Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10626 |
| ensemblid | ENSG00000221926.13 |
| hgncid | 17241 |
| symbol | TRIM16 |
| name | tripartite motif containing 16 |
| refseq_nuc | NM_001348119.1 |
| refseq_prot | NP_001335048.1 |
| ensembl_nuc | ENST00000649191.2 |
| ensembl_prot | ENSP00000497185.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 15627966 |
| end | 15684311 |
| strand | - |
| ver | v1.2 |
| region | chr17:15627966-15684311 |
| region5000 | chr17:15622966-15689311 |
| regionname0 | TRIM16_chr17_15627966_15684311 |
| regionname5000 | TRIM16_chr17_15622966_15689311 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 564 | 186 | 37 | 46 | 86 | 2 | 13 | 66 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0002 | 0/0 | 564 | 106 | 21 | 17 | 52 | 3 | 13 | 34 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0003 | 0/0 | 564 | 28 | 26 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0004 | 0/0 | 564 | 20 | 0 | 1 | 14 | 0 | 5 | 11 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0005 | 0/0 | 564 | 5 | 4 | 0 | 0 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0006 | 0/0 | 564 | 5 | 1 | 2 | 2 | 0 | 0 | 2 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0007 | 0/0 | 564 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0008 | 0/0 | 47 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(42): Show |
chr17 | 15622966 | 15689311 |
| a0009 | 0/0 | 564 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0010 | 0/0 | 564 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0011 | 0/0 | 564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| a0012 | 0/0 | 564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | MAELD others(559): Show |
chr17 | 15622966 | 15689311 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1692 | 170 | 26 | 43 | 84 | 2 | 13 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0001c0007 | 0/0 | 1692 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0001c0010 | 0/0 | 1692 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0001c0011 | 0/0 | 1692 | 4 | 0 | 2 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0001c0024 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0002c0002 | 0/0 | 1692 | 86 | 18 | 14 | 42 | 3 | 9 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0002c0005 | 0/0 | 1692 | 10 | 0 | 0 | 9 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0002c0006 | 0/0 | 1692 | 9 | 3 | 3 | 1 | 0 | 2 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0002c0026 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0003c0004 | 0/0 | 1692 | 14 | 14 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0003c0008 | 0/0 | 1692 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0003c0014 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0003c0015 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0003c0017 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0003c0025 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0004c0003 | 0/0 | 1692 | 20 | 0 | 1 | 14 | 0 | 5 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0005c0012 | 0/0 | 1692 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0005c0021 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0006c0009 | 0/0 | 1692 | 5 | 1 | 2 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0007c0013 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0008c0018 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0008c0019 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0009c0016 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0010c0023 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0011c0020 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 | ||
| a0012c0022 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | ATGGC others(1687): Show |
chr17 | 15622966 | 15689311 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3358 | 119 | 15 | 36 | 58 | 1 | 7 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0002 | 0/0 | 3358 | 34 | 3 | 2 | 24 | 0 | 5 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0004 | 0/0 | 3359 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0005 | 0/0 | 3359 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0006 | 0/0 | 3358 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0007 | 0/0 | 3358 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0010 | 0/0 | 3358 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0013 | 0/0 | 3358 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0018 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0019 | 0/0 | 3359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0001c0001t0025 | 0/0 | 3358 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0007t0001 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0007t0002 | 0/0 | 3358 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0007t0007 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0007t0012 | 0/0 | 3358 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GCTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0010t0006 | 0/0 | 3358 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0011t0001 | 0/0 | 3358 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0011t0014 | 0/0 | 3358 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0001c0024t0007 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0002t0001 | 0/0 | 3358 | 15 | 7 | 0 | 6 | 0 | 2 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0002t0002 | 0/0 | 3358 | 65 | 7 | 13 | 36 | 3 | 6 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0002t0004 | 0/0 | 3359 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0002c0002t0007 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0002t0009 | 0/0 | 3358 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0002t0021 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0002t0022 | 0/0 | 3358 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0005t0001 | 0/0 | 3358 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0005t0002 | 0/0 | 3358 | 8 | 0 | 0 | 7 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0006t0001 | 0/0 | 3358 | 9 | 3 | 3 | 1 | 0 | 2 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0002c0026t0002 | 0/0 | 3358 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0003c0004t0003 | 0/0 | 3358 | 13 | 13 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0003c0004t0024 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0003c0008t0008 | 0/0 | 3359 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0003c0014t0005 | 0/0 | 3359 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0003c0014t0008 | 0/0 | 3359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0003c0014t0015 | 0/0 | 3359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0003c0015t0001 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0003c0015t0004 | 0/0 | 3359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0003c0015t0005 | 0/0 | 3359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0003c0017t0003 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0003c0017t0017 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0003c0025t0004 | 0/0 | 3359 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0004c0003t0001 | 0/0 | 3358 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0004c0003t0004 | 0/0 | 3359 | 12 | 0 | 0 | 7 | 0 | 5 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0004c0003t0005 | 0/0 | 3359 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0004c0003t0011 | 0/0 | 3359 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0004c0003t0026 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0005c0012t0016 | 0/0 | 3359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0005c0012t0020 | 0/0 | 3359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0005c0012t0027 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0005c0012t0028 | 0/0 | 3359 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3354): Show |
chr17 | 15622966 | 15689311 |
| a0005c0021t0002 | 0/0 | 3358 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0006c0009t0001 | 0/0 | 3358 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0006c0009t0002 | 0/0 | 3358 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0007c0013t0001 | 0/0 | 3358 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0007c0013t0009 | 0/0 | 3358 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0008c0018t0002 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0008c0019t0002 | 0/0 | 3358 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0009c0016t0003 | 0/0 | 3358 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0010c0023t0001 | 0/0 | 3358 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0011c0020t0001 | 0/0 | 3358 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| a0012c0022t0023 | 0/0 | 3358 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | GTTTC others(3353): Show |
chr17 | 15622966 | 15689311 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0003 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0010g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0010g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0013g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0013g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0018g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0019g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0001t0025g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0007t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0007t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0007t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0007t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0007t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0007t0012g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0010t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0010t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0010t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0010t0006g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0011t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0011t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0011t0014g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0011t0014g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0001c0024t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0021g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0002t0022g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0005t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0006t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0002c0026t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0004t0024g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0008t0008g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0008t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0014t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0014t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0014t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0015t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0015t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0015t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0017t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0017t0017g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0003c0025t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0011g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0011g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0004c0003t0026g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0005c0012t0016g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0005c0012t0020g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0005c0012t0027g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0005c0012t0028g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0005c0021t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0006c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0006c0009t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0006c0009t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0006c0009t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0006c0009t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0007c0013t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0007c0013t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0008c0018t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0008c0019t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0009c0016t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0009c0016t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0010c0023t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0011c0020t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| a0012c0022t0023g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0016 | EUR | FIN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00323 | hp2 | a0010 | c0023 | t0001 | g0054 | EUR | FIN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00408 | hp2 | a0002 | c0005 | t0002 | g0225 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0308 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00597 | hp2 | a0008 | c0018 | t0002 | g0311 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0321 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00621 | hp2 | a0004 | c0003 | t0004 | g0319 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0244 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00642 | hp2 | a0011 | c0020 | t0001 | g0114 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | CHS | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0216 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00738 | hp2 | a0003 | c0014 | t0005 | g0112 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG00741 | hp2 | a0002 | c0002 | t0022 | g0278 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01070 | hp2 | a0004 | c0003 | t0001 | g0104 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0215 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01168 | hp2 | a0002 | c0006 | t0001 | g0180 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0224 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01192 | hp2 | a0002 | c0006 | t0001 | g0096 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01243 | hp1 | a0002 | c0006 | t0001 | g0082 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0217 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01255 | hp2 | a0001 | c0001 | t0010 | g0197 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0274 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01257 | hp1 | a0001 | c0001 | t0013 | g0196 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01258 | hp2 | a0001 | c0001 | t0013 | g0195 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01261 | hp2 | a0001 | c0011 | t0001 | g0094 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01346 | hp2 | a0003 | c0025 | t0004 | g0313 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01433 | hp1 | a0001 | c0011 | t0001 | g0101 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0238 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01884 | hp1 | a0003 | c0008 | t0008 | g0001 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01884 | hp2 | a0005 | c0012 | t0027 | g0328 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0193 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01891 | hp2 | a0001 | c0001 | t0018 | g0090 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0220 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01934 | hp2 | a0001 | c0010 | t0006 | g0331 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0013 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01952 | hp2 | a0006 | c0009 | t0002 | g0213 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0267 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0237 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01981 | hp2 | a0012 | c0022 | t0023 | g0223 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG01993 | hp2 | a0006 | c0009 | t0002 | g0214 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02055 | hp1 | a0001 | c0007 | t0002 | g0254 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0194 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02080 | hp2 | a0004 | c0003 | t0004 | g0303 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0291 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02145 | hp1 | a0005 | c0012 | t0016 | g0023 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02145 | hp2 | a0003 | c0004 | t0003 | g0169 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | CDX | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CDX | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | CDX | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02257 | hp1 | a0006 | c0009 | t0002 | g0295 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02257 | hp2 | a0007 | c0013 | t0001 | g0009 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02258 | hp1 | a0003 | c0004 | t0003 | g0011 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02258 | hp2 | a0001 | c0007 | t0002 | g0258 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02280 | hp1 | a0007 | c0013 | t0009 | g0025 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0239 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0268 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0219 | AMR | PEL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02451 | hp1 | a0001 | c0024 | t0007 | g0190 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0261 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02523 | hp1 | a0004 | c0003 | t0004 | g0296 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0255 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02572 | hp2 | a0005 | c0012 | t0028 | g0329 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02615 | hp2 | a0001 | c0001 | t0019 | g0123 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02622 | hp2 | a0003 | c0014 | t0008 | g0186 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02630 | hp1 | a0002 | c0002 | t0009 | g0022 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02630 | hp2 | a0002 | c0006 | t0001 | g0097 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02647 | hp2 | a0003 | c0004 | t0003 | g0079 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02683 | hp1 | a0004 | c0003 | t0004 | g0298 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02698 | hp1 | a0002 | c0006 | t0001 | g0179 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0230 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02717 | hp1 | a0002 | c0002 | t0021 | g0189 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0324 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02723 | hp1 | a0003 | c0015 | t0004 | g0259 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02735 | hp1 | a0005 | c0021 | t0002 | g0253 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0325 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02818 | hp2 | a0009 | c0016 | t0003 | g0128 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02886 | hp1 | a0001 | c0007 | t0001 | g0089 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02886 | hp2 | a0001 | c0007 | t0012 | g0006 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02895 | hp1 | a0005 | c0012 | t0020 | g0077 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02896 | hp2 | a0003 | c0004 | t0003 | g0072 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02897 | hp1 | a0003 | c0004 | t0003 | g0073 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02922 | hp1 | a0001 | c0007 | t0007 | g0187 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02970 | hp1 | a0003 | c0004 | t0003 | g0078 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02970 | hp2 | a0003 | c0017 | t0017 | g0027 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02976 | hp1 | a0007 | c0013 | t0001 | g0009 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02976 | hp2 | a0002 | c0002 | t0009 | g0026 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0234 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03041 | hp1 | a0003 | c0017 | t0003 | g0116 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03041 | hp2 | a0002 | c0006 | t0001 | g0099 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03098 | hp1 | a0003 | c0004 | t0024 | g0257 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03130 | hp1 | a0003 | c0004 | t0003 | g0168 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03130 | hp2 | a0003 | c0004 | t0003 | g0075 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03195 | hp1 | a0003 | c0004 | t0003 | g0011 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03225 | hp1 | a0003 | c0015 | t0001 | g0105 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0245 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0231 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03453 | hp2 | a0001 | c0010 | t0006 | g0326 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03486 | hp1 | a0001 | c0010 | t0006 | g0323 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03491 | hp1 | a0002 | c0006 | t0001 | g0175 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0304 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0327 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03540 | hp2 | a0002 | c0002 | t0007 | g0191 | AFR | GWD | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03579 | hp1 | a0003 | c0004 | t0003 | g0182 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0263 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03654 | hp2 | a0002 | c0026 | t0002 | g0265 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03669 | hp1 | a0004 | c0003 | t0004 | g0310 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | BEB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03831 | hp2 | a0004 | c0003 | t0004 | g0297 | SAS | BEB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03942 | hp1 | a0001 | c0001 | t0025 | g0249 | SAS | BEB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04115 | hp2 | a0004 | c0003 | t0004 | g0229 | SAS | STU | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0266 | SAS | BEB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04184 | hp2 | a0002 | c0005 | t0002 | g0207 | SAS | BEB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | STU | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | STU | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04204 | hp2 | a0004 | c0003 | t0004 | g0306 | SAS | STU | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04228 | hp1 | a0002 | c0002 | t0004 | g0250 | SAS | STU | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18522 | hp1 | a0009 | c0016 | t0003 | g0126 | AFR | YRI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18522 | hp2 | a0003 | c0008 | t0008 | g0001 | AFR | YRI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | CHB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0212 | AFR | YRI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0119 | AFR | YRI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18940 | hp1 | a0002 | c0005 | t0002 | g0210 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18941 | hp1 | a0002 | c0005 | t0002 | g0309 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18943 | hp2 | a0004 | c0003 | t0005 | g0108 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18948 | hp2 | a0004 | c0003 | t0004 | g0020 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18954 | hp2 | a0001 | c0011 | t0014 | g0333 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18960 | hp1 | a0004 | c0003 | t0011 | g0299 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18970 | hp2 | a0006 | c0009 | t0001 | g0106 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18975 | hp1 | a0004 | c0003 | t0004 | g0322 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18979 | hp2 | a0002 | c0006 | t0001 | g0141 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18983 | hp1 | a0006 | c0009 | t0001 | g0115 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18984 | hp1 | a0004 | c0003 | t0005 | g0110 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18989 | hp2 | a0004 | c0003 | t0026 | g0302 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18990 | hp1 | a0004 | c0003 | t0004 | g0202 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18992 | hp2 | a0002 | c0005 | t0002 | g0208 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18997 | hp2 | a0002 | c0005 | t0002 | g0292 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18999 | hp1 | a0002 | c0005 | t0001 | g0039 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19003 | hp2 | a0002 | c0005 | t0001 | g0068 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19007 | hp2 | a0004 | c0003 | t0011 | g0301 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19043 | hp1 | a0003 | c0008 | t0008 | g0188 | AFR | LWK | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19043 | hp2 | a0003 | c0004 | t0003 | g0076 | AFR | LWK | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19056 | hp2 | a0004 | c0003 | t0005 | g0109 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19063 | hp1 | a0002 | c0005 | t0002 | g0293 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19065 | hp2 | a0004 | c0003 | t0004 | g0020 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19068 | hp1 | a0008 | c0019 | t0002 | g0312 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19074 | hp1 | a0002 | c0005 | t0002 | g0286 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19081 | hp2 | a0001 | c0011 | t0014 | g0332 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19088 | hp1 | a0004 | c0003 | t0011 | g0300 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | YRI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA19240 | hp2 | a0001 | c0010 | t0006 | g0330 | AFR | YRI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0236 | AFR | ASW | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20129 | hp2 | a0003 | c0015 | t0005 | g0118 | AFR | ASW | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0226 | EUR | TSI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20752 | hp2 | a0001 | c0001 | t0010 | g0013 | EUR | TSI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0242 | EUR | TSI | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | GIH | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | GIH | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02109 | hp1 | a0003 | c0004 | t0003 | g0127 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0260 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02486 | hp1 | a0001 | c0007 | t0002 | g0262 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02486 | hp2 | a0001 | c0007 | t0012 | g0006 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG02559 | hp2 | a0002 | c0006 | t0001 | g0103 | AFR | ACB | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03471 | hp1 | a0003 | c0004 | t0003 | g0181 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG06807 | hp1 | a0003 | c0008 | t0008 | g0001 | AFR | USA | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| HG06807 | hp2 | a0003 | c0014 | t0015 | g0024 | AFR | USA | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20300 | hp1 | a0003 | c0008 | t0008 | g0001 | AFR | USA | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0232 | AFR | USA | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0174 | REF | REF | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | TRIM16_chr17_15622966_15689311 | TRIM16 | chr17 | 15622966 | 15689311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15628628 | C | A | 1 | a0002 | 106 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
missense_variant | MODERATE | c.1682G>T | p.Gly561Val | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 2696/3358 | 1682/1695 | 561/564 | chr17 | 15628628 | |||
| chr17:15628770 | C | T | 1 | a0012 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1540G>A | p.Asp514Asn | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 2554/3358 | 1540/1695 | 514/564 | chr17 | 15628770 | |||
| chr17:15628818 | A | G | 1 | a0009 | 2 | HG02818.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.1492T>C | p.Tyr498His | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 2506/3358 | 1492/1695 | 498/564 | chr17 | 15628818 | |||
| chr17:15628833 | G | A | 2 | a0006 a0010 |
6 | HG00323.hp2 HG01952.hp2 HG01993.hp2 others(3): Show |
missense_variant | MODERATE | c.1477C>T | p.Arg493Trp | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 2491/3358 | 1477/1695 | 493/564 | chr17 | 15628833 | |||
| chr17:15632601 | G | A | 1 | a0007 | 3 | HG02257.hp2 HG02280.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.923C>T | p.Ser308Leu | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 10/12 | 1937/3358 | 923/1695 | 308/564 | chr17 | 15632601 | |||
| chr17:15636073 | C | G | 3 | a0004 a0005 a0008 |
26 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(23): Show |
missense_variant | MODERATE | c.812G>C | p.Arg271Thr | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/12 | 1826/3358 | 812/1695 | 271/564 | chr17 | 15636073 | |||
| chr17:15651247 | C | A | 5 | a0003 a0004 a0006 others(2): Show |
57 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(54): Show |
missense_variant | MODERATE | c.363G>T | p.Glu121Asp | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 1377/3358 | 363/1695 | 121/564 | chr17 | 15651247 | |||
| chr17:15651413 | C | T | 1 | a0011 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.197G>A | p.Gly66Glu | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 1211/3358 | 197/1695 | 66/564 | chr17 | 15651413 | |||
| chr17:15651467 | G | T | 1 | a0008 | 2 | HG00597.hp2 NA19068.hp1 |
stop_gained | HIGH | c.143C>A | p.Ser48* | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 1157/3358 | 143/1695 | 48/564 | chr17 | 15651467 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15628894 | G | A | 1 | a0002c0005 | 10 | HG00408.hp2 HG04184.hp2 NA18940.hp1 others(7): Show |
synonymous_variant | LOW | c.1416C>T | p.Asn472Asn | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 2430/3358 | 1416/1695 | 472/564 | chr17 | 15628894 | |||
| chr17:15628963 | G | A | 1 | a0001c0011 | 4 | HG01261.hp2 HG01433.hp1 NA18954.hp2 others(1): Show |
synonymous_variant | LOW | c.1347C>T | p.Ile449Ile | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 2361/3358 | 1347/1695 | 449/564 | chr17 | 15628963 | |||
| chr17:15629116 | G | A | 3 | a0003c0004 a0003c0017 a0009c0016 |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
synonymous_variant | LOW | c.1194C>T | p.Thr398Thr | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 2208/3358 | 1194/1695 | 398/564 | chr17 | 15629116 | |||
| chr17:15636090 | G | A | 5 | a0003c0025 a0004c0003 a0005c0012 others(2): Show |
27 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(24): Show |
synonymous_variant | LOW | c.795C>T | p.Ser265Ser | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/12 | 1809/3358 | 795/1695 | 265/564 | chr17 | 15636090 | |||
| chr17:15636246 | C | T | 6 | a0003c0008 a0003c0025 a0004c0003 others(3): Show |
32 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(29): Show |
synonymous_variant | LOW | c.639G>A | p.Ala213Ala | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/12 | 1653/3358 | 639/1695 | 213/564 | chr17 | 15636246 | |||
| chr17:15642757 | G | A | 1 | a0001c0024 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.579C>T | p.Ala193Ala | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/12 | 1593/3358 | 579/1695 | 193/564 | chr17 | 15642757 | |||
| chr17:15642769 | C | T | 2 | a0003c0008 a0003c0014 |
8 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(5): Show |
synonymous_variant | LOW | c.567G>A | p.Leu189Leu | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/12 | 1581/3358 | 567/1695 | 189/564 | chr17 | 15642769 | |||
| chr17:15651142 | C | T | 2 | a0001c0010 a0005c0021 |
5 | HG01934.hp2 HG02735.hp1 HG03453.hp2 others(2): Show |
synonymous_variant | LOW | c.468G>A | p.Glu156Glu | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 1482/3358 | 468/1695 | 156/564 | chr17 | 15651142 | |||
| chr17:15651190 | G | A | 5 | a0001c0007 a0002c0002 a0002c0005 others(2): Show |
108 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
synonymous_variant | LOW | c.420C>T | p.Ala140Ala | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 1434/3358 | 420/1695 | 140/564 | chr17 | 15651190 | |||
| chr17:15651384 | G | A | 1 | a0003c0017 | 2 | HG02970.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.226C>T | p.Leu76Leu | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 1240/3358 | 226/1695 | 76/564 | chr17 | 15651384 | |||
| chr17:15651478 | G | A | 1 | a0002c0026 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.132C>T | p.Asp44Asp | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 1146/3358 | 132/1695 | 44/564 | chr17 | 15651478 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15628120 | T | G | 1 | a0001c0001t0025 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*495A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 495 | chr17 | 15628120 | ||||||
| chr17:15628135 | C | T | 6 | a0001c0001t0025 a0003c0004t0003 a0003c0004t0024 others(3): Show |
19 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*480G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 480 | chr17 | 15628135 | ||||||
| chr17:15628408 | C | CA | 17 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0019 others(14): Show |
37 | HG00621.hp2 HG00738.hp2 HG01192.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*206dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 206 | chr17 | 15628408 | ||||||
| chr17:15628481 | A | T | 1 | a0001c0001t0019 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 134 | chr17 | 15628481 | ||||||
| chr17:15628551 | A | G | 1 | a0012c0022t0023 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 12/12 | 64 | chr17 | 15628551 | ||||||
| chr17:15651641 | T | C | 4 | a0005c0012t0016 a0005c0012t0020 a0005c0012t0027 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-32A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 32 | chr17 | 15651641 | ||||||
| chr17:15651775 | C | A | 1 | a0002c0002t0021 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-166G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 166 | chr17 | 15651775 | ||||||
| chr17:15651779 | G | A | 2 | a0004c0003t0011 a0004c0003t0026 |
4 | NA18960.hp1 NA18989.hp2 NA19007.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-170C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/12 | 170 | chr17 | 15651779 | ||||||
| chr17:15677182 | C | A | 7 | a0001c0001t0007 a0001c0007t0007 a0001c0024t0007 others(4): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-344G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/12 | chr17 | 15677182 | |||||||
| chr17:15677211 | A | G | 1 | a0002c0002t0022 | 1 | HG00741.hp2 | 5_prime_UTR_variant | MODIFIER | c.-373T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/12 | 25602 | chr17 | 15677211 | ||||||
| chr17:15677585 | C | G | 1 | a0001c0001t0018 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-453G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 5/12 | 25976 | chr17 | 15677585 | ||||||
| chr17:15680942 | C | T | 1 | a0001c0001t0010 | 3 | HG01255.hp2 HG01952.hp1 NA20752.hp2 |
5_prime_UTR_variant | MODIFIER | c.-667G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/12 | 29333 | chr17 | 15680942 | ||||||
| chr17:15684201 | C | T | 1 | a0001c0001t0013 | 2 | HG01257.hp1 HG01258.hp2 |
5_prime_UTR_variant | MODIFIER | c.-904G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/12 | 32592 | chr17 | 15684201 | ||||||
| chr17:15684216 | C | T | 1 | a0003c0017t0017 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-919G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/12 | 32607 | chr17 | 15684216 | ||||||
| chr17:15684261 | G | A | 27 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(24): Show |
157 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
5_prime_UTR_variant | MODIFIER | c.-964C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/12 | 32652 | chr17 | 15684261 | ||||||
| chr17:15684297 | A | T | 4 | a0002c0002t0009 a0003c0014t0015 a0005c0012t0016 others(1): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-1000T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/12 | 32688 | chr17 | 15684297 | ||||||
| chr17:15684300 | G | A | 4 | a0001c0001t0006 a0001c0010t0006 a0005c0012t0027 others(1): Show |
9 | HG01884.hp2 HG01934.hp2 HG02572.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-1003C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/12 | 32691 | chr17 | 15684300 | ||||||
| chr17:15684303 | G | A | 1 | a0001c0011t0014 | 2 | NA18954.hp2 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1006C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/12 | 32694 | chr17 | 15684303 | ||||||
| chr17:15684310 | A | G | 1 | a0001c0007t0012 | 2 | HG02486.hp2 HG02886.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1013T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/12 | 32701 | chr17 | 15684310 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15629377 | A | G | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1112-179T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15629377 | |||||||
| chr17:15629490 | C | A | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1112-292G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15629490 | |||||||
| chr17:15629578 | T | C | 18 | a0001c0001t0025g0249 a0003c0004t0003g0011 a0003c0004t0003g0072 others(15): Show |
19 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1112-380A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15629578 | |||||||
| chr17:15629662 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1112-464G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15629662 | |||||||
| chr17:15629771 | A | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0098 a0001c0001t0001g0100 others(4): Show |
7 | HG00741.hp1 HG01261.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-573T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15629771 | |||||||
| chr17:15629819 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1112-621G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15629819 | |||||||
| chr17:15629878 | C | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0065 |
2 | HG00438.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1112-680G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15629878 | |||||||
| chr17:15630085 | C | T | 4 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(1): Show |
4 | HG01934.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1112-887G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630085 | |||||||
| chr17:15630195 | C | G | 137 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(134): Show |
151 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1112-997G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630195 | |||||||
| chr17:15630219 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1112-1021G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630219 | |||||||
| chr17:15630285 | G | A | 1 | a0001c0007t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1112-1087C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630285 | |||||||
| chr17:15630342 | C | T | 1 | a0001c0001t0025g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1112-1144G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630342 | |||||||
| chr17:15630414 | T | A | 2 | a0004c0003t0001g0104 a0005c0021t0002g0253 |
2 | HG01070.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1111+1205A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630414 | |||||||
| chr17:15630441 | T | C | 1 | a0001c0001t0025g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1111+1178A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630441 | |||||||
| chr17:15630616 | C | A | 12 | a0002c0002t0001g0067 a0002c0002t0001g0142 a0002c0002t0001g0143 others(9): Show |
12 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.1111+1003G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630616 | |||||||
| chr17:15630658 | A | T | 101 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0002c0002t0001g0012 others(98): Show |
108 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1111+961T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630658 | |||||||
| chr17:15630659 | T | A | 4 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(1): Show |
4 | HG01934.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+960A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630659 | |||||||
| chr17:15630978 | T | C | 99 | a0002c0002t0001g0012 a0002c0002t0001g0049 a0002c0002t0001g0059 others(96): Show |
106 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1111+641A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15630978 | |||||||
| chr17:15631304 | T | C | 16 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(13): Show |
17 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1111+315A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15631304 | |||||||
| chr17:15631367 | C | T | 1 | a0001c0001t0025g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1111+252G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15631367 | |||||||
| chr17:15631503 | G | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1111+116C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 11/11 | chr17 | 15631503 | |||||||
| chr17:15631853 | C | T | 17 | a0002c0006t0001g0097 a0003c0004t0003g0011 a0003c0004t0003g0072 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1016-139G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 10/11 | chr17 | 15631853 | |||||||
| chr17:15631854 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1016-140C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 10/11 | chr17 | 15631854 | |||||||
| chr17:15632216 | C | T | 1 | a0003c0015t0004g0259 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1015+293G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 10/11 | chr17 | 15632216 | |||||||
| chr17:15632368 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1015+141G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 10/11 | chr17 | 15632368 | |||||||
| chr17:15632744 | A | T | 21 | a0001c0001t0005g0058 a0003c0025t0004g0313 a0004c0003t0004g0020 others(18): Show |
22 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.850-70T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15632744 | |||||||
| chr17:15632805 | ATGTGAAG | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(13): Show |
21 | HG00738.hp2 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-138_850-132del others(7): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15632805 | |||||||
| chr17:15632826 | G | T | 2 | a0001c0001t0002g0201 a0001c0001t0002g0204 |
2 | NA18956.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.850-152C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15632826 | |||||||
| chr17:15632849 | C | T | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.850-175G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15632849 | |||||||
| chr17:15632884 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.850-210A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15632884 | |||||||
| chr17:15633039 | C | G | 1 | a0001c0001t0002g0200 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.850-365G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633039 | |||||||
| chr17:15633271 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-597T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633271 | |||||||
| chr17:15633278 | C | A | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-604G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633278 | |||||||
| chr17:15633359 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0013g0195 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.850-685A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633359 | |||||||
| chr17:15633438 | A | T | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.850-764T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633438 | |||||||
| chr17:15633453 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-779G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633453 | |||||||
| chr17:15633460 | G | C | 21 | a0001c0001t0005g0058 a0003c0025t0004g0313 a0004c0003t0004g0020 others(18): Show |
22 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.850-786C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633460 | |||||||
| chr17:15633504 | G | A | 1 | a0001c0001t0025g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.850-830C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633504 | |||||||
| chr17:15633507 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-833T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633507 | |||||||
| chr17:15633511 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-837G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633511 | |||||||
| chr17:15633516 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.850-842A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633516 | |||||||
| chr17:15633540 | C | CT | 27 | a0001c0001t0001g0041 a0001c0001t0019g0123 a0001c0007t0002g0262 others(24): Show |
27 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.850-867dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633540 | |||||||
| chr17:15633540 | CT | C | 19 | a0001c0001t0001g0125 a0002c0006t0001g0175 a0003c0004t0003g0011 others(16): Show |
20 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.850-867delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633540 | |||||||
| chr17:15633571 | G | C | 1 | a0001c0001t0025g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.850-897C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633571 | |||||||
| chr17:15633603 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-929T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633603 | |||||||
| chr17:15633608 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-934G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633608 | |||||||
| chr17:15633667 | A | C | 6 | a0006c0009t0001g0106 a0006c0009t0001g0115 a0006c0009t0002g0213 others(3): Show |
6 | HG00323.hp2 HG01952.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-993T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633667 | |||||||
| chr17:15633690 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1016T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633690 | |||||||
| chr17:15633705 | T | A | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1031A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633705 | |||||||
| chr17:15633741 | C | T | 2 | a0003c0004t0003g0075 a0003c0004t0003g0076 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.850-1067G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633741 | |||||||
| chr17:15633785 | C | A | 1 | a0004c0003t0004g0297 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.850-1111G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633785 | |||||||
| chr17:15633829 | C | T | 4 | a0002c0002t0002g0017 a0002c0002t0002g0246 a0002c0002t0002g0247 others(1): Show |
5 | HG02083.hp1 NA18962.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-1155G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633829 | |||||||
| chr17:15633859 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
10 | HG01109.hp2 HG01891.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-1185T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633859 | |||||||
| chr17:15633880 | G | A | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1206C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633880 | |||||||
| chr17:15633926 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0107 |
2 | HG02155.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.850-1252C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633926 | |||||||
| chr17:15633961 | G | A | 1 | a0002c0002t0002g0308 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.850-1287C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633961 | |||||||
| chr17:15633977 | G | A | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1303C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15633977 | |||||||
| chr17:15634010 | T | C | 28 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(25): Show |
29 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.850-1336A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634010 | |||||||
| chr17:15634018 | C | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1344G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634018 | |||||||
| chr17:15634056 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1382T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634056 | |||||||
| chr17:15634067 | T | C | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1393A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634067 | |||||||
| chr17:15634146 | G | A | 1 | a0001c0007t0012g0006 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.850-1472C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634146 | |||||||
| chr17:15634157 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1483T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634157 | |||||||
| chr17:15634191 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1517G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634191 | |||||||
| chr17:15634198 | G | A | 1 | a0002c0002t0001g0172 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.850-1524C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634198 | |||||||
| chr17:15634221 | T | C | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1547A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634221 | |||||||
| chr17:15634224 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1550T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634224 | |||||||
| chr17:15634234 | C | T | 5 | a0001c0001t0019g0123 a0005c0012t0016g0023 a0005c0012t0020g0077 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-1560G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634234 | |||||||
| chr17:15634235 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1561T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634235 | |||||||
| chr17:15634246 | G | A | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1572C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634246 | |||||||
| chr17:15634260 | T | C | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1586A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634260 | |||||||
| chr17:15634268 | T | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1594A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634268 | |||||||
| chr17:15634278 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1604T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634278 | |||||||
| chr17:15634298 | T | C | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1624A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634298 | |||||||
| chr17:15634352 | G | A | 1 | a0002c0005t0002g0225 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.850-1678C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634352 | |||||||
| chr17:15634357 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1679G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634357 | |||||||
| chr17:15634365 | C | T | 2 | a0001c0007t0002g0262 a0001c0007t0007g0187 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.849+1671G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634365 | |||||||
| chr17:15634368 | T | G | 51 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0001c0001t0025g0249 others(48): Show |
53 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.849+1668A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634368 | |||||||
| chr17:15634370 | C | T | 11 | a0001c0001t0019g0123 a0005c0012t0016g0023 a0005c0012t0020g0077 others(8): Show |
11 | HG00323.hp2 HG01884.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+1666G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634370 | |||||||
| chr17:15634378 | G | C | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1658C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634378 | |||||||
| chr17:15634401 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
10 | HG01109.hp2 HG01891.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.849+1635C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634401 | |||||||
| chr17:15634435 | G | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1601C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634435 | |||||||
| chr17:15634487 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1549G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634487 | |||||||
| chr17:15634491 | C | T | 6 | a0006c0009t0001g0106 a0006c0009t0001g0115 a0006c0009t0002g0213 others(3): Show |
6 | HG00323.hp2 HG01952.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+1545G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634491 | |||||||
| chr17:15634520 | A | G | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1516T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634520 | |||||||
| chr17:15634545 | C | T | 5 | a0002c0002t0002g0215 a0002c0002t0002g0231 a0002c0002t0002g0236 others(2): Show |
5 | HG01106.hp1 HG01496.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+1491G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634545 | |||||||
| chr17:15634555 | C | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
8 | HG00438.hp1 HG00621.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+1481G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634555 | |||||||
| chr17:15634593 | T | C | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1443A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634593 | |||||||
| chr17:15634594 | G | A | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1442C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634594 | |||||||
| chr17:15634598 | T | G | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1438A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634598 | |||||||
| chr17:15634607 | G | C | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1429C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634607 | |||||||
| chr17:15634610 | A | T | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1426T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634610 | |||||||
| chr17:15634612 | C | T | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1424G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634612 | |||||||
| chr17:15634631 | C | CAA | 109 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(106): Show |
121 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.849+1403_849+1404d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634631 | |||||||
| chr17:15634631 | C | CAAAA | 11 | a0001c0001t0019g0123 a0005c0012t0016g0023 a0005c0012t0020g0077 others(8): Show |
11 | HG00323.hp2 HG01884.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+1401_849+1404d others(6): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634631 | |||||||
| chr17:15634631 | C | CAAAAA | 17 | a0001c0001t0005g0058 a0003c0025t0004g0313 a0004c0003t0001g0104 others(14): Show |
18 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.849+1400_849+1404d others(7): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634631 | |||||||
| chr17:15634639 | A | AT | 3 | a0001c0001t0025g0249 a0003c0004t0003g0181 a0003c0004t0003g0182 |
3 | HG03471.hp1 HG03579.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.849+1396_849+1397i others(3): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634639 | |||||||
| chr17:15634645 | A | AT | 14 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(11): Show |
15 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.849+1390_849+1391i others(3): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634645 | |||||||
| chr17:15634645 | A | T | 3 | a0001c0001t0025g0249 a0003c0004t0003g0181 a0003c0004t0003g0182 |
3 | HG03471.hp1 HG03579.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.849+1391T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634645 | |||||||
| chr17:15634647 | C | A | 17 | a0001c0001t0025g0249 a0003c0004t0003g0011 a0003c0004t0003g0072 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.849+1389G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634647 | |||||||
| chr17:15634681 | G | A | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.849+1355C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634681 | |||||||
| chr17:15634684 | T | C | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1352A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634684 | |||||||
| chr17:15634704 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1332G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634704 | |||||||
| chr17:15634731 | A | C | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1305T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634731 | |||||||
| chr17:15634735 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1301G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634735 | |||||||
| chr17:15634759 | C | T | 16 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(13): Show |
17 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.849+1277G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634759 | |||||||
| chr17:15634760 | G | A | 6 | a0001c0001t0002g0241 a0001c0001t0019g0123 a0005c0012t0016g0023 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+1276C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634760 | |||||||
| chr17:15634818 | A | AAC | 33 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(30): Show |
34 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.849+1216_849+1217d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634818 | |||||||
| chr17:15634829 | A | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(113): Show |
129 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.849+1207T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634829 | |||||||
| chr17:15634832 | A | C | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1204T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634832 | |||||||
| chr17:15634874 | T | G | 21 | a0001c0001t0005g0058 a0003c0025t0004g0313 a0004c0003t0004g0020 others(18): Show |
22 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.849+1162A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634874 | |||||||
| chr17:15634916 | A | G | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1120T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634916 | |||||||
| chr17:15634918 | G | A | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1118C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634918 | |||||||
| chr17:15634919 | C | G | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+1117G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634919 | |||||||
| chr17:15634954 | C | T | 165 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(162): Show |
180 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.849+1082G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634954 | |||||||
| chr17:15634966 | C | T | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1070G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634966 | |||||||
| chr17:15634968 | G | GA | 4 | a0003c0004t0003g0011 a0003c0004t0003g0168 a0003c0004t0003g0169 others(1): Show |
5 | HG02145.hp2 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+1067dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634968 | |||||||
| chr17:15634988 | G | A | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+1048C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15634988 | |||||||
| chr17:15635008 | G | A | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.849+1028C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635008 | |||||||
| chr17:15635058 | T | G | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+978A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635058 | |||||||
| chr17:15635059 | A | T | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.849+977T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635059 | |||||||
| chr17:15635067 | T | C | 1 | a0003c0025t0004g0313 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.849+969A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635067 | |||||||
| chr17:15635314 | T | C | 34 | a0001c0001t0005g0058 a0001c0001t0019g0123 a0003c0025t0004g0313 others(31): Show |
35 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+722A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635314 | |||||||
| chr17:15635336 | T | C | 22 | a0001c0001t0005g0058 a0003c0025t0004g0313 a0004c0003t0004g0020 others(19): Show |
23 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.849+700A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635336 | |||||||
| chr17:15635342 | G | A | 1 | a0001c0001t0006g0325 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.849+694C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635342 | |||||||
| chr17:15635388 | GATGTCTA others(50): Show |
G | 39 | a0001c0001t0001g0130 a0001c0001t0005g0058 a0001c0001t0019g0123 others(36): Show |
40 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.849+591_849+647del others(57): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635388 | |||||||
| chr17:15635404 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.849+632A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635404 | |||||||
| chr17:15635462 | T | C | 4 | a0002c0002t0001g0117 a0002c0002t0009g0022 a0002c0002t0009g0026 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+574A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635462 | |||||||
| chr17:15635845 | C | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG03471.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.849+191G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635845 | |||||||
| chr17:15635967 | T | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
29 | HG00738.hp2 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.849+69A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15635967 | |||||||
| chr17:15636013 | C | T | 9 | a0004c0003t0011g0299 a0004c0003t0011g0300 a0004c0003t0011g0301 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.849+23G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15636013 | |||||||
| chr17:15636023 | G | A | 9 | a0004c0003t0011g0299 a0004c0003t0011g0300 a0004c0003t0011g0301 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.849+13C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 9/11 | chr17 | 15636023 | |||||||
| chr17:15636275 | A | G | 26 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(23): Show |
27 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(24): Show |
splice_region_variant&intron_variant | LOW | c.616-6T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636275 | |||||||
| chr17:15636334 | A | G | 26 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(23): Show |
27 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.616-65T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636334 | |||||||
| chr17:15636353 | CAGCTTG | C | 26 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(23): Show |
27 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.616-90_616-85delCA others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636353 | |||||||
| chr17:15636449 | G | A | 1 | a0002c0002t0007g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.616-180C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636449 | |||||||
| chr17:15636483 | G | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-214C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636483 | |||||||
| chr17:15636505 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-236A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636505 | |||||||
| chr17:15636531 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-262G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636531 | |||||||
| chr17:15636557 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-288A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636557 | |||||||
| chr17:15636580 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-311A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636580 | |||||||
| chr17:15636630 | C | CT | 16 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0055 others(13): Show |
16 | HG01261.hp2 HG02055.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.616-362dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636630 | |||||||
| chr17:15636630 | CT | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(19): Show |
24 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.616-362delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636630 | |||||||
| chr17:15636630 | CTTTT | C | 29 | a0003c0025t0004g0313 a0004c0003t0004g0020 a0004c0003t0004g0202 others(26): Show |
30 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.616-365_616-362del others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636630 | |||||||
| chr17:15636791 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-522G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636791 | |||||||
| chr17:15636894 | G | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-625C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636894 | |||||||
| chr17:15636909 | C | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-640G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636909 | |||||||
| chr17:15636992 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-723A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15636992 | |||||||
| chr17:15637022 | TAAGAATT others(1245): Show |
T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2005_616-754de others(1): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637022 | |||||||
| chr17:15637051 | T | C | 37 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(34): Show |
44 | HG00738.hp2 HG01109.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.616-782A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637051 | |||||||
| chr17:15637078 | C | G | 2 | a0001c0007t0002g0262 a0001c0007t0007g0187 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.616-809G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637078 | |||||||
| chr17:15637084 | C | T | 1 | a0001c0001t0004g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.616-815G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637084 | |||||||
| chr17:15637085 | G | A | 1 | a0003c0004t0024g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.616-816C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637085 | |||||||
| chr17:15637104 | C | T | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.616-835G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637104 | |||||||
| chr17:15637115 | T | TG | 64 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0028 others(61): Show |
65 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.616-847dupC | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637115 | |||||||
| chr17:15637115 | T | TGG | 34 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(31): Show |
34 | HG00621.hp1 HG00642.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.616-848_616-847dup others(2): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637115 | |||||||
| chr17:15637115 | TG | T | 28 | a0001c0001t0001g0098 a0001c0001t0001g0131 a0001c0007t0001g0089 others(25): Show |
30 | HG00741.hp1 HG01168.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.616-847delC | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637115 | |||||||
| chr17:15637116 | G | T | 1 | a0002c0005t0001g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.616-847C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637116 | |||||||
| chr17:15637120 | G | C | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.616-851C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637120 | |||||||
| chr17:15637122 | G | GC | 4 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0038 others(1): Show |
6 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.616-854_616-853ins others(1): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637122 | |||||||
| chr17:15637125 | G | C | 4 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-856C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637125 | |||||||
| chr17:15637139 | C | G | 4 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(1): Show |
4 | HG01934.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-870G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637139 | |||||||
| chr17:15637155 | ATCCGGGA others(42): Show |
A | 5 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(2): Show |
5 | HG01934.hp2 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-935_616-887del others(49): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637155 | |||||||
| chr17:15637240 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0048 others(14): Show |
19 | HG00544.hp2 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.616-971C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637240 | |||||||
| chr17:15637256 | C | CGGGAGGT others(169): Show |
1 | a0003c0014t0005g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.616-988_616-987ins others(176): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637256 | |||||||
| chr17:15637271 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.616-1002C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637271 | |||||||
| chr17:15637314 | GCCCGGCC others(43): Show |
G | 1 | a0001c0007t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.616-1095_616-1046d others(52): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637314 | |||||||
| chr17:15637352 | G | GTCAGCCC others(168): Show |
2 | a0003c0008t0008g0001 a0003c0008t0008g0188 |
5 | HG01884.hp1 HG06807.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-1084_616-1083i others(177): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637352 | |||||||
| chr17:15637363 | T | C | 141 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0124 others(138): Show |
155 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.616-1094A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637363 | |||||||
| chr17:15637396 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.616-1127C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637396 | |||||||
| chr17:15637447 | C | A | 3 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 |
6 | HG00738.hp2 HG01884.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.616-1178G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637447 | |||||||
| chr17:15637447 | C | CGCCTCTG others(170): Show |
2 | a0003c0014t0008g0186 a0003c0014t0015g0024 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.616-1179_616-1178i others(179): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637447 | |||||||
| chr17:15637490 | T | TGCCCGGC others(42): Show |
1 | a0001c0001t0002g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.616-1270_616-1222d others(51): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637490 | |||||||
| chr17:15637490 | TGCCCGGC others(42): Show |
T | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.616-1270_616-1222d others(51): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637490 | |||||||
| chr17:15637512 | G | A | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.616-1243C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637512 | |||||||
| chr17:15637528 | G | T | 239 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
259 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.616-1259C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637528 | |||||||
| chr17:15637552 | G | A | 1 | a0002c0002t0002g0255 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.616-1283C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637552 | |||||||
| chr17:15637582 | GCCCCCCG others(45): Show |
G | 1 | a0001c0007t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.616-1365_616-1314d others(54): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637582 | |||||||
| chr17:15637604 | C | T | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | NA18942.hp2 NA18956.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-1335G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637604 | |||||||
| chr17:15637620 | TG | T | 18 | a0001c0001t0001g0033 a0003c0004t0003g0011 a0003c0004t0003g0072 others(15): Show |
19 | HG02027.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.616-1352delC | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637620 | |||||||
| chr17:15637640 | C | CG | 96 | a0001c0001t0001g0095 a0002c0002t0001g0012 a0002c0002t0001g0049 others(93): Show |
103 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.616-1372dupC | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637640 | |||||||
| chr17:15637640 | C | T | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.616-1371G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637640 | |||||||
| chr17:15637686 | G | A | 1 | a0002c0002t0002g0237 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.616-1417C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637686 | |||||||
| chr17:15637734 | C | G | 4 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(1): Show |
4 | HG01934.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-1465G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637734 | |||||||
| chr17:15637761 | T | C | 1 | a0002c0002t0002g0018 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.616-1492A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637761 | |||||||
| chr17:15637864 | G | A | 1 | a0002c0002t0002g0267 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.616-1595C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637864 | |||||||
| chr17:15637950 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.616-1681G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637950 | |||||||
| chr17:15637980 | T | G | 1 | a0002c0002t0002g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.616-1711A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15637980 | |||||||
| chr17:15638010 | G | A | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.616-1741C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638010 | |||||||
| chr17:15638057 | G | A | 2 | a0003c0008t0008g0001 a0003c0008t0008g0188 |
5 | HG01884.hp1 HG06807.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-1788C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638057 | |||||||
| chr17:15638076 | C | T | 4 | a0002c0002t0001g0142 a0002c0002t0001g0143 a0002c0002t0002g0290 others(1): Show |
4 | HG00423.hp1 NA18961.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-1807G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638076 | |||||||
| chr17:15638178 | T | G | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.616-1909A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638178 | |||||||
| chr17:15638255 | AT | A | 8 | a0001c0001t0001g0137 a0001c0001t0002g0252 a0001c0001t0002g0269 others(5): Show |
8 | HG01169.hp1 HG01934.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.616-1987delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638255 | |||||||
| chr17:15638257 | T | TAAAAAA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0167 others(7): Show |
12 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.616-1989_616-1988i others(8): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638257 | |||||||
| chr17:15638258 | T | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0124 others(28): Show |
34 | HG00408.hp1 HG00408.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.616-1989A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638258 | |||||||
| chr17:15638258 | T | TAAA | 14 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0075 others(11): Show |
15 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.616-1992_616-1990d others(5): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638258 | |||||||
| chr17:15638258 | TA | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(24): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.616-1990delT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638258 | |||||||
| chr17:15638291 | A | G | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.616-2022T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638291 | |||||||
| chr17:15638292 | GC | G | 5 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 others(2): Show |
8 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.616-2024delG | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638292 | |||||||
| chr17:15638294 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2025G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638294 | |||||||
| chr17:15638298 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2029A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638298 | |||||||
| chr17:15638300 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2031G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638300 | |||||||
| chr17:15638381 | G | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2112C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638381 | |||||||
| chr17:15638416 | C | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2147G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638416 | |||||||
| chr17:15638463 | C | CG | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2195_616-2194i others(3): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638463 | |||||||
| chr17:15638464 | A | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2195T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638464 | |||||||
| chr17:15638476 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.616-2207C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638476 | |||||||
| chr17:15638499 | A | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2230T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638499 | |||||||
| chr17:15638502 | G | A | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2233C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638502 | |||||||
| chr17:15638593 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2324G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638593 | |||||||
| chr17:15638594 | A | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2325T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638594 | |||||||
| chr17:15638615 | C | A | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2346G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638615 | |||||||
| chr17:15638650 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2381A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638650 | |||||||
| chr17:15638691 | T | A | 1 | a0001c0001t0002g0320 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.616-2422A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638691 | |||||||
| chr17:15638760 | T | G | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.616-2491A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638760 | |||||||
| chr17:15638920 | T | A | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.616-2651A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15638920 | |||||||
| chr17:15639019 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(13): Show |
21 | HG00738.hp2 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.616-2750T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639019 | |||||||
| chr17:15639035 | T | TTC | 4 | a0006c0009t0001g0115 a0006c0009t0002g0214 a0006c0009t0002g0295 others(1): Show |
4 | HG00323.hp2 HG01993.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-2768_616-2767d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639035 | |||||||
| chr17:15639045 | C | CT | 35 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0053 others(32): Show |
35 | HG00639.hp1 HG00735.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.616-2777dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639045 | |||||||
| chr17:15639045 | CT | C | 29 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0132 others(26): Show |
33 | HG00738.hp2 HG01070.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.616-2777delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639045 | |||||||
| chr17:15639045 | CTT | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(23): Show |
29 | HG01070.hp2 HG01109.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.616-2778_616-2777d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639045 | |||||||
| chr17:15639046 | T | TC | 8 | a0001c0001t0001g0129 a0001c0001t0001g0140 a0001c0001t0001g0152 others(5): Show |
8 | HG00621.hp2 HG01175.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.616-2778_616-2777i others(3): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639046 | |||||||
| chr17:15639047 | T | C | 56 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0033 others(53): Show |
60 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.616-2778A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639047 | |||||||
| chr17:15639048 | T | C | 7 | a0001c0001t0001g0045 a0001c0001t0001g0132 a0001c0001t0001g0153 others(4): Show |
7 | HG01496.hp2 HG01884.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.616-2779A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639048 | |||||||
| chr17:15639049 | T | C | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.616-2780A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639049 | |||||||
| chr17:15639072 | T | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-2803A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639072 | |||||||
| chr17:15639106 | G | A | 49 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(46): Show |
51 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.616-2837C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639106 | |||||||
| chr17:15639111 | G | A | 49 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(46): Show |
51 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.616-2842C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639111 | |||||||
| chr17:15639150 | G | A | 7 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 others(4): Show |
10 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.616-2881C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639150 | |||||||
| chr17:15639189 | G | A | 1 | a0007c0013t0009g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.616-2920C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639189 | |||||||
| chr17:15639203 | G | A | 4 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(1): Show |
4 | HG01934.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-2934C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639203 | |||||||
| chr17:15639227 | G | A | 1 | a0001c0007t0012g0006 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.616-2958C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639227 | |||||||
| chr17:15639285 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(13): Show |
21 | HG00738.hp2 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.616-3016T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639285 | |||||||
| chr17:15639361 | T | C | 1 | a0003c0015t0004g0259 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.616-3092A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639361 | |||||||
| chr17:15639383 | G | A | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-3114C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639383 | |||||||
| chr17:15639385 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-3116A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639385 | |||||||
| chr17:15639448 | C | T | 49 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(46): Show |
51 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.616-3179G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639448 | |||||||
| chr17:15639479 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.616-3210A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639479 | |||||||
| chr17:15639521 | C | G | 1 | a0001c0010t0006g0331 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.615+3200G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639521 | |||||||
| chr17:15639602 | G | A | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.615+3119C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639602 | |||||||
| chr17:15639610 | G | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+3111C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639610 | |||||||
| chr17:15639615 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+3106G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639615 | |||||||
| chr17:15639619 | A | G | 49 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(46): Show |
51 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.615+3102T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639619 | |||||||
| chr17:15639688 | G | C | 1 | a0004c0003t0004g0319 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.615+3033C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639688 | |||||||
| chr17:15639813 | A | T | 1 | a0001c0024t0007g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.615+2908T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639813 | |||||||
| chr17:15639847 | T | C | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2874A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639847 | |||||||
| chr17:15639849 | T | C | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2872A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639849 | |||||||
| chr17:15639850 | A | T | 31 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(28): Show |
32 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.615+2871T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639850 | |||||||
| chr17:15639851 | G | C | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2870C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639851 | |||||||
| chr17:15639854 | T | G | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2867A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639854 | |||||||
| chr17:15639856 | T | G | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2865A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639856 | |||||||
| chr17:15639857 | G | C | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2864C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639857 | |||||||
| chr17:15639858 | C | T | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2863G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639858 | |||||||
| chr17:15639860 | G | T | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2861C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639860 | |||||||
| chr17:15639861 | C | A | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2860G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639861 | |||||||
| chr17:15639862 | C | T | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2859G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639862 | |||||||
| chr17:15639863 | C | T | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.615+2858G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639863 | |||||||
| chr17:15639913 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+2808G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639913 | |||||||
| chr17:15639940 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+2781G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15639940 | |||||||
| chr17:15640069 | A | G | 49 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(46): Show |
51 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.615+2652T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640069 | |||||||
| chr17:15640109 | GC | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+2611delG | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640109 | |||||||
| chr17:15640148 | T | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+2573A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640148 | |||||||
| chr17:15640163 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+2558A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640163 | |||||||
| chr17:15640213 | A | G | 2 | a0002c0002t0002g0246 a0002c0002t0002g0247 |
2 | NA19054.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.615+2508T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640213 | |||||||
| chr17:15640226 | G | C | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.615+2495C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640226 | |||||||
| chr17:15640336 | G | A | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.615+2385C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640336 | |||||||
| chr17:15640339 | G | C | 1 | a0002c0002t0001g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.615+2382C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640339 | |||||||
| chr17:15640388 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+2333G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640388 | |||||||
| chr17:15640398 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+2323A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640398 | |||||||
| chr17:15640448 | C | T | 4 | a0005c0012t0016g0023 a0005c0012t0020g0077 a0005c0012t0027g0328 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.615+2273G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640448 | |||||||
| chr17:15640475 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0088 a0001c0001t0001g0140 others(2): Show |
5 | HG00544.hp2 HG02027.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+2246A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640475 | |||||||
| chr17:15640507 | G | C | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.615+2214C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640507 | |||||||
| chr17:15640627 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+2094G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640627 | |||||||
| chr17:15640687 | G | A | 1 | a0003c0017t0003g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.615+2034C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640687 | |||||||
| chr17:15640733 | A | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1988T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640733 | |||||||
| chr17:15640780 | C | T | 2 | a0001c0007t0012g0006 a0003c0015t0001g0105 |
3 | HG02486.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.615+1941G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640780 | |||||||
| chr17:15640864 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1857A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640864 | |||||||
| chr17:15640866 | C | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1855G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640866 | |||||||
| chr17:15640997 | C | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1724G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15640997 | |||||||
| chr17:15641012 | G | GC | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1708_615+1709i others(3): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641012 | |||||||
| chr17:15641033 | A | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1688T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641033 | |||||||
| chr17:15641053 | C | T | 1 | a0003c0004t0003g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.615+1668G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641053 | |||||||
| chr17:15641224 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1497A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641224 | |||||||
| chr17:15641246 | C | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1475G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641246 | |||||||
| chr17:15641251 | C | T | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.615+1470G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641251 | |||||||
| chr17:15641262 | GGCCTCAA others(12): Show |
G | 1 | a0003c0015t0005g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.615+1440_615+1458d others(21): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641262 | |||||||
| chr17:15641285 | A | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1436T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641285 | |||||||
| chr17:15641312 | A | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1409T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641312 | |||||||
| chr17:15641330 | A | G | 7 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 others(4): Show |
10 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.615+1391T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641330 | |||||||
| chr17:15641350 | A | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1371T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641350 | |||||||
| chr17:15641387 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1334A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641387 | |||||||
| chr17:15641451 | T | C | 3 | a0001c0007t0002g0258 a0003c0004t0003g0181 a0003c0004t0003g0182 |
3 | HG02258.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.615+1270A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641451 | |||||||
| chr17:15641467 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1254A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641467 | |||||||
| chr17:15641469 | C | A | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1252G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641469 | |||||||
| chr17:15641482 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.615+1239A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641482 | |||||||
| chr17:15641594 | A | G | 6 | a0001c0001t0001g0095 a0002c0006t0001g0082 a0002c0006t0001g0096 others(3): Show |
6 | HG01192.hp2 HG01243.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+1127T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641594 | |||||||
| chr17:15641613 | G | A | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1108C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641613 | |||||||
| chr17:15641728 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.615+993C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641728 | |||||||
| chr17:15641768 | G | A | 1 | a0003c0015t0001g0105 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615+953C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641768 | |||||||
| chr17:15641889 | C | G | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+832G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15641889 | |||||||
| chr17:15642033 | A | G | 49 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(46): Show |
51 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.615+688T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642033 | |||||||
| chr17:15642064 | G | A | 34 | a0001c0007t0012g0006 a0003c0015t0001g0105 a0003c0025t0004g0313 others(31): Show |
36 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.615+657C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642064 | |||||||
| chr17:15642124 | G | A | 88 | a0002c0002t0001g0012 a0002c0002t0001g0049 a0002c0002t0001g0059 others(85): Show |
95 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.615+597C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642124 | |||||||
| chr17:15642189 | T | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+532A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642189 | |||||||
| chr17:15642277 | A | T | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.615+444T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642277 | |||||||
| chr17:15642281 | G | C | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+440C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642281 | |||||||
| chr17:15642284 | A | G | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.615+437T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642284 | |||||||
| chr17:15642348 | G | T | 1 | a0003c0017t0003g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.615+373C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642348 | |||||||
| chr17:15642358 | A | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+363T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642358 | |||||||
| chr17:15642380 | A | T | 32 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(29): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+341T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642380 | |||||||
| chr17:15642489 | A | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(13): Show |
21 | HG00738.hp2 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.615+232T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642489 | |||||||
| chr17:15642587 | C | T | 1 | a0003c0015t0004g0259 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.615+134G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642587 | |||||||
| chr17:15642589 | G | C | 29 | a0001c0001t0002g0264 a0003c0025t0004g0313 a0004c0003t0001g0104 others(26): Show |
30 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.615+132C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642589 | |||||||
| chr17:15642592 | T | C | 29 | a0001c0001t0002g0264 a0003c0025t0004g0313 a0004c0003t0001g0104 others(26): Show |
30 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.615+129A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 8/11 | chr17 | 15642592 | |||||||
| chr17:15642818 | T | TA | 19 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(16): Show |
20 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.520-3dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15642818 | |||||||
| chr17:15642825 | G | A | 22 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(19): Show |
23 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.520-9C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15642825 | |||||||
| chr17:15642887 | G | A | 1 | a0001c0007t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.520-71C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15642887 | |||||||
| chr17:15642897 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.520-81G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15642897 | |||||||
| chr17:15642956 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.520-140C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15642956 | |||||||
| chr17:15642964 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.520-148G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15642964 | |||||||
| chr17:15643019 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.520-203G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643019 | |||||||
| chr17:15643099 | C | T | 1 | a0002c0002t0002g0294 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.520-283G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643099 | |||||||
| chr17:15643133 | A | AG | 69 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(66): Show |
77 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.520-318_520-317ins others(1): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643133 | |||||||
| chr17:15643134 | A | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(66): Show |
77 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.520-318T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643134 | |||||||
| chr17:15643148 | G | C | 4 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(1): Show |
4 | HG01934.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-332C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643148 | |||||||
| chr17:15643287 | G | T | 1 | a0001c0001t0002g0228 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.520-471C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643287 | |||||||
| chr17:15643388 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.520-572G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643388 | |||||||
| chr17:15643471 | C | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(66): Show |
77 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.520-655G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643471 | |||||||
| chr17:15643598 | A | G | 21 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(18): Show |
22 | HG01070.hp2 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.520-782T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643598 | |||||||
| chr17:15643678 | G | A | 1 | a0002c0026t0002g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.520-862C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643678 | |||||||
| chr17:15643921 | T | A | 1 | a0002c0002t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.520-1105A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15643921 | |||||||
| chr17:15644044 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1228C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644044 | |||||||
| chr17:15644114 | G | C | 6 | a0006c0009t0001g0106 a0006c0009t0001g0115 a0006c0009t0002g0213 others(3): Show |
6 | HG00323.hp2 HG01952.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-1298C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644114 | |||||||
| chr17:15644516 | T | A | 1 | a0012c0022t0023g0223 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.520-1700A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644516 | |||||||
| chr17:15644530 | T | C | 2 | a0006c0009t0001g0106 a0006c0009t0001g0115 |
2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.520-1714A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644530 | |||||||
| chr17:15644681 | G | GC | 22 | a0003c0025t0004g0313 a0004c0003t0001g0104 a0004c0003t0004g0020 others(19): Show |
23 | HG00597.hp2 HG00621.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.520-1866dupG | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644681 | |||||||
| chr17:15644760 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(15): Show |
24 | HG00738.hp2 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.520-1944C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644760 | |||||||
| chr17:15644816 | G | GTTC | 19 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(16): Show |
20 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.520-2003_520-2001d others(5): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644816 | |||||||
| chr17:15644854 | C | T | 3 | a0003c0004t0024g0257 a0009c0016t0003g0126 a0009c0016t0003g0128 |
3 | HG02818.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.520-2038G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644854 | |||||||
| chr17:15644908 | C | T | 29 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(26): Show |
30 | HG00323.hp2 HG01884.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.520-2092G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644908 | |||||||
| chr17:15644916 | T | C | 29 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(26): Show |
30 | HG00323.hp2 HG01884.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.520-2100A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644916 | |||||||
| chr17:15644919 | G | A | 29 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(26): Show |
30 | HG00323.hp2 HG01884.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.520-2103C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644919 | |||||||
| chr17:15644954 | T | C | 10 | a0005c0012t0016g0023 a0005c0012t0020g0077 a0005c0012t0027g0328 others(7): Show |
10 | HG00323.hp2 HG01884.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-2138A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644954 | |||||||
| chr17:15644968 | G | A | 29 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(26): Show |
30 | HG00323.hp2 HG01884.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.520-2152C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15644968 | |||||||
| chr17:15645266 | A | G | 1 | a0002c0002t0002g0232 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.520-2450T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645266 | |||||||
| chr17:15645304 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.520-2488C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645304 | |||||||
| chr17:15645378 | C | T | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.520-2562G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645378 | |||||||
| chr17:15645475 | T | C | 19 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(16): Show |
20 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.520-2659A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645475 | |||||||
| chr17:15645496 | G | A | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.520-2680C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645496 | |||||||
| chr17:15645538 | T | G | 4 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-2722A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645538 | |||||||
| chr17:15645571 | G | T | 2 | a0001c0001t0007g0192 a0001c0001t0007g0193 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.520-2755C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645571 | |||||||
| chr17:15645571 | GA | G | 7 | a0001c0001t0001g0154 a0001c0007t0002g0254 a0001c0007t0002g0258 others(4): Show |
7 | HG00735.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-2756delT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645571 | |||||||
| chr17:15645571 | GAA | G | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.520-2757_520-2756d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645571 | |||||||
| chr17:15645599 | C | CTT | 57 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(54): Show |
65 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.520-2785_520-2784d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645599 | |||||||
| chr17:15645668 | T | C | 6 | a0006c0009t0001g0106 a0006c0009t0001g0115 a0006c0009t0002g0213 others(3): Show |
6 | HG00323.hp2 HG01952.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-2852A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645668 | |||||||
| chr17:15645732 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0152 others(3): Show |
8 | HG00642.hp1 HG00738.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-2916T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645732 | |||||||
| chr17:15645739 | G | A | 17 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.520-2923C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15645739 | |||||||
| chr17:15646078 | C | A | 7 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 others(4): Show |
10 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-3262G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646078 | |||||||
| chr17:15646171 | A | G | 1 | a0001c0001t0018g0090 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.520-3355T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646171 | |||||||
| chr17:15646193 | G | A | 6 | a0006c0009t0001g0106 a0006c0009t0001g0115 a0006c0009t0002g0213 others(3): Show |
6 | HG00323.hp2 HG01952.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-3377C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646193 | |||||||
| chr17:15646254 | A | G | 166 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(163): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.520-3438T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646254 | |||||||
| chr17:15646256 | C | T | 1 | a0001c0001t0002g0275 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.520-3440G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646256 | |||||||
| chr17:15646370 | G | T | 2 | a0003c0004t0003g0075 a0003c0004t0003g0076 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.520-3554C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646370 | |||||||
| chr17:15646409 | G | A | 9 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0098 others(6): Show |
9 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.520-3593C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646409 | |||||||
| chr17:15646441 | A | C | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.520-3625T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646441 | |||||||
| chr17:15646526 | C | T | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.520-3710G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646526 | |||||||
| chr17:15646578 | T | C | 40 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0004t0003g0011 others(37): Show |
42 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.520-3762A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646578 | |||||||
| chr17:15646680 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(162): Show |
180 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.520-3864T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646680 | |||||||
| chr17:15646777 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.520-3961T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646777 | |||||||
| chr17:15646782 | G | C | 2 | a0001c0007t0002g0262 a0001c0007t0007g0187 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.520-3966C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15646782 | |||||||
| chr17:15647027 | C | T | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.519+4064G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647027 | |||||||
| chr17:15647129 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.519+3962C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647129 | |||||||
| chr17:15647156 | T | A | 1 | a0004c0003t0004g0303 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.519+3935A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647156 | |||||||
| chr17:15647212 | TCCACCCG others(37): Show |
T | 4 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(1): Show |
4 | HG01934.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+3835_519+3878d others(46): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647212 | |||||||
| chr17:15647360 | G | A | 3 | a0003c0014t0005g0112 a0003c0014t0008g0186 a0003c0014t0015g0024 |
3 | HG00738.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.519+3731C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647360 | |||||||
| chr17:15647371 | G | A | 2 | a0001c0007t0012g0006 a0003c0015t0001g0105 |
3 | HG02486.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.519+3720C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647371 | |||||||
| chr17:15647446 | C | T | 1 | a0002c0002t0001g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.519+3645G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647446 | |||||||
| chr17:15647564 | C | T | 3 | a0002c0002t0001g0012 a0002c0002t0001g0170 a0002c0002t0001g0171 |
4 | HG02559.hp1 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+3527G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647564 | |||||||
| chr17:15647603 | G | A | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.519+3488C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647603 | |||||||
| chr17:15647816 | T | TAC | 25 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0042 others(22): Show |
26 | HG00438.hp2 HG01106.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.519+3273_519+3274d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | T | TACAC | 88 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0095 others(85): Show |
96 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.519+3271_519+3274d others(6): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | T | TACACAC | 30 | a0001c0001t0001g0036 a0002c0002t0001g0119 a0002c0002t0001g0144 others(27): Show |
31 | HG00423.hp1 HG00673.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.519+3269_519+3274d others(8): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | T | TACACACA others(1): Show |
10 | a0001c0007t0012g0006 a0001c0011t0001g0094 a0002c0005t0002g0286 others(7): Show |
11 | HG01070.hp2 HG01261.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+3267_519+3274d others(10): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | T | TACACACA others(3): Show |
5 | a0001c0010t0006g0323 a0003c0017t0017g0027 a0005c0012t0027g0328 others(2): Show |
5 | HG01884.hp2 HG01952.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+3265_519+3274d others(12): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | T | TACACACA others(5): Show |
2 | a0002c0002t0002g0261 a0006c0009t0002g0214 |
2 | HG01993.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.519+3263_519+3274d others(14): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | T | TACACACA others(7): Show |
3 | a0001c0007t0002g0262 a0001c0010t0006g0326 a0001c0010t0006g0330 |
3 | HG02486.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.519+3261_519+3274d others(16): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | T | TACACACA others(9): Show |
4 | a0001c0007t0001g0089 a0001c0007t0007g0187 a0001c0010t0006g0331 others(1): Show |
4 | HG01934.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+3259_519+3274d others(18): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | T | TACACACA others(13): Show |
1 | a0006c0009t0001g0115 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.519+3255_519+3274d others(22): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | TACAC | T | 20 | a0003c0025t0004g0313 a0004c0003t0004g0020 a0004c0003t0004g0202 others(17): Show |
21 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.519+3271_519+3274d others(6): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | TACACACA others(1): Show |
T | 6 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 others(3): Show |
9 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+3267_519+3274d others(10): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647816 | TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+3265_519+3274d others(12): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647816 | |||||||
| chr17:15647851 | A | ACACACAC others(11): Show |
4 | a0002c0002t0001g0111 a0002c0002t0002g0263 a0002c0002t0002g0266 others(1): Show |
4 | HG03654.hp1 HG04184.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+3239_519+3240i others(20): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647851 | |||||||
| chr17:15647938 | A | G | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.519+3153T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647938 | |||||||
| chr17:15647947 | C | T | 3 | a0002c0006t0001g0175 a0002c0006t0001g0179 a0002c0006t0001g0180 |
3 | HG01168.hp2 HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.519+3144G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647947 | |||||||
| chr17:15647966 | C | T | 4 | a0005c0012t0016g0023 a0005c0012t0020g0077 a0005c0012t0027g0328 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+3125G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15647966 | |||||||
| chr17:15648012 | T | C | 1 | a0009c0016t0003g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.519+3079A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648012 | |||||||
| chr17:15648082 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0122 others(2): Show |
6 | NA18956.hp1 NA18963.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+3009G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648082 | |||||||
| chr17:15648118 | C | G | 4 | a0005c0012t0016g0023 a0005c0012t0020g0077 a0005c0012t0027g0328 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+2973G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648118 | |||||||
| chr17:15648119 | G | A | 1 | a0003c0015t0004g0259 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.519+2972C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648119 | |||||||
| chr17:15648225 | C | CA | 7 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0041 others(4): Show |
7 | HG00639.hp2 HG01109.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.519+2865dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648225 | |||||||
| chr17:15648225 | CA | C | 54 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(51): Show |
60 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.519+2865delT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648225 | |||||||
| chr17:15648234 | A | C | 2 | a0002c0002t0002g0272 a0002c0002t0002g0273 |
2 | HG00673.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.519+2857T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648234 | |||||||
| chr17:15648240 | A | C | 1 | a0004c0003t0011g0299 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.519+2851T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648240 | |||||||
| chr17:15648241 | C | A | 2 | a0001c0001t0001g0086 a0004c0003t0011g0299 |
2 | NA18960.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.519+2850G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648241 | |||||||
| chr17:15648244 | A | C | 1 | a0004c0003t0011g0299 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.519+2847T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648244 | |||||||
| chr17:15648259 | AC | A | 12 | a0003c0004t0003g0011 a0003c0004t0003g0075 a0003c0004t0003g0076 others(9): Show |
13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.519+2831delG | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648259 | |||||||
| chr17:15648260 | C | A | 6 | a0002c0002t0002g0234 a0006c0009t0001g0106 a0006c0009t0001g0115 others(3): Show |
6 | HG01952.hp2 HG01993.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+2831G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648260 | |||||||
| chr17:15648260 | C | CA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(33): Show |
38 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.519+2830dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648260 | |||||||
| chr17:15648263 | AC | A | 11 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0002c0002t0001g0119 others(8): Show |
11 | HG01070.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+2827delG | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648263 | |||||||
| chr17:15648264 | C | A | 150 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(147): Show |
161 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.519+2827G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648264 | |||||||
| chr17:15648264 | C | CAA | 2 | a0003c0008t0008g0001 a0003c0008t0008g0188 |
5 | HG01884.hp1 HG06807.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+2825_519+2826d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648264 | |||||||
| chr17:15648271 | A | C | 1 | a0002c0002t0002g0231 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.519+2820T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648271 | |||||||
| chr17:15648557 | G | T | 90 | a0002c0002t0001g0012 a0002c0002t0001g0049 a0002c0002t0001g0059 others(87): Show |
97 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.519+2534C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648557 | |||||||
| chr17:15648880 | C | T | 6 | a0004c0003t0001g0104 a0006c0009t0001g0106 a0006c0009t0001g0115 others(3): Show |
6 | HG01070.hp2 HG01952.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+2211G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648880 | |||||||
| chr17:15648896 | A | G | 1 | a0004c0003t0005g0109 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.519+2195T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15648896 | |||||||
| chr17:15649179 | TAAG | T | 27 | a0001c0007t0012g0006 a0001c0010t0006g0323 a0001c0010t0006g0326 others(24): Show |
29 | HG01884.hp2 HG01934.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.519+1909_519+1911d others(5): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649179 | |||||||
| chr17:15649274 | G | A | 93 | a0001c0007t0001g0089 a0001c0007t0002g0262 a0001c0007t0007g0187 others(90): Show |
100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.519+1817C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649274 | |||||||
| chr17:15649427 | C | T | 1 | a0004c0003t0004g0202 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.519+1664G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649427 | |||||||
| chr17:15649431 | C | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+1660G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649431 | |||||||
| chr17:15649432 | G | A | 1 | a0002c0006t0001g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.519+1659C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649432 | |||||||
| chr17:15649467 | T | C | 8 | a0003c0004t0003g0072 a0003c0004t0003g0073 a0003c0004t0003g0078 others(5): Show |
8 | HG02109.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+1624A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649467 | |||||||
| chr17:15649528 | T | A | 5 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 others(2): Show |
8 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+1563A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649528 | |||||||
| chr17:15649589 | G | A | 93 | a0001c0007t0001g0089 a0001c0007t0002g0262 a0001c0007t0007g0187 others(90): Show |
100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.519+1502C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649589 | |||||||
| chr17:15649700 | T | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0062 others(29): Show |
34 | HG00558.hp2 HG00609.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.519+1391A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649700 | |||||||
| chr17:15649802 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+1289C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649802 | |||||||
| chr17:15649905 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+1186A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15649905 | |||||||
| chr17:15650046 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(1): Show |
5 | HG03195.hp2 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+1045A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15650046 | |||||||
| chr17:15650168 | G | A | 1 | a0001c0024t0007g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.519+923C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15650168 | |||||||
| chr17:15650395 | C | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(162): Show |
180 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.519+696G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15650395 | |||||||
| chr17:15650737 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.519+354T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15650737 | |||||||
| chr17:15650859 | G | A | 52 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(49): Show |
57 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.519+232C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15650859 | |||||||
| chr17:15650964 | A | G | 166 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(163): Show |
181 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.519+127T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15650964 | |||||||
| chr17:15650998 | A | G | 1 | a0001c0001t0005g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.519+93T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 7/11 | chr17 | 15650998 | |||||||
| chr17:15652150 | C | CT | 88 | a0001c0001t0002g0248 a0002c0002t0001g0012 a0002c0002t0001g0049 others(85): Show |
95 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-337-205dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652150 | |||||||
| chr17:15652150 | C | CTT | 6 | a0002c0002t0002g0239 a0002c0005t0001g0068 a0005c0012t0016g0023 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-337-206_-337-205d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652150 | |||||||
| chr17:15652150 | CT | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0001t0001g0124 others(8): Show |
13 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-337-205delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652150 | |||||||
| chr17:15652155 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0136 a0001c0001t0002g0305 others(3): Show |
6 | HG02486.hp1 HG02922.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.-337-209A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652155 | |||||||
| chr17:15652318 | C | CT | 17 | a0001c0001t0005g0058 a0003c0004t0003g0011 a0003c0004t0003g0072 others(14): Show |
18 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-337-373dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652318 | |||||||
| chr17:15652318 | CT | C | 215 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(212): Show |
233 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.-337-373delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652318 | |||||||
| chr17:15652318 | CTT | C | 7 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(4): Show |
8 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-337-374_-337-373d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652318 | |||||||
| chr17:15652455 | C | CT | 83 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0040 others(80): Show |
89 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-337-510dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652455 | |||||||
| chr17:15652455 | C | CTT | 78 | a0001c0001t0001g0004 a0001c0001t0001g0081 a0001c0001t0001g0125 others(75): Show |
86 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-337-511_-337-510d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652455 | |||||||
| chr17:15652455 | C | CTTT | 36 | a0001c0001t0001g0124 a0001c0007t0002g0262 a0001c0010t0006g0326 others(33): Show |
37 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-337-512_-337-510d others(5): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652455 | |||||||
| chr17:15652459 | T | G | 1 | a0001c0001t0007g0194 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-337-513A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652459 | |||||||
| chr17:15652460 | T | G | 2 | a0001c0001t0007g0192 a0001c0001t0007g0193 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-337-514A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652460 | |||||||
| chr17:15652614 | C | G | 7 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(4): Show |
8 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-337-668G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652614 | |||||||
| chr17:15652663 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0136 |
2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-337-717C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652663 | |||||||
| chr17:15652680 | C | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
5 | NA18953.hp2 NA18972.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.-337-734G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652680 | |||||||
| chr17:15652712 | G | A | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-337-766C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652712 | |||||||
| chr17:15652736 | C | T | 57 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(54): Show |
62 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.-337-790G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652736 | |||||||
| chr17:15652815 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-337-869A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652815 | |||||||
| chr17:15652849 | G | A | 1 | a0001c0024t0007g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-337-903C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15652849 | |||||||
| chr17:15653080 | C | T | 1 | a0003c0015t0001g0105 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-337-1134G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653080 | |||||||
| chr17:15653113 | G | T | 1 | a0002c0002t0002g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-337-1167C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653113 | |||||||
| chr17:15653297 | C | T | 5 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(2): Show |
5 | HG01934.hp2 HG02735.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-337-1351G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653297 | |||||||
| chr17:15653308 | G | A | 2 | a0002c0002t0009g0022 a0002c0002t0009g0026 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-337-1362C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653308 | |||||||
| chr17:15653337 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-1391C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653337 | |||||||
| chr17:15653348 | C | T | 1 | a0001c0007t0012g0006 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-337-1402G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653348 | |||||||
| chr17:15653356 | G | A | 93 | a0001c0007t0001g0089 a0001c0007t0002g0262 a0001c0007t0007g0187 others(90): Show |
100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-337-1410C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653356 | |||||||
| chr17:15653831 | G | A | 1 | a0002c0005t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-337-1885C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653831 | |||||||
| chr17:15653844 | G | A | 1 | a0003c0008t0008g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-337-1898C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653844 | |||||||
| chr17:15653853 | G | A | 2 | a0003c0004t0003g0075 a0003c0004t0003g0076 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-337-1907C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653853 | |||||||
| chr17:15653982 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-2036C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653982 | |||||||
| chr17:15653985 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-2039A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15653985 | |||||||
| chr17:15654020 | C | T | 2 | a0003c0014t0005g0112 a0003c0014t0015g0024 |
2 | HG00738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-337-2074G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654020 | |||||||
| chr17:15654110 | G | A | 93 | a0001c0007t0001g0089 a0001c0007t0002g0262 a0001c0007t0007g0187 others(90): Show |
100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-337-2164C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654110 | |||||||
| chr17:15654194 | C | T | 52 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(49): Show |
57 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.-337-2248G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654194 | |||||||
| chr17:15654216 | G | C | 90 | a0002c0002t0001g0012 a0002c0002t0001g0049 a0002c0002t0001g0059 others(87): Show |
97 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-337-2270C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654216 | |||||||
| chr17:15654276 | A | G | 5 | a0002c0002t0001g0059 a0002c0002t0002g0018 a0002c0002t0002g0287 others(2): Show |
6 | HG02155.hp1 NA18944.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-337-2330T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654276 | |||||||
| chr17:15654401 | C | T | 1 | a0001c0007t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-337-2455G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654401 | |||||||
| chr17:15654591 | C | T | 2 | a0001c0001t0007g0192 a0001c0001t0007g0193 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-337-2645G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654591 | |||||||
| chr17:15654658 | T | C | 8 | a0002c0002t0001g0059 a0002c0002t0002g0018 a0002c0002t0002g0240 others(5): Show |
9 | HG00609.hp1 HG02129.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-337-2712A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654658 | |||||||
| chr17:15654721 | C | A | 1 | a0001c0001t0001g0066 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-337-2775G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654721 | |||||||
| chr17:15654735 | C | T | 1 | a0002c0002t0004g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-337-2789G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654735 | |||||||
| chr17:15654879 | T | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | HG01106.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-337-2933A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654879 | |||||||
| chr17:15654889 | T | C | 100 | a0001c0007t0001g0089 a0001c0007t0002g0254 a0001c0007t0002g0258 others(97): Show |
108 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-337-2943A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654889 | |||||||
| chr17:15654999 | G | GA | 91 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0002c0002t0001g0012 others(88): Show |
98 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-337-3054dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15654999 | |||||||
| chr17:15655032 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-337-3086G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655032 | |||||||
| chr17:15655085 | T | C | 3 | a0003c0004t0003g0011 a0003c0004t0003g0168 a0003c0004t0003g0169 |
4 | HG02145.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-337-3139A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655085 | |||||||
| chr17:15655243 | T | C | 93 | a0001c0007t0001g0089 a0001c0007t0002g0262 a0001c0007t0007g0187 others(90): Show |
100 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-337-3297A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655243 | |||||||
| chr17:15655276 | T | C | 5 | a0001c0010t0006g0323 a0001c0010t0006g0326 a0001c0010t0006g0330 others(2): Show |
5 | HG01934.hp2 HG02735.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-337-3330A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655276 | |||||||
| chr17:15655468 | C | T | 3 | a0003c0014t0005g0112 a0003c0014t0008g0186 a0003c0014t0015g0024 |
3 | HG00738.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-337-3522G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655468 | |||||||
| chr17:15655573 | C | A | 163 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(160): Show |
178 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.-337-3627G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655573 | |||||||
| chr17:15655579 | C | CT | 6 | a0001c0010t0006g0323 a0001c0010t0006g0330 a0005c0012t0016g0023 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-337-3634dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655579 | |||||||
| chr17:15655581 | T | C | 90 | a0002c0002t0001g0012 a0002c0002t0001g0049 a0002c0002t0001g0059 others(87): Show |
97 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.-337-3635A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655581 | |||||||
| chr17:15655628 | T | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-3682A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655628 | |||||||
| chr17:15655667 | C | T | 3 | a0001c0010t0006g0326 a0001c0010t0006g0331 a0005c0021t0002g0253 |
3 | HG01934.hp2 HG02735.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-337-3721G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655667 | |||||||
| chr17:15655699 | C | T | 2 | a0003c0008t0008g0001 a0003c0008t0008g0188 |
5 | HG01884.hp1 HG06807.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-337-3753G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655699 | |||||||
| chr17:15655700 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-3754C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655700 | |||||||
| chr17:15655764 | C | T | 2 | a0002c0002t0002g0014 a0002c0002t0002g0235 |
3 | HG02015.hp1 HG02129.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-337-3818G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655764 | |||||||
| chr17:15655768 | G | T | 54 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0004t0003g0011 others(51): Show |
59 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.-337-3822C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655768 | |||||||
| chr17:15655886 | T | C | 1 | a0002c0006t0001g0180 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-337-3940A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655886 | |||||||
| chr17:15655913 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-337-3967C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655913 | |||||||
| chr17:15655948 | T | C | 1 | a0004c0003t0026g0302 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-337-4002A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15655948 | |||||||
| chr17:15656018 | C | T | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-337-4072G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656018 | |||||||
| chr17:15656026 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0161 |
2 | HG01261.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-337-4080A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656026 | |||||||
| chr17:15656156 | G | T | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-337-4210C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656156 | |||||||
| chr17:15656196 | G | C | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-337-4250C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656196 | |||||||
| chr17:15656268 | A | C | 5 | a0006c0009t0001g0106 a0006c0009t0001g0115 a0006c0009t0002g0213 others(2): Show |
5 | HG01952.hp2 HG01993.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-337-4322T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656268 | |||||||
| chr17:15656361 | T | C | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-337-4415A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656361 | |||||||
| chr17:15656539 | C | T | 2 | a0003c0004t0003g0181 a0003c0004t0003g0182 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-337-4593G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656539 | |||||||
| chr17:15656650 | A | G | 2 | a0001c0007t0002g0254 a0001c0007t0002g0258 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-337-4704T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656650 | |||||||
| chr17:15656660 | C | T | 1 | a0001c0001t0005g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-337-4714G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656660 | |||||||
| chr17:15656681 | C | G | 5 | a0006c0009t0001g0106 a0006c0009t0001g0115 a0006c0009t0002g0213 others(2): Show |
5 | HG01952.hp2 HG01993.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-337-4735G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656681 | |||||||
| chr17:15656691 | G | A | 169 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(166): Show |
184 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-337-4745C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656691 | |||||||
| chr17:15656730 | C | T | 169 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(166): Show |
184 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-337-4784G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656730 | |||||||
| chr17:15656735 | T | G | 2 | a0001c0001t0001g0121 a0001c0001t0002g0318 |
2 | NA18995.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-337-4789A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656735 | |||||||
| chr17:15656805 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-4859G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656805 | |||||||
| chr17:15656966 | A | C | 53 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0004t0003g0011 others(50): Show |
58 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-337-5020T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15656966 | |||||||
| chr17:15657259 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0002g0256 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-337-5313G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15657259 | |||||||
| chr17:15657271 | C | T | 1 | a0003c0017t0003g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-337-5325G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15657271 | |||||||
| chr17:15657406 | A | G | 53 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0004t0003g0011 others(50): Show |
58 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-337-5460T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15657406 | |||||||
| chr17:15657473 | C | T | 3 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0015t0004g0259 |
3 | HG02055.hp1 HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-337-5527G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15657473 | |||||||
| chr17:15657617 | T | C | 2 | a0002c0002t0001g0117 a0002c0002t0021g0189 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-337-5671A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15657617 | |||||||
| chr17:15657913 | T | C | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-5967A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15657913 | |||||||
| chr17:15658354 | T | G | 11 | a0002c0002t0001g0012 a0002c0002t0001g0117 a0002c0002t0001g0170 others(8): Show |
12 | HG02559.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-337-6408A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658354 | |||||||
| chr17:15658395 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-337-6449T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658395 | |||||||
| chr17:15658406 | AT | A | 5 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 others(2): Show |
8 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-337-6461delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658406 | |||||||
| chr17:15658415 | C | T | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-6469G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658415 | |||||||
| chr17:15658456 | C | T | 23 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0025t0004g0313 others(20): Show |
24 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-337-6510G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658456 | |||||||
| chr17:15658479 | C | T | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-6533G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658479 | |||||||
| chr17:15658559 | T | C | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-6613A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658559 | |||||||
| chr17:15658693 | C | G | 2 | a0001c0007t0002g0262 a0001c0007t0007g0187 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-337-6747G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658693 | |||||||
| chr17:15658698 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-6752T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658698 | |||||||
| chr17:15658720 | G | A | 23 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0025t0004g0313 others(20): Show |
24 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-337-6774C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658720 | |||||||
| chr17:15658759 | G | A | 1 | a0002c0002t0002g0274 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-337-6813C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658759 | |||||||
| chr17:15658938 | G | A | 1 | a0001c0007t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-337-6992C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658938 | |||||||
| chr17:15658981 | C | T | 3 | a0002c0006t0001g0175 a0002c0006t0001g0179 a0002c0006t0001g0180 |
3 | HG01168.hp2 HG02698.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-337-7035G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15658981 | |||||||
| chr17:15659006 | T | C | 93 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0098 others(90): Show |
99 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-337-7060A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659006 | |||||||
| chr17:15659105 | G | GA | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-7160dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659105 | |||||||
| chr17:15659126 | T | C | 2 | a0002c0002t0009g0022 a0002c0002t0009g0026 |
2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-337-7180A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659126 | |||||||
| chr17:15659128 | C | G | 13 | a0001c0010t0006g0326 a0001c0010t0006g0331 a0002c0002t0001g0012 others(10): Show |
14 | HG01934.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-337-7182G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659128 | |||||||
| chr17:15659199 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-337-7253T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659199 | |||||||
| chr17:15659257 | C | T | 2 | a0003c0015t0005g0118 a0003c0017t0017g0027 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-337-7311G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659257 | |||||||
| chr17:15659505 | C | A | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-7559G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659505 | |||||||
| chr17:15659696 | G | A | 14 | a0003c0004t0003g0011 a0003c0004t0003g0072 a0003c0004t0003g0073 others(11): Show |
15 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-337-7750C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659696 | |||||||
| chr17:15659737 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-7791A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659737 | |||||||
| chr17:15659846 | G | A | 1 | a0002c0005t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-337-7900C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659846 | |||||||
| chr17:15659902 | C | T | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-7956G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659902 | |||||||
| chr17:15659912 | G | A | 1 | a0001c0007t0012g0006 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-337-7966C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659912 | |||||||
| chr17:15659958 | C | CCAGGG | 13 | a0001c0010t0006g0326 a0001c0010t0006g0331 a0002c0002t0001g0012 others(10): Show |
14 | HG01934.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-337-8017_-337-801 others(9): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15659958 | |||||||
| chr17:15660047 | A | G | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-8101T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660047 | |||||||
| chr17:15660069 | T | C | 1 | a0001c0001t0002g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-337-8123A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660069 | |||||||
| chr17:15660078 | G | A | 13 | a0001c0010t0006g0326 a0001c0010t0006g0331 a0002c0002t0001g0012 others(10): Show |
14 | HG01934.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-337-8132C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660078 | |||||||
| chr17:15660079 | A | G | 169 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(166): Show |
184 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-337-8133T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660079 | |||||||
| chr17:15660211 | A | G | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-8265T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660211 | |||||||
| chr17:15660412 | T | C | 53 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0004t0003g0011 others(50): Show |
58 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-337-8466A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660412 | |||||||
| chr17:15660439 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-8493G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660439 | |||||||
| chr17:15660664 | C | T | 1 | a0005c0012t0027g0328 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-337-8718G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660664 | |||||||
| chr17:15660713 | A | G | 1 | a0004c0003t0004g0298 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-337-8767T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660713 | |||||||
| chr17:15660770 | C | T | 2 | a0001c0007t0002g0262 a0001c0007t0007g0187 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-337-8824G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660770 | |||||||
| chr17:15660790 | T | C | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-337-8844A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660790 | |||||||
| chr17:15660814 | T | C | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-337-8868A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660814 | |||||||
| chr17:15660874 | G | T | 2 | a0003c0004t0003g0075 a0003c0004t0003g0076 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-337-8928C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660874 | |||||||
| chr17:15660897 | C | CA | 13 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0061 others(10): Show |
13 | HG00408.hp1 HG01070.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-337-8952dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660897 | |||||||
| chr17:15660897 | CA | C | 52 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(49): Show |
56 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-337-8952delT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660897 | |||||||
| chr17:15660897 | CAA | C | 114 | a0001c0001t0002g0275 a0001c0001t0002g0314 a0001c0007t0001g0089 others(111): Show |
124 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-337-8953_-337-895 others(6): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660897 | |||||||
| chr17:15660897 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-337-8961_-337-895 others(14): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660897 | |||||||
| chr17:15660957 | A | T | 2 | a0001c0007t0002g0262 a0001c0007t0007g0187 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-337-9011T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15660957 | |||||||
| chr17:15661000 | C | T | 1 | a0002c0005t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-337-9054G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661000 | |||||||
| chr17:15661020 | C | A | 1 | a0001c0001t0002g0264 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-337-9074G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661020 | |||||||
| chr17:15661041 | T | C | 3 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0015t0004g0259 |
3 | HG02055.hp1 HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-337-9095A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661041 | |||||||
| chr17:15661232 | A | G | 169 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(166): Show |
184 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-337-9286T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661232 | |||||||
| chr17:15661299 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-337-9353C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661299 | |||||||
| chr17:15661331 | G | C | 1 | a0002c0002t0002g0263 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-337-9385C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661331 | |||||||
| chr17:15661496 | G | A | 6 | a0001c0010t0006g0323 a0001c0010t0006g0330 a0005c0012t0016g0023 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-337-9550C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661496 | |||||||
| chr17:15661622 | T | C | 23 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0025t0004g0313 others(20): Show |
24 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-337-9676A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661622 | |||||||
| chr17:15661654 | T | C | 1 | a0002c0002t0002g0220 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-337-9708A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661654 | |||||||
| chr17:15661665 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-337-9719C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661665 | |||||||
| chr17:15661841 | C | CT | 6 | a0001c0010t0006g0323 a0001c0010t0006g0330 a0005c0012t0016g0023 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-337-9896dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661841 | |||||||
| chr17:15661944 | C | T | 10 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0012g0006 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-337-9998G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15661944 | |||||||
| chr17:15662155 | A | G | 5 | a0003c0008t0008g0001 a0003c0008t0008g0188 a0003c0014t0005g0112 others(2): Show |
8 | HG00738.hp2 HG01884.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-337-10209T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15662155 | |||||||
| chr17:15662227 | C | T | 81 | a0001c0001t0002g0275 a0002c0002t0001g0049 a0002c0002t0001g0059 others(78): Show |
87 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-337-10281G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15662227 | |||||||
| chr17:15662292 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-337-10346A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15662292 | |||||||
| chr17:15662638 | T | C | 31 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0008t0008g0001 others(28): Show |
35 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-337-10692A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15662638 | |||||||
| chr17:15662915 | G | A | 24 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0003c0015t0001g0105 others(21): Show |
25 | HG00597.hp2 HG00621.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.-337-10969C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15662915 | |||||||
| chr17:15663143 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
11 | HG01109.hp2 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-337-11197T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663143 | |||||||
| chr17:15663169 | C | T | 1 | a0003c0015t0001g0105 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-337-11223G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663169 | |||||||
| chr17:15663265 | T | G | 81 | a0001c0001t0002g0275 a0002c0002t0001g0049 a0002c0002t0001g0059 others(78): Show |
87 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-337-11319A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663265 | |||||||
| chr17:15663387 | A | G | 1 | a0001c0007t0007g0187 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-337-11441T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663387 | |||||||
| chr17:15663684 | C | G | 14 | a0001c0001t0001g0177 a0001c0010t0006g0326 a0001c0010t0006g0331 others(11): Show |
15 | HG01071.hp2 HG01934.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-337-11738G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663684 | |||||||
| chr17:15663728 | C | T | 81 | a0001c0001t0002g0275 a0002c0002t0001g0049 a0002c0002t0001g0059 others(78): Show |
87 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-337-11782G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663728 | |||||||
| chr17:15663817 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-337-11871G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663817 | |||||||
| chr17:15663830 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-337-11884G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663830 | |||||||
| chr17:15663882 | A | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
12 | HG01109.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-337-11936T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663882 | |||||||
| chr17:15663907 | T | C | 84 | a0001c0001t0002g0275 a0001c0007t0001g0089 a0001c0007t0002g0262 others(81): Show |
90 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-337-11961A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663907 | |||||||
| chr17:15663947 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-337-12001C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663947 | |||||||
| chr17:15663957 | C | G | 1 | a0003c0004t0003g0168 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-337-12011G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15663957 | |||||||
| chr17:15664186 | G | A | 13 | a0001c0010t0006g0326 a0001c0010t0006g0331 a0002c0002t0001g0012 others(10): Show |
14 | HG01934.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-337-12240C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664186 | |||||||
| chr17:15664192 | A | G | 88 | a0001c0001t0002g0275 a0001c0007t0012g0006 a0001c0010t0006g0323 others(85): Show |
95 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-337-12246T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664192 | |||||||
| chr17:15664355 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
15 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-337-12409A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664355 | |||||||
| chr17:15664464 | G | A | 23 | a0001c0011t0014g0332 a0001c0011t0014g0333 a0002c0002t0002g0321 others(20): Show |
24 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-337-12518C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664464 | |||||||
| chr17:15664516 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-337-12570C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664516 | |||||||
| chr17:15664565 | G | A | 2 | a0002c0002t0001g0119 a0002c0002t0002g0260 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-338+12611C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664565 | |||||||
| chr17:15664719 | T | C | 25 | a0001c0001t0002g0314 a0001c0011t0014g0332 a0001c0011t0014g0333 others(22): Show |
26 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.-338+12457A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664719 | |||||||
| chr17:15664756 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-338+12420G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664756 | |||||||
| chr17:15664757 | G | A | 5 | a0001c0001t0002g0243 a0001c0001t0006g0324 a0001c0001t0006g0325 others(2): Show |
6 | HG01934.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-338+12419C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664757 | |||||||
| chr17:15664922 | C | T | 1 | a0002c0002t0001g0170 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-338+12254G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664922 | |||||||
| chr17:15664956 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-338+12220G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664956 | |||||||
| chr17:15664974 | G | T | 26 | a0001c0001t0002g0314 a0001c0001t0002g0320 a0001c0011t0014g0332 others(23): Show |
27 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.-338+12202C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15664974 | |||||||
| chr17:15665000 | C | G | 3 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0003c0015t0004g0259 |
3 | HG02055.hp1 HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-338+12176G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665000 | |||||||
| chr17:15665011 | A | G | 4 | a0001c0001t0002g0021 a0001c0001t0002g0315 a0001c0001t0002g0316 others(1): Show |
5 | NA18943.hp1 NA18997.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.-338+12165T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665011 | |||||||
| chr17:15665026 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(6): Show |
10 | HG01070.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-338+12150G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665026 | |||||||
| chr17:15665031 | C | CA | 8 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0001g0100 others(5): Show |
8 | HG00423.hp1 HG00621.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.-338+12144dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665031 | |||||||
| chr17:15665031 | CA | C | 25 | a0001c0001t0001g0038 a0001c0001t0001g0081 a0001c0001t0001g0083 others(22): Show |
25 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-338+12144delT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665031 | |||||||
| chr17:15665031 | CAA | C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(160): Show |
179 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-338+12143_-338+12 others(8): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665031 | |||||||
| chr17:15665031 | CAAA | C | 12 | a0001c0001t0001g0164 a0001c0001t0001g0173 a0001c0024t0007g0190 others(9): Show |
14 | HG00738.hp1 HG01070.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-338+12142_-338+12 others(9): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665031 | |||||||
| chr17:15665238 | C | T | 1 | a0002c0006t0001g0141 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-338+11938G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665238 | |||||||
| chr17:15665241 | A | G | 25 | a0001c0001t0001g0167 a0001c0001t0001g0173 a0001c0007t0001g0089 others(22): Show |
27 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-338+11935T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665241 | |||||||
| chr17:15665244 | G | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0010c0023t0001g0054 |
3 | HG00323.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-338+11932C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665244 | |||||||
| chr17:15665250 | T | C | 45 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0107 others(42): Show |
45 | HG00323.hp2 HG00735.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.-338+11926A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665250 | |||||||
| chr17:15665251 | G | A | 11 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0002g0203 others(8): Show |
11 | HG00735.hp2 HG01074.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.-338+11925C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665251 | |||||||
| chr17:15665278 | T | C | 7 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0007g0187 others(4): Show |
10 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-338+11898A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665278 | |||||||
| chr17:15665280 | C | A | 7 | a0001c0007t0002g0254 a0001c0007t0002g0258 a0001c0007t0007g0187 others(4): Show |
10 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-338+11896G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665280 | |||||||
| chr17:15665294 | C | T | 14 | a0001c0001t0001g0173 a0002c0002t0001g0117 a0002c0002t0009g0022 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-338+11882G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665294 | |||||||
| chr17:15665305 | C | A | 26 | a0001c0001t0001g0167 a0001c0001t0001g0173 a0001c0007t0012g0006 others(23): Show |
29 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.-338+11871G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665305 | |||||||
| chr17:15665305 | C | T | 1 | a0002c0002t0007g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-338+11871G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665305 | |||||||
| chr17:15665310 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0030 others(58): Show |
65 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.-338+11866G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665310 | |||||||
| chr17:15665316 | T | C | 5 | a0002c0002t0009g0022 a0002c0002t0009g0026 a0003c0014t0015g0024 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-338+11860A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665316 | |||||||
| chr17:15665318 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0185 a0001c0001t0002g0314 |
3 | NA18962.hp1 NA18999.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-338+11858C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665318 | |||||||
| chr17:15665324 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-338+11852G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665324 | |||||||
| chr17:15665326 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0074 others(83): Show |
96 | HG00323.hp2 HG00609.hp1 HG01109.hp2 others(93): Show |
intron_variant | MODIFIER | c.-338+11850T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665326 | |||||||
| chr17:15665337 | A | G | 3 | a0001c0001t0002g0281 a0001c0024t0007g0190 a0003c0015t0001g0105 |
3 | HG02083.hp2 HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-338+11839T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665337 | |||||||
| chr17:15665366 | G | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
262 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-338+11810C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665366 | |||||||
| chr17:15665370 | A | G | 1 | a0001c0001t0002g0314 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-338+11806T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665370 | |||||||
| chr17:15665381 | T | C | 7 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0052 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-338+11795A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665381 | |||||||
| chr17:15665385 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-338+11791A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665385 | |||||||
| chr17:15665402 | A | G | 23 | a0001c0001t0001g0129 a0001c0001t0002g0198 a0001c0001t0002g0211 others(20): Show |
27 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-338+11774T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665402 | |||||||
| chr17:15665426 | G | A | 1 | a0002c0002t0001g0166 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-338+11750C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665426 | |||||||
| chr17:15665434 | G | A | 1 | a0002c0002t0002g0291 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-338+11742C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665434 | |||||||
| chr17:15665550 | T | C | 4 | a0004c0003t0011g0299 a0004c0003t0011g0300 a0004c0003t0011g0301 others(1): Show |
4 | NA18960.hp1 NA18989.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-338+11626A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665550 | |||||||
| chr17:15665552 | A | G | 4 | a0004c0003t0011g0299 a0004c0003t0011g0300 a0004c0003t0011g0301 others(1): Show |
4 | NA18960.hp1 NA18989.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-338+11624T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665552 | |||||||
| chr17:15665563 | A | G | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-338+11613T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665563 | |||||||
| chr17:15665570 | T | A | 3 | a0001c0007t0007g0187 a0003c0008t0008g0001 a0003c0008t0008g0188 |
6 | HG01884.hp1 HG02922.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-338+11606A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665570 | |||||||
| chr17:15665593 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-338+11583C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665593 | |||||||
| chr17:15665601 | A | G | 11 | a0001c0001t0001g0091 a0001c0007t0007g0187 a0002c0002t0002g0226 others(8): Show |
14 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-338+11575T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665601 | |||||||
| chr17:15665624 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0091 a0001c0001t0002g0252 others(2): Show |
5 | HG02027.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-338+11552T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665624 | |||||||
| chr17:15665711 | A | ACTT | 11 | a0001c0001t0002g0199 a0001c0001t0007g0192 a0001c0001t0007g0193 others(8): Show |
14 | HG00408.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-338+11462_-338+11 others(9): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665711 | |||||||
| chr17:15665794 | C | T | 281 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(278): Show |
303 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(300): Show |
intron_variant | MODIFIER | c.-338+11382G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665794 | |||||||
| chr17:15665801 | C | A | 1 | a0002c0002t0001g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-338+11375G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665801 | |||||||
| chr17:15665883 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
6 | HG00609.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-338+11293A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665883 | |||||||
| chr17:15665945 | T | TG | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+11230dupC | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15665945 | |||||||
| chr17:15666047 | A | C | 1 | a0004c0003t0004g0297 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-338+11129T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666047 | |||||||
| chr17:15666094 | A | G | 1 | a0002c0002t0002g0263 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-338+11082T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666094 | |||||||
| chr17:15666260 | T | C | 1 | a0009c0016t0003g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-338+10916A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666260 | |||||||
| chr17:15666372 | G | T | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+10804C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666372 | |||||||
| chr17:15666405 | T | C | 3 | a0002c0002t0001g0117 a0003c0015t0005g0118 a0003c0017t0017g0027 |
3 | HG02970.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-338+10771A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666405 | |||||||
| chr17:15666594 | C | T | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+10582G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666594 | |||||||
| chr17:15666620 | A | T | 3 | a0001c0001t0001g0167 a0003c0004t0003g0181 a0003c0004t0003g0182 |
3 | HG01109.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-338+10556T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666620 | |||||||
| chr17:15666661 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0120 others(46): Show |
52 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.-338+10515T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666661 | |||||||
| chr17:15666724 | T | C | 3 | a0002c0002t0001g0117 a0003c0015t0005g0118 a0003c0017t0017g0027 |
3 | HG02970.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-338+10452A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666724 | |||||||
| chr17:15666883 | G | C | 5 | a0003c0004t0003g0072 a0003c0004t0003g0073 a0003c0004t0003g0127 others(2): Show |
5 | HG02109.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-338+10293C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666883 | |||||||
| chr17:15666975 | G | A | 1 | a0002c0002t0001g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-338+10201C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666975 | |||||||
| chr17:15666981 | C | T | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(204): Show |
221 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.-338+10195G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15666981 | |||||||
| chr17:15667258 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-338+9918A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667258 | |||||||
| chr17:15667416 | A | T | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-338+9760T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667416 | |||||||
| chr17:15667457 | T | C | 1 | a0001c0001t0006g0327 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-338+9719A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667457 | |||||||
| chr17:15667470 | C | T | 14 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 others(11): Show |
14 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.-338+9706G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667470 | |||||||
| chr17:15667559 | T | C | 1 | a0001c0001t0006g0327 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-338+9617A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667559 | |||||||
| chr17:15667660 | T | C | 10 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0002c0002t0001g0111 others(7): Show |
10 | HG00642.hp2 HG00738.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-338+9516A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667660 | |||||||
| chr17:15667730 | A | G | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+9446T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667730 | |||||||
| chr17:15667746 | T | G | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+9430A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667746 | |||||||
| chr17:15667828 | C | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(70): Show |
80 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.-338+9348G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667828 | |||||||
| chr17:15667845 | T | C | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+9331A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667845 | |||||||
| chr17:15667930 | C | T | 7 | a0001c0001t0002g0222 a0001c0001t0004g0224 a0001c0001t0010g0013 others(4): Show |
8 | HG01192.hp1 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-338+9246G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15667930 | |||||||
| chr17:15668289 | A | G | 1 | a0004c0003t0004g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-338+8887T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15668289 | |||||||
| chr17:15668555 | T | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
313 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.-338+8621A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15668555 | |||||||
| chr17:15668627 | GCTTTTGC others(13): Show |
G | 11 | a0001c0001t0001g0173 a0002c0002t0001g0012 a0002c0002t0001g0170 others(8): Show |
13 | HG02145.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-338+8529_-338+854 others(24): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15668627 | |||||||
| chr17:15668677 | A | G | 9 | a0001c0001t0002g0281 a0002c0002t0002g0216 a0002c0002t0002g0217 others(6): Show |
9 | HG00735.hp2 HG01255.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.-338+8499T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15668677 | |||||||
| chr17:15668784 | G | A | 1 | a0001c0010t0006g0331 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-338+8392C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15668784 | |||||||
| chr17:15668833 | A | G | 285 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(282): Show |
310 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(307): Show |
intron_variant | MODIFIER | c.-338+8343T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15668833 | |||||||
| chr17:15668984 | A | T | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+8192T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15668984 | |||||||
| chr17:15669084 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
7 | HG02615.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-338+8092T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669084 | |||||||
| chr17:15669171 | C | T | 3 | a0001c0007t0007g0187 a0003c0008t0008g0001 a0003c0008t0008g0188 |
6 | HG01884.hp1 HG02922.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-338+8005G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669171 | |||||||
| chr17:15669233 | C | T | 1 | a0002c0002t0002g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-338+7943G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669233 | |||||||
| chr17:15669243 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(277): Show |
305 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(302): Show |
intron_variant | MODIFIER | c.-338+7933T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669243 | |||||||
| chr17:15669264 | C | G | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+7912G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669264 | |||||||
| chr17:15669302 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-338+7874A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669302 | |||||||
| chr17:15669339 | G | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
309 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.-338+7837C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669339 | |||||||
| chr17:15669563 | T | G | 104 | a0001c0001t0002g0211 a0001c0001t0002g0222 a0001c0001t0002g0228 others(101): Show |
111 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.-338+7613A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669563 | |||||||
| chr17:15669578 | G | GTA | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+7596_-338+759 others(6): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669578 | |||||||
| chr17:15669580 | A | G | 14 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(11): Show |
14 | HG00438.hp2 HG00621.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-338+7596T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669580 | |||||||
| chr17:15669581 | T | C | 1 | a0001c0007t0012g0006 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-338+7595A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669581 | |||||||
| chr17:15669655 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-338+7521C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669655 | |||||||
| chr17:15669684 | C | T | 1 | a0001c0007t0012g0006 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-338+7492G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669684 | |||||||
| chr17:15669689 | G | A | 5 | a0002c0002t0009g0022 a0002c0002t0009g0026 a0003c0014t0015g0024 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-338+7487C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669689 | |||||||
| chr17:15669802 | G | A | 1 | a0001c0024t0007g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-338+7374C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669802 | |||||||
| chr17:15669802 | G | C | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
297 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(294): Show |
intron_variant | MODIFIER | c.-338+7374C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669802 | |||||||
| chr17:15669852 | G | A | 2 | a0003c0015t0005g0118 a0003c0017t0017g0027 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-338+7324C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15669852 | |||||||
| chr17:15670191 | G | C | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+6985C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670191 | |||||||
| chr17:15670242 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-338+6934G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670242 | |||||||
| chr17:15670462 | A | G | 2 | a0006c0009t0002g0213 a0006c0009t0002g0214 |
2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-338+6714T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670462 | |||||||
| chr17:15670519 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-338+6657G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670519 | |||||||
| chr17:15670554 | C | A | 5 | a0002c0002t0009g0022 a0002c0002t0009g0026 a0003c0014t0015g0024 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-338+6622G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670554 | |||||||
| chr17:15670696 | G | GT | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+6479dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670696 | |||||||
| chr17:15670722 | T | C | 14 | a0001c0001t0002g0021 a0001c0001t0002g0314 a0001c0001t0002g0315 others(11): Show |
16 | HG00621.hp2 HG02080.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.-338+6454A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670722 | |||||||
| chr17:15670790 | C | T | 2 | a0001c0001t0007g0192 a0001c0001t0007g0193 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-338+6386G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670790 | |||||||
| chr17:15670803 | A | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
82 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.-338+6373T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670803 | |||||||
| chr17:15670982 | G | A | 1 | a0002c0002t0002g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-338+6194C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670982 | |||||||
| chr17:15670987 | GT | G | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+6188delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15670987 | |||||||
| chr17:15671031 | G | T | 1 | a0001c0007t0002g0254 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-338+6145C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671031 | |||||||
| chr17:15671315 | G | GTATA | 285 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(282): Show |
310 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(307): Show |
intron_variant | MODIFIER | c.-338+5860_-338+586 others(8): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671315 | |||||||
| chr17:15671366 | T | C | 1 | a0010c0023t0001g0054 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-338+5810A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671366 | |||||||
| chr17:15671425 | G | T | 1 | a0002c0002t0002g0280 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-338+5751C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671425 | |||||||
| chr17:15671545 | A | G | 1 | a0001c0024t0007g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-338+5631T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671545 | |||||||
| chr17:15671549 | A | G | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+5627T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671549 | |||||||
| chr17:15671611 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-338+5565T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671611 | |||||||
| chr17:15671612 | T | C | 3 | a0002c0002t0001g0117 a0003c0015t0005g0118 a0003c0017t0017g0027 |
3 | HG02970.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-338+5564A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671612 | |||||||
| chr17:15671684 | C | G | 1 | a0003c0014t0008g0186 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-338+5492G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671684 | |||||||
| chr17:15671971 | TA | T | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+5204delT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671971 | |||||||
| chr17:15671984 | T | C | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+5192A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15671984 | |||||||
| chr17:15672019 | T | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0304 a0001c0001t0002g0305 others(28): Show |
33 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-338+5157A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672019 | |||||||
| chr17:15672134 | T | C | 1 | a0002c0002t0002g0244 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-338+5042A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672134 | |||||||
| chr17:15672683 | T | C | 1 | a0002c0002t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-338+4493A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672683 | |||||||
| chr17:15672689 | C | T | 8 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
8 | HG02155.hp2 NA18946.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.-338+4487G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672689 | |||||||
| chr17:15672694 | C | T | 2 | a0003c0015t0005g0118 a0003c0017t0017g0027 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-338+4482G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672694 | |||||||
| chr17:15672698 | A | G | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0074 others(48): Show |
54 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.-338+4478T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672698 | |||||||
| chr17:15672753 | T | A | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+4423A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672753 | |||||||
| chr17:15672786 | C | T | 1 | a0005c0021t0002g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-338+4390G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672786 | |||||||
| chr17:15672968 | T | C | 2 | a0003c0004t0003g0181 a0003c0004t0003g0182 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-338+4208A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15672968 | |||||||
| chr17:15673121 | C | A | 1 | a0002c0002t0001g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-338+4055G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15673121 | |||||||
| chr17:15673158 | T | C | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+4018A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15673158 | |||||||
| chr17:15673229 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-338+3947G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15673229 | |||||||
| chr17:15673278 | T | C | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0074 others(48): Show |
54 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.-338+3898A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15673278 | |||||||
| chr17:15673293 | G | A | 14 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(11): Show |
14 | HG00438.hp2 HG00621.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.-338+3883C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15673293 | |||||||
| chr17:15673765 | C | A | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+3411G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15673765 | |||||||
| chr17:15673866 | T | A | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+3310A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15673866 | |||||||
| chr17:15673868 | A | G | 10 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0002c0002t0001g0111 others(7): Show |
10 | HG00642.hp2 HG00738.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-338+3308T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15673868 | |||||||
| chr17:15674223 | AGCCGGGC others(47): Show |
A | 1 | a0002c0002t0002g0268 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-338+2899_-338+295 others(58): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674223 | |||||||
| chr17:15674315 | A | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
94 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.-338+2861T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674315 | |||||||
| chr17:15674646 | T | C | 8 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(5): Show |
11 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-338+2530A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674646 | |||||||
| chr17:15674655 | T | C | 10 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(7): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-338+2521A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674655 | |||||||
| chr17:15674671 | C | T | 1 | a0002c0005t0002g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-338+2505G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674671 | |||||||
| chr17:15674686 | T | C | 10 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(7): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-338+2490A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674686 | |||||||
| chr17:15674809 | A | G | 1 | a0002c0002t0007g0191 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-338+2367T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674809 | |||||||
| chr17:15674824 | G | A | 3 | a0002c0002t0001g0117 a0003c0015t0005g0118 a0003c0017t0017g0027 |
3 | HG02970.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-338+2352C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674824 | |||||||
| chr17:15674829 | G | C | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-338+2347C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674829 | |||||||
| chr17:15674860 | A | G | 4 | a0001c0001t0001g0033 a0001c0007t0012g0006 a0002c0002t0007g0191 others(1): Show |
5 | HG02027.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-338+2316T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674860 | |||||||
| chr17:15674995 | T | C | 5 | a0001c0001t0002g0248 a0002c0002t0002g0017 a0002c0002t0002g0246 others(2): Show |
6 | HG02056.hp2 HG02083.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.-338+2181A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15674995 | |||||||
| chr17:15675121 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(113): Show |
129 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.-338+2055G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675121 | |||||||
| chr17:15675173 | A | T | 1 | a0002c0002t0001g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-338+2003T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675173 | |||||||
| chr17:15675349 | T | A | 1 | a0002c0002t0004g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-338+1827A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675349 | |||||||
| chr17:15675534 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-338+1642A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675534 | |||||||
| chr17:15675538 | G | A | 286 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(283): Show |
309 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.-338+1638C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675538 | |||||||
| chr17:15675669 | C | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-338+1507G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675669 | |||||||
| chr17:15675683 | G | A | 5 | a0001c0007t0007g0187 a0002c0002t0021g0189 a0003c0008t0008g0001 others(2): Show |
8 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-338+1493C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675683 | |||||||
| chr17:15675708 | T | C | 1 | a0001c0001t0002g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-338+1468A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675708 | |||||||
| chr17:15675745 | G | A | 5 | a0001c0007t0007g0187 a0002c0002t0021g0189 a0003c0008t0008g0001 others(2): Show |
8 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-338+1431C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675745 | |||||||
| chr17:15675760 | C | CATACGTA others(77): Show |
1 | a0001c0001t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-338+1415_-338+141 others(88): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675760 | |||||||
| chr17:15675784 | C | T | 2 | a0003c0015t0005g0118 a0003c0017t0017g0027 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-338+1392G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675784 | |||||||
| chr17:15675855 | C | CAT | 34 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0084 others(31): Show |
36 | HG00544.hp2 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-338+1319_-338+132 others(6): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675855 | |||||||
| chr17:15675900 | G | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01106.hp2 HG01243.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-338+1276C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675900 | |||||||
| chr17:15675991 | A | G | 5 | a0001c0007t0007g0187 a0002c0002t0021g0189 a0003c0008t0008g0001 others(2): Show |
8 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-338+1185T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15675991 | |||||||
| chr17:15676078 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-338+1098T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676078 | |||||||
| chr17:15676134 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
7 | HG02615.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-338+1042T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676134 | |||||||
| chr17:15676160 | T | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0120 others(46): Show |
52 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.-338+1016A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676160 | |||||||
| chr17:15676167 | T | C | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-338+1009A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676167 | |||||||
| chr17:15676228 | C | T | 1 | a0004c0003t0004g0303 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-338+948G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676228 | |||||||
| chr17:15676243 | C | T | 5 | a0001c0007t0007g0187 a0002c0002t0021g0189 a0003c0008t0008g0001 others(2): Show |
8 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-338+933G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676243 | |||||||
| chr17:15676279 | G | A | 1 | a0002c0002t0001g0166 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-338+897C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676279 | |||||||
| chr17:15676294 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-338+882A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676294 | |||||||
| chr17:15676431 | CT | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0074 others(41): Show |
48 | HG00544.hp2 HG00741.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.-338+744delA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676431 | |||||||
| chr17:15676431 | CTT | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(237): Show |
259 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.-338+743_-338+744d others(4): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676431 | |||||||
| chr17:15676503 | C | T | 148 | a0001c0001t0002g0021 a0001c0001t0002g0198 a0001c0001t0002g0199 others(145): Show |
157 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-338+673G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676503 | |||||||
| chr17:15676508 | C | T | 1 | a0002c0002t0002g0279 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-338+668G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676508 | |||||||
| chr17:15676536 | C | T | 1 | a0002c0002t0002g0276 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-338+640G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676536 | |||||||
| chr17:15676580 | T | C | 281 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(278): Show |
301 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.-338+596A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676580 | |||||||
| chr17:15676678 | G | A | 5 | a0001c0007t0007g0187 a0002c0002t0021g0189 a0003c0008t0008g0001 others(2): Show |
8 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-338+498C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676678 | |||||||
| chr17:15676726 | C | T | 62 | a0001c0001t0002g0222 a0001c0001t0002g0228 a0001c0001t0002g0233 others(59): Show |
67 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-338+450G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676726 | |||||||
| chr17:15676765 | C | T | 1 | a0001c0007t0012g0006 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-338+411G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676765 | |||||||
| chr17:15676815 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(79): Show |
89 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.-338+361A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676815 | |||||||
| chr17:15676844 | T | G | 1 | a0001c0001t0002g0320 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-338+332A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676844 | |||||||
| chr17:15676918 | T | C | 1 | a0003c0017t0003g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-338+258A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15676918 | |||||||
| chr17:15677060 | T | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(85): Show |
95 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.-338+116A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15677060 | |||||||
| chr17:15677112 | G | C | 10 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(7): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-338+64C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15677112 | |||||||
| chr17:15677169 | CACTT | C | 4 | a0001c0010t0006g0323 a0001c0010t0006g0330 a0005c0012t0027g0328 others(1): Show |
4 | HG01884.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-338+3_-338+6delAA others(2): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 6/11 | chr17 | 15677169 | |||||||
| chr17:15677473 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-443+102G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 5/11 | chr17 | 15677473 | |||||||
| chr17:15677838 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-589-117T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15677838 | |||||||
| chr17:15678059 | T | C | 4 | a0002c0002t0002g0274 a0002c0002t0021g0189 a0003c0008t0008g0001 others(1): Show |
7 | HG01256.hp1 HG01884.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-589-338A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678059 | |||||||
| chr17:15678092 | G | A | 2 | a0003c0015t0005g0118 a0003c0017t0017g0027 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-589-371C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678092 | |||||||
| chr17:15678099 | G | A | 8 | a0001c0001t0001g0173 a0002c0002t0001g0012 a0002c0002t0001g0170 others(5): Show |
10 | HG02145.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-589-378C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678099 | |||||||
| chr17:15678167 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0084 others(26): Show |
31 | HG00544.hp2 HG00741.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.-589-446G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678167 | |||||||
| chr17:15678218 | C | CA | 24 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0173 others(21): Show |
24 | HG00642.hp2 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-589-498dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678218 | |||||||
| chr17:15678275 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-589-554A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678275 | |||||||
| chr17:15678338 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-589-617G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678338 | |||||||
| chr17:15678346 | C | T | 5 | a0001c0007t0007g0187 a0002c0002t0021g0189 a0003c0008t0008g0001 others(2): Show |
8 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-589-625G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678346 | |||||||
| chr17:15678374 | C | T | 1 | a0004c0003t0001g0104 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-589-653G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678374 | |||||||
| chr17:15678677 | A | G | 4 | a0004c0003t0011g0299 a0004c0003t0011g0300 a0004c0003t0011g0301 others(1): Show |
4 | NA18960.hp1 NA18989.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-589-956T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678677 | |||||||
| chr17:15678690 | C | T | 1 | a0001c0010t0006g0323 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-589-969G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678690 | |||||||
| chr17:15678704 | G | T | 10 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(7): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-589-983C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678704 | |||||||
| chr17:15678855 | C | T | 1 | a0004c0003t0004g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-589-1134G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678855 | |||||||
| chr17:15678875 | CTCCTT | C | 146 | a0001c0001t0002g0021 a0001c0001t0002g0198 a0001c0001t0002g0199 others(143): Show |
155 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-589-1159_-589-115 others(9): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678875 | |||||||
| chr17:15678878 | C | CT | 28 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0121 others(25): Show |
32 | HG00642.hp2 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-589-1158dupA | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678878 | |||||||
| chr17:15678878 | C | CTT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(79): Show |
88 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.-589-1159_-589-115 others(6): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678878 | |||||||
| chr17:15678878 | C | CTTT | 24 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0083 others(21): Show |
26 | HG00544.hp2 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-589-1160_-589-115 others(7): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678878 | |||||||
| chr17:15678940 | C | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-589-1219G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678940 | |||||||
| chr17:15678945 | G | C | 1 | a0001c0010t0006g0331 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-589-1224C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15678945 | |||||||
| chr17:15679051 | G | A | 2 | a0002c0002t0002g0019 a0002c0002t0002g0291 |
3 | HG02129.hp1 NA18942.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-589-1330C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679051 | |||||||
| chr17:15679177 | C | G | 2 | a0003c0004t0003g0072 a0003c0004t0003g0073 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-589-1456G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679177 | |||||||
| chr17:15679303 | T | A | 2 | a0003c0015t0005g0118 a0003c0017t0017g0027 |
2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-590+1562A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679303 | |||||||
| chr17:15679319 | T | C | 1 | a0001c0001t0001g0007 | 2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-590+1546A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679319 | |||||||
| chr17:15679410 | A | ACGTG | 2 | a0001c0007t0001g0089 a0007c0013t0001g0009 |
3 | HG02257.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-590+1451_-590+145 others(8): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679410 | |||||||
| chr17:15679411 | C | T | 1 | a0002c0002t0002g0276 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-590+1454G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679411 | |||||||
| chr17:15679412 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-590+1453C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679412 | |||||||
| chr17:15679487 | G | GC | 9 | a0001c0001t0001g0173 a0002c0002t0001g0012 a0002c0002t0001g0170 others(6): Show |
11 | HG02145.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-590+1377dupG | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679487 | |||||||
| chr17:15679537 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-590+1328A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679537 | |||||||
| chr17:15679708 | C | T | 1 | a0004c0003t0004g0298 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-590+1157G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679708 | |||||||
| chr17:15679733 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0084 others(23): Show |
28 | HG00544.hp2 HG00741.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-590+1132G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679733 | |||||||
| chr17:15679762 | C | T | 1 | a0004c0003t0004g0297 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-590+1103G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679762 | |||||||
| chr17:15679798 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-590+1067C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679798 | |||||||
| chr17:15679806 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
126 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(123): Show |
intron_variant | MODIFIER | c.-590+1059C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679806 | |||||||
| chr17:15679853 | A | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(134): Show |
150 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(147): Show |
intron_variant | MODIFIER | c.-590+1012T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679853 | |||||||
| chr17:15679885 | T | A | 5 | a0001c0007t0007g0187 a0002c0002t0021g0189 a0003c0008t0008g0001 others(2): Show |
8 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-590+980A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679885 | |||||||
| chr17:15679915 | C | T | 1 | a0002c0002t0001g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-590+950G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679915 | |||||||
| chr17:15679920 | G | C | 5 | a0002c0002t0009g0022 a0002c0002t0009g0026 a0003c0014t0015g0024 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-590+945C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679920 | |||||||
| chr17:15679924 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(8): Show |
12 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-590+941C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679924 | |||||||
| chr17:15679936 | C | CA | 141 | a0001c0001t0002g0021 a0001c0001t0002g0198 a0001c0001t0002g0199 others(138): Show |
150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-590+928dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679936 | |||||||
| chr17:15679936 | CA | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(117): Show |
130 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(127): Show |
intron_variant | MODIFIER | c.-590+928delT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679936 | |||||||
| chr17:15679952 | G | A | 1 | a0001c0001t0002g0275 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-590+913C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679952 | |||||||
| chr17:15679953 | A | G | 1 | a0001c0001t0002g0275 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-590+912T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15679953 | |||||||
| chr17:15680042 | T | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(124): Show |
137 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(134): Show |
intron_variant | MODIFIER | c.-590+823A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680042 | |||||||
| chr17:15680201 | T | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
126 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(123): Show |
intron_variant | MODIFIER | c.-590+664A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680201 | |||||||
| chr17:15680232 | T | A | 4 | a0001c0007t0007g0187 a0002c0002t0021g0189 a0003c0008t0008g0001 others(1): Show |
7 | HG01884.hp1 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-590+633A>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680232 | |||||||
| chr17:15680241 | C | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(85): Show |
95 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.-590+624G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680241 | |||||||
| chr17:15680328 | A | AGGCCCTT others(9): Show |
127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(124): Show |
137 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(134): Show |
intron_variant | MODIFIER | c.-590+521_-590+536d others(18): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680328 | |||||||
| chr17:15680443 | C | T | 15 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 others(12): Show |
15 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.-590+422G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680443 | |||||||
| chr17:15680449 | G | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(67): Show |
77 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.-590+416C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680449 | |||||||
| chr17:15680515 | T | C | 1 | a0002c0002t0002g0267 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-590+350A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680515 | |||||||
| chr17:15680565 | A | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-590+300T>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680565 | |||||||
| chr17:15680609 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-590+256C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680609 | |||||||
| chr17:15680663 | G | T | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(134): Show |
150 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(147): Show |
intron_variant | MODIFIER | c.-590+202C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680663 | |||||||
| chr17:15680748 | A | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0084 others(7): Show |
11 | HG00544.hp2 HG02015.hp2 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.-590+117T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680748 | |||||||
| chr17:15680757 | G | GA | 10 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(7): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-590+107dupT | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680757 | |||||||
| chr17:15680790 | T | TAAGAATG others(43): Show |
1 | a0002c0002t0002g0268 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-590+74_-590+75ins others(50): Show |
TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680790 | |||||||
| chr17:15680792 | T | C | 1 | a0002c0002t0002g0268 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-590+73A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680792 | |||||||
| chr17:15680795 | G | A | 1 | a0002c0002t0002g0268 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-590+70C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 4/11 | chr17 | 15680795 | |||||||
| chr17:15680972 | A | T | 1 | a0004c0003t0004g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-678-19T>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15680972 | |||||||
| chr17:15681091 | G | A | 2 | a0001c0001t0002g0269 a0001c0001t0002g0270 |
2 | NA18946.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-678-138C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681091 | |||||||
| chr17:15681123 | A | G | 1 | a0001c0007t0012g0006 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-678-170T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681123 | |||||||
| chr17:15681137 | C | G | 26 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0084 others(23): Show |
28 | HG00544.hp2 HG00741.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-678-184G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681137 | |||||||
| chr17:15681257 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-678-304C>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681257 | |||||||
| chr17:15681339 | G | A | 3 | a0002c0002t0002g0271 a0002c0002t0002g0272 a0002c0002t0002g0273 |
3 | HG00673.hp2 HG02027.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-678-386C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681339 | |||||||
| chr17:15681348 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-678-395G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681348 | |||||||
| chr17:15681405 | C | T | 2 | a0001c0024t0007g0190 a0002c0002t0007g0191 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-678-452G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681405 | |||||||
| chr17:15681406 | C | T | 1 | a0001c0024t0007g0190 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-678-453G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681406 | |||||||
| chr17:15681488 | G | A | 1 | a0002c0002t0002g0274 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-678-535C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681488 | |||||||
| chr17:15681507 | T | C | 19 | a0001c0001t0002g0275 a0001c0001t0002g0281 a0002c0002t0002g0018 others(16): Show |
21 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.-678-554A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681507 | |||||||
| chr17:15681913 | C | T | 7 | a0001c0007t0007g0187 a0001c0024t0007g0190 a0002c0002t0007g0191 others(4): Show |
10 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-679+941G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15681913 | |||||||
| chr17:15682060 | G | T | 1 | a0001c0001t0001g0028 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-679+794C>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682060 | |||||||
| chr17:15682069 | T | C | 2 | a0002c0002t0002g0321 a0004c0003t0004g0322 |
2 | HG00609.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-679+785A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682069 | |||||||
| chr17:15682248 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-679+606C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682248 | |||||||
| chr17:15682480 | T | G | 2 | a0002c0005t0002g0292 a0002c0005t0002g0293 |
2 | NA18997.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-679+374A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682480 | |||||||
| chr17:15682501 | C | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(124): Show |
137 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(134): Show |
intron_variant | MODIFIER | c.-679+353G>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682501 | |||||||
| chr17:15682507 | G | A | 5 | a0002c0002t0009g0022 a0002c0002t0009g0026 a0003c0014t0015g0024 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-679+347C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682507 | |||||||
| chr17:15682621 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-679+233A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682621 | |||||||
| chr17:15682698 | T | G | 2 | a0003c0004t0003g0181 a0003c0004t0003g0182 |
2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-679+156A>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682698 | |||||||
| chr17:15682717 | C | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | NA18961.hp1 NA18999.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-679+137G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682717 | |||||||
| chr17:15682772 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-679+82C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682772 | |||||||
| chr17:15682836 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(114): Show |
126 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(123): Show |
intron_variant | MODIFIER | c.-679+18G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 3/11 | chr17 | 15682836 | |||||||
| chr17:15683251 | G | A | 1 | a0002c0002t0002g0294 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-898-94C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683251 | |||||||
| chr17:15683329 | G | A | 2 | a0001c0024t0007g0190 a0002c0002t0007g0191 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-898-172C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683329 | |||||||
| chr17:15683575 | A | G | 152 | a0001c0001t0002g0021 a0001c0001t0002g0198 a0001c0001t0002g0199 others(149): Show |
162 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-898-418T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683575 | |||||||
| chr17:15683611 | G | A | 1 | a0006c0009t0002g0295 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-898-454C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683611 | |||||||
| chr17:15683734 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-899+462A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683734 | |||||||
| chr17:15683762 | C | T | 3 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 |
3 | HG01891.hp1 HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-899+434G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683762 | |||||||
| chr17:15683775 | T | C | 31 | a0001c0001t0002g0021 a0001c0001t0002g0304 a0001c0001t0002g0305 others(28): Show |
33 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-899+421A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683775 | |||||||
| chr17:15683783 | C | T | 5 | a0002c0002t0009g0022 a0002c0002t0009g0026 a0003c0014t0015g0024 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-899+413G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683783 | |||||||
| chr17:15683867 | G | A | 9 | a0001c0001t0007g0192 a0001c0001t0007g0193 a0001c0001t0007g0194 others(6): Show |
10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-899+329C>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683867 | |||||||
| chr17:15683875 | T | C | 5 | a0002c0002t0009g0022 a0002c0002t0009g0026 a0003c0014t0015g0024 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-899+321A>G | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683875 | |||||||
| chr17:15683912 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
11 | HG01243.hp1 HG02647.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-899+284G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683912 | |||||||
| chr17:15683917 | C | T | 2 | a0003c0004t0003g0072 a0003c0004t0003g0073 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-899+279G>A | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683917 | |||||||
| chr17:15683986 | A | G | 286 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(283): Show |
309 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.-899+210T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15683986 | |||||||
| chr17:15684031 | A | G | 286 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(283): Show |
309 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.-899+165T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15684031 | |||||||
| chr17:15684055 | A | G | 1 | a0002c0002t0009g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-899+141T>C | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15684055 | |||||||
| chr17:15684089 | C | A | 286 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(283): Show |
309 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.-899+107G>T | TRIM16 | ENSG00000221926.13 | transcript | ENST00000649191.2 | protein_coding | 1/11 | chr17 | 15684089 |