |
45 | HG00597.hp1 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.734-868_734-866del others(3): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196333 | CTTTT | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
112 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.734-869_734-866del others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196333 | CTTTTT | C | 86 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
86 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.734-870_734-866del others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196333 | CTTTTTT | C | 68 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0037 others(65): Show |
68 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.734-871_734-866del others(6): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196333 | CTTTTTTT | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0087 a0001c0001t0001g0226 others(6): Show |
9 | HG01169.hp2 HG01978.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-872_734-866del others(7): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 47196333 | ||||||
| chr19:47196367 | T | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0223 |
3 | HG02572.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.734-866T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196367 | |||||||
| chr19:47196370 | T | A | 1 | a0007c0009t0001g0241 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.734-863T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196370 | |||||||
| chr19:47196450 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(214): Show |
217 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.734-783G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196450 | |||||||
| chr19:47196564 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0207 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.734-669A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196564 | |||||||
| chr19:47196617 | C | G | 19 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(16): Show |
19 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.734-616C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196617 | |||||||
| chr19:47196633 | G | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.734-600G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196633 | |||||||
| chr19:47196675 | A | G | 9 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(6): Show |
9 | HG02132.hp2 HG02602.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-558A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196675 | |||||||
| chr19:47196848 | A | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0092 others(86): Show |
89 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.734-385A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196848 | |||||||
| chr19:47196948 | C | G | 1 | a0001c0001t0001g0327 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.734-285C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47196948 | |||||||
| chr19:47197047 | G | T | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.734-186G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 6/8 | chr19 | 47197047 | |||||||
| chr19:47197420 | GT | G | 42 | a0001c0001t0001g0023 a0001c0001t0001g0092 a0001c0001t0001g0093 others(39): Show |
42 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.878+46delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47197420 | ||||||
| chr19:47197450 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878+73A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47197450 | |||||||
| chr19:47197603 | A | G | 20 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 others(17): Show |
20 | HG00733.hp2 HG01243.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.878+226A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47197603 | |||||||
| chr19:47197612 | G | A | 1 | a0001c0001t0002g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.878+235G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47197612 | |||||||
| chr19:47197730 | T | C | 1 | a0001c0001t0001g0360 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.878+353T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47197730 | |||||||
| chr19:47197922 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.878+545C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47197922 | |||||||
| chr19:47198131 | CAG | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
8 | NA18945.hp2 NA18952.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.878+757_878+758del others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47198131 | ||||||
| chr19:47198143 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878+766C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198143 | |||||||
| chr19:47198187 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.878+810G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198187 | |||||||
| chr19:47198355 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.878+978G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198355 | |||||||
| chr19:47198364 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.878+987G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198364 | |||||||
| chr19:47198403 | C | T | 5 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(2): Show |
5 | HG02647.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.878+1026C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198403 | |||||||
| chr19:47198554 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878+1177G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198554 | |||||||
| chr19:47198584 | C | A | 2 | a0001c0001t0001g0096 a0001c0001t0007g0148 |
2 | HG00544.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.878+1207C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198584 | |||||||
| chr19:47198615 | A | G | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878+1238A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198615 | |||||||
| chr19:47198686 | C | T | 6 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01261.hp1 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.878+1309C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198686 | |||||||
| chr19:47198744 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.878+1367T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198744 | |||||||
| chr19:47198904 | T | C | 1 | a0002c0002t0001g0045 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.878+1527T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198904 | |||||||
| chr19:47198920 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.878+1543C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198920 | |||||||
| chr19:47198998 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18942.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.878+1621G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47198998 | |||||||
| chr19:47199390 | C | CA | 67 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(64): Show |
67 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.878+2036dupA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47199390 | ||||||
| chr19:47199390 | C | CAA | 6 | a0001c0001t0001g0036 a0001c0001t0001g0228 a0001c0001t0001g0276 others(3): Show |
6 | HG02132.hp2 HG02735.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.878+2035_878+2036d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47199390 | ||||||
| chr19:47199390 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(91): Show |
94 | HG00099.hp1 HG00738.hp1 HG01168.hp1 others(91): Show |
intron_variant | MODIFIER | c.878+2036delA | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47199390 | ||||||
| chr19:47199415 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG00738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.878+2038G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47199415 | |||||||
| chr19:47199578 | T | C | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.878+2201T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47199578 | |||||||
| chr19:47199658 | A | C | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.878+2281A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47199658 | |||||||
| chr19:47199865 | A | G | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG02132.hp2 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.878+2488A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47199865 | |||||||
| chr19:47199884 | CTGA | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0149 a0001c0001t0001g0286 |
3 | NA18946.hp1 NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.878+2510_878+2512d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47199884 | ||||||
| chr19:47199934 | C | CT | 14 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0061 others(11): Show |
14 | HG01361.hp2 HG01515.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.878+2570dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47199934 | ||||||
| chr19:47200080 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0051 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.878+2703G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47200080 | |||||||
| chr19:47200096 | AATTTTTT others(4): Show |
A | 7 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(4): Show |
7 | HG00621.hp1 NA18949.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.878+2727_878+2737d others(13): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47200096 | ||||||
| chr19:47200146 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.878+2769G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47200146 | |||||||
| chr19:47200224 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0158 |
2 | HG00558.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.878+2847C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47200224 | |||||||
| chr19:47200234 | CT | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0001t0001g0206 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.878+2874delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47200234 | ||||||
| chr19:47200399 | A | AT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0021 others(36): Show |
39 | HG00733.hp2 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.878+3046dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47200399 | ||||||
| chr19:47200399 | AT | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.878+3046delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47200399 | ||||||
| chr19:47200399 | ATT | A | 39 | a0001c0001t0001g0047 a0001c0001t0001g0092 a0001c0001t0001g0232 others(36): Show |
39 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.878+3045_878+3046d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47200399 | ||||||
| chr19:47200399 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.878+3036_878+3046d others(13): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47200399 | ||||||
| chr19:47200561 | C | T | 107 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(104): Show |
107 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.879-3110C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47200561 | |||||||
| chr19:47200858 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879-2813G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47200858 | |||||||
| chr19:47200919 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(107): Show |
110 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.879-2752A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47200919 | |||||||
| chr19:47200957 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.879-2714A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47200957 | |||||||
| chr19:47200985 | G | A | 7 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0106 others(4): Show |
7 | HG01261.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.879-2686G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47200985 | |||||||
| chr19:47201260 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.879-2411A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47201260 | |||||||
| chr19:47201264 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.879-2407A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47201264 | |||||||
| chr19:47201360 | C | CT | 49 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0036 others(46): Show |
49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.879-2282dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTT | 50 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0040 others(47): Show |
50 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.879-2283_879-2282d others(4): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTT | 30 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0028 others(27): Show |
30 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.879-2284_879-2282d others(5): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTT | 22 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0048 others(19): Show |
22 | HG00621.hp2 HG00642.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.879-2285_879-2282d others(6): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTT | 21 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0027 others(18): Show |
21 | HG00408.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.879-2286_879-2282d others(7): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTT | 15 | a0001c0001t0001g0035 a0001c0001t0001g0122 a0001c0001t0001g0149 others(12): Show |
15 | HG01123.hp1 HG01243.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.879-2287_879-2282d others(8): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0123 others(3): Show |
6 | HG01361.hp1 HG01934.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.879-2289_879-2282d others(10): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0052 others(7): Show |
10 | HG01074.hp1 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.879-2290_879-2282d others(11): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0001g0276 |
3 | HG02132.hp2 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.879-2291_879-2282d others(12): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.879-2293_879-2282d others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0211 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.879-2294_879-2282d others(15): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.879-2296_879-2282d others(17): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879-2304_879-2282d others(25): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.879-2307_879-2282d others(28): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0279 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.879-2282_879-2281i others(32): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | CT | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0132 others(5): Show |
8 | HG01257.hp1 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.879-2282delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0092 a0001c0001t0001g0234 others(5): Show |
8 | HG01433.hp2 HG02738.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.879-2289_879-2282d others(10): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | CTTTTTTT others(2): Show |
C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0099 others(79): Show |
82 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.879-2290_879-2282d others(11): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0240 a0001c0001t0001g0256 |
3 | HG01943.hp2 NA18939.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.879-2291_879-2282d others(12): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | CTTTTTTT others(4): Show |
C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0217 a0001c0001t0001g0218 others(5): Show |
8 | HG00733.hp2 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.879-2292_879-2282d others(13): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0001g0087 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG02280.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.879-2293_879-2282d others(14): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0003g0032 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.879-2294_879-2282d others(15): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201360 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.879-2295_879-2282d others(16): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201360 | ||||||
| chr19:47201465 | A | G | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.879-2206A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47201465 | |||||||
| chr19:47201481 | TTTGCCTC others(6): Show |
T | 1 | a0007c0009t0001g0241 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.879-2188_879-2176d others(15): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 47201481 | ||||||
| chr19:47201693 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.879-1978G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47201693 | |||||||
| chr19:47201883 | T | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0333 |
2 | HG02602.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.879-1788T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47201883 | |||||||
| chr19:47202026 | G | A | 111 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
111 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.879-1645G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202026 | |||||||
| chr19:47202169 | G | A | 6 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG02647.hp2 HG03139.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.879-1502G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202169 | |||||||
| chr19:47202296 | T | A | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG02132.hp2 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.879-1375T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202296 | |||||||
| chr19:47202407 | C | T | 1 | a0001c0001t0001g0378 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.879-1264C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202407 | |||||||
| chr19:47202416 | T | C | 1 | a0001c0001t0001g0365 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.879-1255T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202416 | |||||||
| chr19:47202427 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.879-1244A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202427 | |||||||
| chr19:47202495 | C | T | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.879-1176C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202495 | |||||||
| chr19:47202510 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.879-1161T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202510 | |||||||
| chr19:47202529 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG00408.hp2 HG01261.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.879-1142G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202529 | |||||||
| chr19:47202538 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0185 |
2 | HG01358.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.879-1133G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202538 | |||||||
| chr19:47202570 | G | T | 1 | a0001c0001t0001g0284 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.879-1101G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202570 | |||||||
| chr19:47202586 | T | C | 3 | a0001c0001t0001g0356 a0001c0001t0001g0361 a0001c0001t0001g0362 |
3 | NA18954.hp2 NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.879-1085T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202586 | |||||||
| chr19:47202684 | C | T | 1 | a0004c0010t0001g0293 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.879-987C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202684 | |||||||
| chr19:47202689 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.879-982G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202689 | |||||||
| chr19:47202766 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.879-905C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202766 | |||||||
| chr19:47202778 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | NA18941.hp2 NA18947.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.879-893C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202778 | |||||||
| chr19:47202863 | T | C | 2 | a0001c0001t0001g0310 a0001c0001t0001g0320 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.879-808T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47202863 | |||||||
| chr19:47203266 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.879-405C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47203266 | |||||||
| chr19:47203428 | A | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG03017.hp1 HG03704.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.879-243A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47203428 | |||||||
| chr19:47203429 | A | C | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG02132.hp2 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.879-242A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47203429 | |||||||
| chr19:47203482 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.879-189A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47203482 | |||||||
| chr19:47203554 | G | A | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.879-117G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47203554 | |||||||
| chr19:47203602 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.879-69A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47203602 | |||||||
| chr19:47203617 | A | G | 2 | a0001c0001t0004g0098 a0001c0001t0004g0273 |
2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.879-54A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47203617 | |||||||
| chr19:47203623 | A | C | 1 | a0002c0002t0001g0070 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.879-48A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 7/8 | chr19 | 47203623 | |||||||
| chr19:47203901 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0109 |
2 | HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.948+161C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47203901 | |||||||
| chr19:47204140 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.948+400C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204140 | |||||||
| chr19:47204170 | T | G | 102 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(99): Show |
102 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.948+430T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204170 | |||||||
| chr19:47204187 | C | CT | 31 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(28): Show |
31 | HG00597.hp1 HG01257.hp2 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.948+475dupT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47204187 | ||||||
| chr19:47204187 | C | CTT | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(9): Show |
12 | HG01069.hp1 HG01257.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.948+474_948+475dup others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47204187 | ||||||
| chr19:47204187 | C | CTTT | 7 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0020 others(4): Show |
7 | NA18939.hp2 NA18972.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.948+473_948+475dup others(3): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47204187 | ||||||
| chr19:47204187 | CT | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(177): Show |
180 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.948+475delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47204187 | ||||||
| chr19:47204187 | CTT | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0037 others(12): Show |
15 | HG00642.hp1 HG01074.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.948+474_948+475del others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47204187 | ||||||
| chr19:47204236 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.948+496C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204236 | |||||||
| chr19:47204256 | A | G | 2 | a0001c0001t0008g0231 a0001c0011t0001g0343 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.948+516A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204256 | |||||||
| chr19:47204316 | G | A | 6 | a0002c0002t0001g0039 a0002c0002t0001g0062 a0002c0002t0001g0063 others(3): Show |
6 | NA18942.hp2 NA18945.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.948+576G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204316 | |||||||
| chr19:47204348 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.948+608C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204348 | |||||||
| chr19:47204434 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.948+694G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204434 | |||||||
| chr19:47204437 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.948+697A>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204437 | |||||||
| chr19:47204489 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.948+749T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204489 | |||||||
| chr19:47204500 | A | AC | 170 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(167): Show |
170 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.948+769dupC | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47204500 | ||||||
| chr19:47204500 | A | ACC | 40 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0051 others(37): Show |
40 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.948+768_948+769dup others(2): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47204500 | ||||||
| chr19:47204509 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.948+769C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204509 | |||||||
| chr19:47204510 | T | C | 17 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0071 others(14): Show |
17 | HG01070.hp2 HG01109.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.948+770T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204510 | |||||||
| chr19:47204658 | C | A | 1 | a0001c0001t0001g0309 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.948+918C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204658 | |||||||
| chr19:47204659 | A | C | 1 | a0001c0001t0001g0309 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.948+919A>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204659 | |||||||
| chr19:47204663 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0093 a0001c0001t0001g0235 others(1): Show |
4 | NA18971.hp1 NA18992.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.948+923C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204663 | |||||||
| chr19:47204765 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.948+1025G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47204765 | |||||||
| chr19:47205034 | C | A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.948+1294C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205034 | |||||||
| chr19:47205077 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.948+1337C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205077 | |||||||
| chr19:47205320 | CT | C | 275 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(272): Show |
275 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.948+1597delT | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47205320 | ||||||
| chr19:47205564 | G | A | 11 | a0001c0001t0002g0006 a0001c0001t0002g0091 a0001c0001t0002g0094 others(8): Show |
11 | HG02280.hp2 HG02723.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.948+1824G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205564 | |||||||
| chr19:47205589 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0320 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.948+1849G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205589 | |||||||
| chr19:47205636 | AATGGGAA others(7): Show |
A | 1 | a0001c0001t0001g0372 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.948+1899_948+1912d others(16): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47205636 | ||||||
| chr19:47205638 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.948+1898T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205638 | |||||||
| chr19:47205722 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.948+1982C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205722 | |||||||
| chr19:47205816 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.948+2076T>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205816 | |||||||
| chr19:47205912 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.948+2172C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205912 | |||||||
| chr19:47205992 | C | G | 1 | a0001c0001t0001g0246 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.948+2252C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47205992 | |||||||
| chr19:47206046 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.948+2306A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47206046 | |||||||
| chr19:47206376 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.948+2636A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47206376 | |||||||
| chr19:47206526 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.949-2633T>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47206526 | |||||||
| chr19:47206660 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.949-2499C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47206660 | |||||||
| chr19:47206680 | G | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.949-2479G>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47206680 | |||||||
| chr19:47206721 | C | G | 1 | a0001c0003t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.949-2438C>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47206721 | |||||||
| chr19:47206797 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0084 |
2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.949-2362C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47206797 | |||||||
| chr19:47206987 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0320 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.949-2172G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47206987 | |||||||
| chr19:47207029 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.949-2130C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207029 | |||||||
| chr19:47207190 | G | A | 43 | a0001c0001t0001g0023 a0001c0001t0001g0092 a0001c0001t0001g0093 others(40): Show |
43 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.949-1969G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207190 | |||||||
| chr19:47207220 | C | A | 1 | a0001c0001t0008g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.949-1939C>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207220 | |||||||
| chr19:47207414 | G | A | 4 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0032 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.949-1745G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207414 | |||||||
| chr19:47207479 | TG | T | 42 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0232 others(39): Show |
42 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.949-1678delG | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47207479 | ||||||
| chr19:47207753 | G | C | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.949-1406G>C | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207753 | |||||||
| chr19:47207823 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.949-1336A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207823 | |||||||
| chr19:47207864 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.949-1295G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207864 | |||||||
| chr19:47207912 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.949-1247A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207912 | |||||||
| chr19:47207994 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.949-1165A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47207994 | |||||||
| chr19:47208200 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.949-959T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47208200 | |||||||
| chr19:47208336 | T | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0223 |
3 | HG02572.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.949-823T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47208336 | |||||||
| chr19:47208496 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.949-663G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47208496 | |||||||
| chr19:47208545 | A | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(56): Show |
59 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.949-614A>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47208545 | |||||||
| chr19:47208566 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.949-593G>A | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47208566 | |||||||
| chr19:47208597 | TGTATTTT others(11): Show |
T | 1 | a0001c0001t0001g0242 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.949-560_949-543del others(18): Show |
SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 47208597 | ||||||
| chr19:47208674 | T | G | 1 | a0001c0001t0001g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.949-485T>G | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47208674 | |||||||
| chr19:47208745 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.949-414C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47208745 | |||||||
| chr19:47208782 | C | T | 1 | a0001c0011t0001g0343 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.949-377C>T | SAE1 | ENSG00000142230.13 | transcript | ENST00000270225.12 | protein_coding | 8/8 | chr19 | 47208782 |