Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6868 |
| ensemblid | ENSG00000151694.15 |
| hgncid | 195 |
| symbol | ADAM17 |
| name | ADAM metallopeptidase domain 17 |
| refseq_nuc | NM_003183.6 |
| refseq_prot | NP_003174.3 |
| ensembl_nuc | ENST00000310823.8 |
| ensembl_prot | ENSP00000309968.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 9488486 |
| end | 9555830 |
| strand | - |
| ver | v1.2 |
| region | chr2:9488486-9555830 |
| region5000 | chr2:9483486-9560830 |
| regionname0 | ADAM17_chr2_9488486_9555830 |
| regionname5000 | ADAM17_chr2_9483486_9560830 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 824 | 215 | 78 | 52 | 35 | 14 | 34 | 16 | ADAM17_chr2_9483486_9560830 | ADAM17 | MRQSL others(819): Show |
chr2 | 9483486 | 9560830 |
| a0002 | 0/0 | 824 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | MRQSL others(819): Show |
chr2 | 9483486 | 9560830 |
| a0003 | 0/0 | 824 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | MRQSL others(819): Show |
chr2 | 9483486 | 9560830 |
| a0004 | 0/0 | 824 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | MRQSL others(819): Show |
chr2 | 9483486 | 9560830 |
| a0005 | 0/0 | 824 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | MRQSL others(819): Show |
chr2 | 9483486 | 9560830 |
| a0006 | 0/0 | 824 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | MRQSL others(819): Show |
chr2 | 9483486 | 9560830 |
| a0007 | 0/0 | 824 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | MRQSL others(819): Show |
chr2 | 9483486 | 9560830 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2472 | 118 | 53 | 28 | 11 | 8 | 17 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0001c0002 | 1/0 | 2472 | 91 | 25 | 22 | 24 | 5 | 14 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0001c0005 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0001c0006 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0001c0008 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0001c0012 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0001c0013 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0001c0014 | 0/0 | 2472 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0002c0003 | 0/0 | 2472 | 13 | 10 | 3 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0003c0004 | 0/0 | 2472 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0004c0009 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0005c0007 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0006c0011 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 | ||
| a0007c0010 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | ATGAG others(2467): Show |
chr2 | 9483486 | 9560830 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4390 | 26 | 7 | 8 | 3 | 5 | 3 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0003 | 0/0 | 4391 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0004 | 0/0 | 4391 | 10 | 0 | 1 | 5 | 0 | 4 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0008 | 0/0 | 4392 | 8 | 0 | 5 | 0 | 1 | 2 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0009 | 0/0 | 4391 | 7 | 1 | 1 | 0 | 0 | 5 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0011 | 0/0 | 4390 | 5 | 4 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0012 | 0/0 | 4390 | 5 | 3 | 1 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0013 | 0/0 | 4390 | 5 | 1 | 4 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0017 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4402): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0018 | 0/0 | 4406 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4401): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0019 | 0/0 | 4393 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4388): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0020 | 0/0 | 4393 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4388): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0022 | 0/0 | 4391 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0023 | 0/0 | 4391 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0024 | 0/0 | 4391 | 2 | 1 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0026 | 0/0 | 4410 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4405): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0027 | 0/0 | 4405 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4400): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0028 | 0/0 | 4391 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0029 | 0/0 | 4392 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0030 | 0/0 | 4392 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0031 | 0/0 | 4390 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0032 | 0/0 | 4390 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0033 | 0/0 | 4389 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4384): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0034 | 0/1 | 4389 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4384): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0035 | 0/0 | 4390 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0036 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4402): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0048 | 0/0 | 4412 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4407): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0049 | 0/0 | 4408 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4403): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0050 | 0/0 | 4408 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4403): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0051 | 0/0 | 4404 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4399): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0052 | 0/0 | 4394 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4389): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0053 | 0/0 | 4393 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4388): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0054 | 0/0 | 4390 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0055 | 0/0 | 4408 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4403): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0056 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4384): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0057 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0058 | 0/0 | 4392 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0059 | 0/0 | 4413 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4408): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0060 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0062 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0065 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0066 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0001t0067 | 0/0 | 4393 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4388): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0002 | 1/0 | 4391 | 25 | 0 | 4 | 9 | 1 | 10 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0003 | 0/0 | 4391 | 10 | 4 | 3 | 1 | 1 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0005 | 0/0 | 4390 | 9 | 9 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0006 | 0/0 | 4391 | 8 | 1 | 7 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0007 | 0/0 | 4392 | 8 | 0 | 4 | 1 | 1 | 2 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0010 | 0/0 | 4393 | 6 | 0 | 1 | 4 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4388): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0014 | 0/0 | 4389 | 5 | 5 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4384): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0015 | 0/0 | 4390 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0016 | 0/0 | 4391 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0021 | 0/0 | 4392 | 3 | 1 | 0 | 2 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0032 | 0/0 | 4390 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0068 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0069 | 0/0 | 4389 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4384): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0070 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0071 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0072 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0074 | 0/0 | 4390 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0075 | 0/0 | 4392 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0076 | 0/0 | 4392 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0001c0002t0077 | 0/0 | 4393 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4388): Show |
chr2 | 9483486 | 9560830 |
| a0001c0005t0006 | 0/0 | 4391 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0006t0001 | 0/0 | 4390 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0008t0073 | 0/0 | 4391 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0001c0012t0001 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0013t0001 | 0/0 | 4390 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0001c0014t0007 | 0/0 | 4392 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0025 | 0/0 | 4405 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4400): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0038 | 0/0 | 4405 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4400): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0039 | 0/0 | 4426 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4421): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0040 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4417): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0041 | 0/0 | 4410 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4405): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0042 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4401): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0043 | 0/0 | 4396 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4391): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0044 | 0/0 | 4395 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4390): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0045 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4402): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0046 | 0/0 | 4406 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4401): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0047 | 0/0 | 4397 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4392): Show |
chr2 | 9483486 | 9560830 |
| a0002c0003t0063 | 0/0 | 4391 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0003c0004t0005 | 0/0 | 4390 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0003c0004t0016 | 0/0 | 4391 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0004c0009t0064 | 0/0 | 4390 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4385): Show |
chr2 | 9483486 | 9560830 |
| a0005c0007t0023 | 0/0 | 4391 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4386): Show |
chr2 | 9483486 | 9560830 |
| a0006c0011t0061 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4383): Show |
chr2 | 9483486 | 9560830 |
| a0007c0010t0037 | 0/0 | 4392 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | AGCGG others(4387): Show |
chr2 | 9483486 | 9560830 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0008g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0009g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0011g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0012g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0012g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0013g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0013g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0013g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0017g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0017g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0018g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0018g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0019g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0019g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0019g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0020g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0020g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0020g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0022g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0022g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0023g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0024g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0024g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0026g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0026g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0027g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0027g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0028g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0028g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0029g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0029g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0030g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0030g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0031g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0031g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0032g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0033g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0034g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0035g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0036g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0048g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0049g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0050g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0051g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0052g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0053g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0054g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0055g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0056g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0057g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0058g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0059g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0060g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0062g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0065g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0066g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0001t0067g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0007g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0007g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0007g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0007g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0010g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0010g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0010g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0010g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0014g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0014g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0014g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0015g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0015g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0015g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0015g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0016g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0021g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0021g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0021g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0032g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0068g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0069g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0070g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0071g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0072g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0074g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0075g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0076g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0002t0077g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0005t0006g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0006t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0008t0073g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0012t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0013t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0001c0014t0007g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0025g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0025g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0038g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0039g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0040g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0041g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0042g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0043g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0044g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0045g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0046g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0047g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0002c0003t0063g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0003c0004t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0003c0004t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0004c0009t0064g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0005c0007t0023g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0006c0011t0061g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| a0007c0010t0037g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0086 | EUR | GBR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00140 | hp1 | a0001 | c0002 | t0007 | g0195 | EUR | GBR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00140 | hp2 | a0001 | c0002 | t0068 | g0088 | EUR | GBR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00280 | hp1 | a0001 | c0001 | t0035 | g0039 | EUR | FIN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | CHS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00597 | hp2 | a0001 | c0002 | t0015 | g0174 | EAS | CHS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00621 | hp1 | a0001 | c0002 | t0010 | g0183 | EAS | CHS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00621 | hp2 | a0001 | c0002 | t0076 | g0201 | EAS | CHS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00639 | hp1 | a0001 | c0012 | t0001 | g0032 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00639 | hp2 | a0001 | c0001 | t0011 | g0113 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0139 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00642 | hp2 | a0001 | c0001 | t0028 | g0081 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG00738 | hp2 | a0002 | c0003 | t0025 | g0063 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01069 | hp2 | a0001 | c0002 | t0006 | g0221 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01070 | hp1 | a0001 | c0001 | t0013 | g0134 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01070 | hp2 | a0004 | c0009 | t0064 | g0143 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01071 | hp1 | a0001 | c0001 | t0013 | g0129 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01074 | hp1 | a0001 | c0001 | t0013 | g0125 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01099 | hp1 | a0001 | c0001 | t0023 | g0026 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0106 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01106 | hp1 | a0001 | c0001 | t0067 | g0132 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01106 | hp2 | a0001 | c0002 | t0006 | g0189 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01109 | hp1 | a0001 | c0001 | t0059 | g0099 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01109 | hp2 | a0002 | c0003 | t0043 | g0051 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01167 | hp1 | a0001 | c0002 | t0007 | g0209 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0090 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01175 | hp1 | a0001 | c0001 | t0033 | g0023 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01175 | hp2 | a0002 | c0003 | t0063 | g0142 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0133 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01243 | hp2 | a0001 | c0002 | t0006 | g0218 | AMR | PUR | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0122 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01256 | hp2 | a0001 | c0002 | t0006 | g0178 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0120 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01261 | hp2 | a0001 | c0001 | t0058 | g0080 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01346 | hp2 | a0001 | c0002 | t0075 | g0228 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0119 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01433 | hp1 | a0001 | c0002 | t0007 | g0184 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0121 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01496 | hp1 | a0001 | c0001 | t0048 | g0068 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01496 | hp2 | a0001 | c0002 | t0006 | g0217 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01515 | hp1 | a0001 | c0001 | t0028 | g0079 | EUR | IBS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0207 | EUR | IBS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01884 | hp1 | a0001 | c0001 | t0018 | g0096 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01884 | hp2 | a0001 | c0001 | t0019 | g0046 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01891 | hp1 | a0001 | c0001 | t0049 | g0097 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01928 | hp1 | a0001 | c0002 | t0007 | g0211 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01928 | hp2 | a0001 | c0002 | t0006 | g0220 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01934 | hp1 | a0001 | c0002 | t0006 | g0219 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01934 | hp2 | a0001 | c0001 | t0012 | g0116 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01952 | hp1 | a0001 | c0002 | t0071 | g0176 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01952 | hp2 | a0001 | c0002 | t0007 | g0223 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01978 | hp1 | a0001 | c0002 | t0072 | g0175 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01978 | hp2 | a0001 | c0002 | t0010 | g0222 | AMR | PEL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02027 | hp2 | a0001 | c0001 | t0057 | g0070 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02055 | hp1 | a0001 | c0001 | t0066 | g0041 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02055 | hp2 | a0002 | c0003 | t0038 | g0056 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02071 | hp1 | a0001 | c0002 | t0010 | g0227 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02071 | hp2 | a0001 | c0002 | t0010 | g0188 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02129 | hp2 | a0001 | c0002 | t0074 | g0212 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02135 | hp2 | a0001 | c0002 | t0007 | g0230 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02145 | hp1 | a0001 | c0002 | t0005 | g0157 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02145 | hp2 | a0001 | c0001 | t0036 | g0040 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | CDX | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | CDX | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | CDX | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02165 | hp2 | a0001 | c0001 | t0030 | g0082 | EAS | CDX | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02257 | hp1 | a0001 | c0001 | t0020 | g0100 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0155 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0127 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02258 | hp2 | a0001 | c0001 | t0017 | g0094 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02280 | hp1 | a0001 | c0002 | t0021 | g0206 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02280 | hp2 | a0001 | c0001 | t0056 | g0077 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02451 | hp1 | a0001 | c0001 | t0018 | g0050 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02451 | hp2 | a0002 | c0003 | t0044 | g0055 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02523 | hp2 | a0005 | c0007 | t0023 | g0008 | EAS | KHV | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02572 | hp1 | a0002 | c0003 | t0046 | g0062 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02572 | hp2 | a0002 | c0003 | t0040 | g0059 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0112 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02615 | hp2 | a0001 | c0002 | t0014 | g0163 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02622 | hp1 | a0001 | c0001 | t0024 | g0028 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0114 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02630 | hp1 | a0001 | c0001 | t0017 | g0048 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02630 | hp2 | a0001 | c0002 | t0014 | g0144 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0124 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02647 | hp2 | a0001 | c0001 | t0053 | g0047 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0210 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0145 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02717 | hp2 | a0001 | c0001 | t0050 | g0065 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0147 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0166 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0123 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0168 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02809 | hp2 | a0001 | c0001 | t0020 | g0085 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02886 | hp1 | a0001 | c0001 | t0029 | g0103 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02886 | hp2 | a0002 | c0003 | t0041 | g0057 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0151 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02895 | hp2 | a0001 | c0001 | t0029 | g0102 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02896 | hp1 | a0001 | c0002 | t0005 | g0154 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02896 | hp2 | a0001 | c0001 | t0051 | g0092 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02897 | hp1 | a0001 | c0001 | t0027 | g0093 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02897 | hp2 | a0001 | c0002 | t0069 | g0152 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02922 | hp2 | a0001 | c0001 | t0027 | g0098 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02965 | hp1 | a0003 | c0004 | t0005 | g0159 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02965 | hp2 | a0001 | c0001 | t0060 | g0087 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0111 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03017 | hp2 | a0001 | c0001 | t0012 | g0131 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03041 | hp2 | a0001 | c0001 | t0019 | g0043 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03098 | hp1 | a0001 | c0001 | t0026 | g0066 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03098 | hp2 | a0001 | c0001 | t0032 | g0064 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0044 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03130 | hp2 | a0001 | c0002 | t0014 | g0161 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03139 | hp1 | a0001 | c0001 | t0031 | g0108 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03139 | hp2 | a0001 | c0002 | t0016 | g0158 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03195 | hp1 | a0002 | c0003 | t0025 | g0061 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03195 | hp2 | a0001 | c0001 | t0062 | g0140 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0117 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03225 | hp2 | a0001 | c0001 | t0018 | g0095 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0126 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0181 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0076 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0167 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03486 | hp1 | a0002 | c0003 | t0042 | g0060 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0156 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03490 | hp1 | a0001 | c0008 | t0073 | g0180 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0170 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03516 | hp1 | a0001 | c0002 | t0016 | g0149 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03516 | hp2 | a0001 | c0001 | t0022 | g0036 | AFR | ESN | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03540 | hp1 | a0001 | c0002 | t0016 | g0150 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03540 | hp2 | a0001 | c0001 | t0065 | g0141 | AFR | GWD | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03579 | hp1 | a0001 | c0002 | t0070 | g0148 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03579 | hp2 | a0001 | c0001 | t0031 | g0109 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03654 | hp1 | a0001 | c0014 | t0007 | g0233 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03654 | hp2 | a0001 | c0001 | t0009 | g0136 | SAS | PJL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0101 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03834 | hp2 | a0001 | c0001 | t0009 | g0130 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03927 | hp1 | a0001 | c0002 | t0010 | g0203 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03927 | hp2 | a0001 | c0001 | t0009 | g0137 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03942 | hp1 | a0001 | c0002 | t0007 | g0215 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0138 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04184 | hp1 | a0001 | c0001 | t0030 | g0104 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04199 | hp1 | a0001 | c0013 | t0001 | g0010 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0072 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0208 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04204 | hp2 | a0001 | c0001 | t0009 | g0128 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0193 | SAS | STU | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA18522 | hp1 | a0001 | c0001 | t0026 | g0067 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA18522 | hp2 | a0001 | c0002 | t0014 | g0162 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA18906 | hp1 | a0001 | c0001 | t0055 | g0049 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA18906 | hp2 | a0001 | c0002 | t0014 | g0165 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA18950 | hp2 | a0001 | c0002 | t0010 | g0200 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA18979 | hp1 | a0001 | c0002 | t0021 | g0214 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA18979 | hp2 | a0001 | c0002 | t0021 | g0224 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19004 | hp1 | a0001 | c0002 | t0015 | g0172 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19007 | hp2 | a0001 | c0002 | t0015 | g0171 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19030 | hp2 | a0002 | c0003 | t0047 | g0052 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0118 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0115 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19068 | hp1 | a0001 | c0002 | t0015 | g0173 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19079 | hp2 | a0001 | c0002 | t0077 | g0182 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19091 | hp1 | a0001 | c0001 | t0024 | g0006 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19240 | hp1 | a0001 | c0001 | t0022 | g0037 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA19240 | hp2 | a0007 | c0010 | t0037 | g0053 | AFR | YRI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20129 | hp2 | a0001 | c0001 | t0054 | g0069 | AFR | ASW | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20752 | hp1 | a0001 | c0002 | t0032 | g0089 | EUR | TSI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20805 | hp1 | a0001 | c0006 | t0001 | g0004 | EUR | TSI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0135 | EUR | TSI | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20905 | hp1 | a0001 | c0002 | t0007 | g0232 | SAS | GIH | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG01123 | hp2 | a0001 | c0005 | t0006 | g0213 | AMR | CLM | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02109 | hp1 | a0001 | c0002 | t0005 | g0153 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02109 | hp2 | a0002 | c0003 | t0045 | g0058 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02486 | hp1 | a0001 | c0001 | t0017 | g0091 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG02486 | hp2 | a0001 | c0001 | t0052 | g0045 | AFR | ACB | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03471 | hp1 | a0001 | c0002 | t0005 | g0164 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0146 | AFR | MSL | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG06807 | hp1 | a0006 | c0011 | t0061 | g0107 | AFR | USA | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | USA | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20300 | hp1 | a0003 | c0004 | t0016 | g0160 | AFR | USA | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA20300 | hp2 | a0001 | c0002 | t0006 | g0216 | AFR | USA | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0110 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| NA21309 | hp2 | a0002 | c0003 | t0039 | g0054 | AFR | LWK | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0034 | g0019 | REF | REF | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0198 | REF | REF | ADAM17_chr2_9483486_9560830 | ADAM17 | chr2 | 9483486 | 9560830 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9490409 | G | A | 1 | a0007 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2243C>T | p.Ala748Val | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 2468/4391 | 2243/2475 | 748/824 | chr2 | 9490409 | |||
| chr2:9490412 | G | A | 1 | a0005 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.2240C>T | p.Ser747Leu | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 2465/4391 | 2240/2475 | 747/824 | chr2 | 9490412 | |||
| chr2:9505338 | T | C | 1 | a0004 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.1372A>G | p.Ile458Val | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/19 | 1597/4391 | 1372/2475 | 458/824 | chr2 | 9505338 | |||
| chr2:9527801 | T | C | 2 | a0002 a0007 |
14 | HG00738.hp2 HG01109.hp2 HG01175.hp2 others(11): Show |
missense_variant | MODERATE | c.604A>G | p.Arg202Gly | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/19 | 829/4391 | 604/2475 | 202/824 | chr2 | 9527801 | |||
| chr2:9527921 | T | C | 1 | a0006 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.484A>G | p.Lys162Glu | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/19 | 709/4391 | 484/2475 | 162/824 | chr2 | 9527921 | |||
| chr2:9536827 | G | C | 1 | a0003 | 2 | HG02965.hp1 NA20300.hp1 |
missense_variant&splice_region_variant | MODERATE | c.232C>G | p.His78Asp | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/19 | 457/4391 | 232/2475 | 78/824 | chr2 | 9536827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9490306 | G | A | 1 | a0001c0008 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.2346C>T | p.Phe782Phe | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 2571/4391 | 2346/2475 | 782/824 | chr2 | 9490306 | |||
| chr2:9494727 | A | G | 9 | a0001c0001 a0001c0006 a0001c0012 others(6): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
synonymous_variant | LOW | c.1824T>C | p.Ser608Ser | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/19 | 2049/4391 | 1824/2475 | 608/824 | chr2 | 9494727 | |||
| chr2:9497202 | A | G | 1 | a0001c0006 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1695T>C | p.Thr565Thr | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/19 | 1920/4391 | 1695/2475 | 565/824 | chr2 | 9497202 | |||
| chr2:9535849 | G | C | 1 | a0001c0012 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.435C>G | p.Ala145Ala | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/19 | 660/4391 | 435/2475 | 145/824 | chr2 | 9535849 | |||
| chr2:9535876 | A | G | 1 | a0001c0005 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.408T>C | p.Val136Val | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/19 | 633/4391 | 408/2475 | 136/824 | chr2 | 9535876 | |||
| chr2:9536738 | G | A | 1 | a0001c0013 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.321C>T | p.Tyr107Tyr | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/19 | 546/4391 | 321/2475 | 107/824 | chr2 | 9536738 | |||
| chr2:9555525 | G | A | 1 | a0001c0014 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.81C>T | p.Gly27Gly | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 306/4391 | 81/2475 | 27/824 | chr2 | 9555525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9488534 | A | G | 2 | a0001c0001t0028 a0001c0001t0058 |
3 | HG00642.hp2 HG01261.hp2 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1643T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1643 | chr2 | 9488534 | ||||||
| chr2:9488673 | A | G | 1 | a0002c0003t0046 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1504T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1504 | chr2 | 9488673 | ||||||
| chr2:9488692 | A | G | 3 | a0001c0002t0006 a0001c0002t0075 a0001c0005t0006 |
10 | HG01069.hp2 HG01106.hp2 HG01123.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1485T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1485 | chr2 | 9488692 | ||||||
| chr2:9488760 | C | G | 1 | a0001c0002t0070 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1417G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1417 | chr2 | 9488760 | ||||||
| chr2:9489151 | G | GT | 14 | a0001c0001t0004 a0001c0001t0017 a0001c0001t0018 others(11): Show |
31 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1025dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1025 | chr2 | 9489151 | ||||||
| chr2:9489151 | G | GTTT | 6 | a0001c0001t0012 a0001c0001t0019 a0001c0001t0052 others(3): Show |
12 | HG01884.hp2 HG01934.hp2 HG02486.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1025dupAAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1025 | chr2 | 9489151 | ||||||
| chr2:9489157 | T | TTTG | 11 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0011 others(8): Show |
34 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1017_*1019dupCAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1019 | chr2 | 9489157 | ||||||
| chr2:9489158 | TTG | T | 3 | a0001c0001t0020 a0001c0001t0056 a0001c0001t0060 |
5 | HG02257.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1017_*1018delCA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1017 | chr2 | 9489158 | ||||||
| chr2:9489160 | G | T | 2 | a0001c0002t0005 a0001c0002t0069 |
4 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1017C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1017 | chr2 | 9489160 | ||||||
| chr2:9489169 | G | A | 1 | a0001c0002t0070 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1008C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1008 | chr2 | 9489169 | ||||||
| chr2:9489169 | G | GTTC | 10 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0024 others(7): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1008insGAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 1007 | chr2 | 9489169 | ||||||
| chr2:9489198 | C | T | 1 | a0001c0001t0054 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 979 | chr2 | 9489198 | ||||||
| chr2:9489199 | A | G | 2 | a0001c0001t0019 a0001c0001t0052 |
4 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*978T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 978 | chr2 | 9489199 | ||||||
| chr2:9489238 | T | G | 27 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(24): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*939A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 939 | chr2 | 9489238 | ||||||
| chr2:9489259 | A | AT | 3 | a0001c0002t0010 a0001c0002t0021 a0001c0002t0068 |
10 | HG00140.hp2 HG00621.hp1 HG01978.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*917dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTT | 3 | a0001c0001t0019 a0001c0001t0053 a0002c0003t0044 |
5 | HG01884.hp2 HG02451.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*915_*917dupAAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTT | 5 | a0001c0001t0020 a0001c0001t0052 a0001c0001t0060 others(2): Show |
7 | HG01109.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*914_*917dupAAAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(6): Show |
3 | a0001c0001t0051 a0002c0003t0025 a0002c0003t0046 |
4 | HG00738.hp2 HG02572.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*905_*917dupAAAAAA others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(7): Show |
4 | a0001c0001t0027 a0002c0003t0038 a0002c0003t0042 others(1): Show |
5 | HG02055.hp2 HG02109.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*904_*917dupAAAAAA others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0018 | 3 | HG01884.hp1 HG02451.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*903_*917dupAAAAAA others(9): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0017 a0001c0001t0036 a0001c0001t0055 others(1): Show |
6 | HG01109.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*902_*917dupAAAAAA others(10): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0050 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901_*917dupAAAAAA others(11): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0049 a0002c0003t0041 |
2 | HG01891.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*900_*917dupAAAAAA others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0026 | 2 | HG03098.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*899_*917dupAAAAAA others(13): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0048 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896_*917dupAAAAAA others(16): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(23): Show |
1 | a0002c0003t0040 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*917_*918insAAAAAA others(24): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | A | ATTTTTTT others(27): Show |
1 | a0002c0003t0039 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*917_*918insAAAAAA others(28): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | AT | A | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(19): Show |
80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*917delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 917 | chr2 | 9489259 | ||||||
| chr2:9489259 | ATT | A | 8 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0012 others(5): Show |
29 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*916_*917delAA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 916 | chr2 | 9489259 | ||||||
| chr2:9489289 | A | G | 2 | a0001c0001t0019 a0001c0001t0052 |
4 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*888T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 888 | chr2 | 9489289 | ||||||
| chr2:9489416 | C | CAGTA | 20 | a0001c0001t0004 a0001c0001t0017 a0001c0001t0018 others(17): Show |
40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*757_*760dupTACT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 760 | chr2 | 9489416 | ||||||
| chr2:9489496 | T | A | 1 | a0001c0002t0076 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 681 | chr2 | 9489496 | ||||||
| chr2:9489602 | T | C | 18 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0022 others(15): Show |
50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*575A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 575 | chr2 | 9489602 | ||||||
| chr2:9489725 | C | CA | 15 | a0001c0002t0007 a0001c0002t0010 a0001c0002t0016 others(12): Show |
30 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*451dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 451 | chr2 | 9489725 | ||||||
| chr2:9489725 | C | CAA | 5 | a0001c0002t0077 a0002c0003t0045 a0002c0003t0046 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 NA19030.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451dupTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 451 | chr2 | 9489725 | ||||||
| chr2:9489725 | CA | C | 5 | a0001c0001t0008 a0001c0001t0032 a0001c0002t0014 others(2): Show |
16 | HG01099.hp2 HG01243.hp1 HG01255.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*451delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 451 | chr2 | 9489725 | ||||||
| chr2:9489725 | CAA | C | 1 | a0001c0001t0009 | 7 | HG00642.hp1 HG02647.hp1 HG03239.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451delTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 450 | chr2 | 9489725 | ||||||
| chr2:9489725 | CAAA | C | 5 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0024 others(2): Show |
14 | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*449_*451delTTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 449 | chr2 | 9489725 | ||||||
| chr2:9489725 | CAAAA | C | 16 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0022 others(13): Show |
48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*448_*451delTTTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 448 | chr2 | 9489725 | ||||||
| chr2:9489725 | CAAAAA | C | 13 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0020 others(10): Show |
28 | HG00597.hp1 HG00642.hp2 HG01346.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*447_*451delTTTTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 447 | chr2 | 9489725 | ||||||
| chr2:9489725 | CAAAAAA | C | 9 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0026 others(6): Show |
15 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*446_*451delTTTTTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 446 | chr2 | 9489725 | ||||||
| chr2:9489745 | A | C | 3 | a0001c0002t0015 a0001c0002t0071 a0001c0008t0073 |
6 | HG00597.hp2 HG01952.hp1 HG03490.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*432T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 432 | chr2 | 9489745 | ||||||
| chr2:9489797 | C | T | 1 | a0007c0010t0037 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 380 | chr2 | 9489797 | ||||||
| chr2:9489814 | T | TA | 46 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(43): Show |
121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*362dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 362 | chr2 | 9489814 | ||||||
| chr2:9489824 | C | A | 1 | a0001c0001t0060 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 353 | chr2 | 9489824 | ||||||
| chr2:9489887 | T | C | 23 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(20): Show |
76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*290A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 290 | chr2 | 9489887 | ||||||
| chr2:9490102 | C | T | 59 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(56): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*75G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 75 | chr2 | 9490102 | ||||||
| chr2:9490115 | AT | A | 47 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(44): Show |
121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*61delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 19/19 | 61 | chr2 | 9490115 | ||||||
| chr2:9555641 | C | A | 2 | a0001c0002t0071 a0001c0002t0072 |
2 | HG01952.hp1 HG01978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-36G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 36 | chr2 | 9555641 | ||||||
| chr2:9555643 | G | C | 1 | a0001c0001t0035 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 38 | chr2 | 9555643 | ||||||
| chr2:9555651 | C | T | 1 | a0001c0001t0036 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 46 | chr2 | 9555651 | ||||||
| chr2:9555759 | G | T | 10 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0023 others(7): Show |
37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-154C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 154 | chr2 | 9555759 | ||||||
| chr2:9555777 | A | G | 74 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(71): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
5_prime_UTR_variant | MODIFIER | c.-172T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/19 | 172 | chr2 | 9555777 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9490529 | A | G | 2 | a0001c0002t0015g0172 a0001c0002t0015g0173 |
2 | NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2134-11T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 18/18 | chr2 | 9490529 | |||||||
| chr2:9490879 | T | C | 1 | a0007c0010t0037g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2133+222A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 18/18 | chr2 | 9490879 | |||||||
| chr2:9491211 | T | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.2083-60A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491211 | |||||||
| chr2:9491507 | C | T | 2 | a0001c0001t0008g0119 a0001c0002t0016g0150 |
2 | HG01358.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2083-356G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491507 | |||||||
| chr2:9491593 | T | TCTC | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2083-445_2083-443d others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491593 | |||||||
| chr2:9491658 | A | G | 1 | a0001c0001t0050g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2083-507T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491658 | |||||||
| chr2:9491705 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2083-554T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9491705 | |||||||
| chr2:9492130 | T | C | 1 | a0001c0002t0007g0195 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2082+768A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492130 | |||||||
| chr2:9492202 | G | A | 2 | a0001c0001t0028g0079 a0001c0001t0058g0080 |
2 | HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2082+696C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492202 | |||||||
| chr2:9492269 | G | T | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+629C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492269 | |||||||
| chr2:9492443 | G | A | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+455C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492443 | |||||||
| chr2:9492542 | G | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2082+356C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492542 | |||||||
| chr2:9492589 | C | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(116): Show |
119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2082+309G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492589 | |||||||
| chr2:9492673 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2082+225A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492673 | |||||||
| chr2:9492768 | CAA | C | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2082+128_2082+129d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492768 | |||||||
| chr2:9492808 | G | A | 2 | a0001c0001t0026g0066 a0001c0001t0026g0067 |
2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2082+90C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492808 | |||||||
| chr2:9492846 | G | A | 11 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0039g0054 others(8): Show |
11 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2082+52C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 17/18 | chr2 | 9492846 | |||||||
| chr2:9493008 | T | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(133): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1994-22A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 16/18 | chr2 | 9493008 | |||||||
| chr2:9493287 | G | T | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1994-301C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 16/18 | chr2 | 9493287 | |||||||
| chr2:9493402 | A | G | 2 | a0002c0003t0043g0051 a0002c0003t0047g0052 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1993+345T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 16/18 | chr2 | 9493402 | |||||||
| chr2:9493922 | A | G | 2 | a0001c0001t0001g0007 a0004c0009t0064g0143 |
2 | HG01070.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1915-97T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9493922 | |||||||
| chr2:9493928 | A | T | 1 | a0001c0002t0006g0189 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1915-103T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9493928 | |||||||
| chr2:9493971 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1915-146C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9493971 | |||||||
| chr2:9494112 | A | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1915-287T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494112 | |||||||
| chr2:9494252 | C | T | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1914+385G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494252 | |||||||
| chr2:9494483 | C | T | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1914+154G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494483 | |||||||
| chr2:9494573 | A | T | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1914+64T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494573 | |||||||
| chr2:9494578 | T | C | 1 | a0001c0001t0008g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1914+59A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 15/18 | chr2 | 9494578 | |||||||
| chr2:9494813 | G | A | 12 | a0002c0003t0025g0063 a0002c0003t0038g0056 a0002c0003t0039g0054 others(9): Show |
12 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1784-46C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9494813 | |||||||
| chr2:9494925 | A | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-158T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9494925 | |||||||
| chr2:9495008 | T | C | 2 | a0001c0001t0029g0102 a0001c0001t0029g0103 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1784-241A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495008 | |||||||
| chr2:9495451 | G | A | 4 | a0001c0002t0005g0151 a0001c0002t0005g0153 a0001c0002t0005g0154 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1784-684C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495451 | |||||||
| chr2:9495669 | G | A | 10 | a0001c0002t0003g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1784-902C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495669 | |||||||
| chr2:9495711 | C | CA | 48 | a0001c0001t0032g0064 a0001c0002t0002g0187 a0001c0002t0003g0147 others(45): Show |
48 | HG00597.hp2 HG00738.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.1784-945dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495711 | |||||||
| chr2:9495711 | C | CAA | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(118): Show |
121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1784-946_1784-945d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495711 | |||||||
| chr2:9495730 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1784-963G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495730 | |||||||
| chr2:9495748 | A | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1784-981T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495748 | |||||||
| chr2:9495784 | G | A | 3 | a0001c0001t0028g0079 a0001c0001t0028g0081 a0001c0001t0058g0080 |
3 | HG00642.hp2 HG01261.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1784-1017C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495784 | |||||||
| chr2:9495860 | C | CT | 5 | a0001c0001t0001g0027 a0001c0001t0050g0065 a0001c0002t0002g0225 others(2): Show |
5 | HG01891.hp2 HG02717.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784-1094dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495860 | |||||||
| chr2:9495860 | CT | C | 38 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(35): Show |
38 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1784-1094delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9495860 | |||||||
| chr2:9496188 | G | A | 1 | a0001c0001t0012g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1783+926C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496188 | |||||||
| chr2:9496219 | C | T | 1 | a0002c0003t0047g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1783+895G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496219 | |||||||
| chr2:9496305 | T | C | 41 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(38): Show |
41 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1783+809A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496305 | |||||||
| chr2:9496321 | C | T | 4 | a0001c0001t0031g0108 a0001c0001t0031g0109 a0001c0001t0066g0041 others(1): Show |
4 | HG01175.hp2 HG02055.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783+793G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496321 | |||||||
| chr2:9496430 | CTCTG | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1783+680_1783+683d others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496430 | |||||||
| chr2:9496444 | A | AAAGCAAG others(14): Show |
1 | a0001c0001t0066g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1783+649_1783+669d others(23): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496444 | |||||||
| chr2:9496466 | G | A | 1 | a0001c0002t0002g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1783+648C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496466 | |||||||
| chr2:9496679 | TGG | T | 7 | a0001c0001t0022g0036 a0001c0001t0022g0037 a0001c0001t0031g0108 others(4): Show |
7 | HG01175.hp2 HG02055.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1783+433_1783+434d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496679 | |||||||
| chr2:9496882 | G | A | 3 | a0001c0001t0022g0036 a0001c0001t0022g0037 a0001c0001t0066g0041 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1783+232C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496882 | |||||||
| chr2:9496889 | A | G | 1 | a0001c0002t0021g0224 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1783+225T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496889 | |||||||
| chr2:9496939 | A | G | 1 | a0002c0003t0047g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1783+175T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496939 | |||||||
| chr2:9496956 | C | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1783+158G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9496956 | |||||||
| chr2:9497003 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1783+111G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 14/18 | chr2 | 9497003 | |||||||
| chr2:9497274 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1649-26T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9497274 | |||||||
| chr2:9497593 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1649-345G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9497593 | |||||||
| chr2:9498185 | A | G | 1 | a0001c0001t0050g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1649-937T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498185 | |||||||
| chr2:9498197 | TTTTC | T | 40 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(37): Show |
40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1649-953_1649-950d others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498197 | |||||||
| chr2:9498252 | A | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1649-1004T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498252 | |||||||
| chr2:9498295 | G | C | 1 | a0002c0003t0063g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1649-1047C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498295 | |||||||
| chr2:9498300 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1649-1052C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498300 | |||||||
| chr2:9498487 | T | C | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-1239A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9498487 | |||||||
| chr2:9499065 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1649-1817G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499065 | |||||||
| chr2:9499102 | T | C | 1 | a0002c0003t0038g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1649-1854A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499102 | |||||||
| chr2:9499110 | CTTCTTTT | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1649-1869_1649-186 others(11): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499110 | |||||||
| chr2:9499113 | C | CT | 32 | a0001c0001t0032g0064 a0001c0002t0002g0187 a0001c0002t0002g0231 others(29): Show |
32 | HG00597.hp2 HG01978.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1649-1866dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499113 | |||||||
| chr2:9499113 | C | CTTT | 11 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0039g0054 others(8): Show |
11 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1649-1868_1649-186 others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499113 | |||||||
| chr2:9499192 | C | A | 40 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(37): Show |
40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1649-1944G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499192 | |||||||
| chr2:9499241 | T | C | 1 | a0001c0001t0004g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1649-1993A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499241 | |||||||
| chr2:9499470 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1649-2222G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499470 | |||||||
| chr2:9499488 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1649-2240C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499488 | |||||||
| chr2:9499546 | C | T | 1 | a0001c0002t0007g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1649-2298G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499546 | |||||||
| chr2:9499590 | C | G | 10 | a0001c0002t0006g0178 a0001c0002t0006g0189 a0001c0002t0006g0216 others(7): Show |
10 | HG01069.hp2 HG01106.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649-2342G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499590 | |||||||
| chr2:9499593 | A | G | 10 | a0001c0002t0006g0178 a0001c0002t0006g0189 a0001c0002t0006g0216 others(7): Show |
10 | HG01069.hp2 HG01106.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649-2345T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499593 | |||||||
| chr2:9499615 | G | A | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-2367C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499615 | |||||||
| chr2:9499697 | G | A | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1649-2449C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499697 | |||||||
| chr2:9499786 | C | T | 1 | a0001c0001t0057g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1648+2387G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9499786 | |||||||
| chr2:9500021 | T | C | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1648+2152A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500021 | |||||||
| chr2:9500088 | CATAG | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1648+2081_1648+208 others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500088 | |||||||
| chr2:9500116 | T | C | 2 | a0001c0001t0029g0102 a0001c0001t0029g0103 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1648+2057A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500116 | |||||||
| chr2:9500397 | T | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1648+1776A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500397 | |||||||
| chr2:9500775 | A | G | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1648+1398T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9500775 | |||||||
| chr2:9501029 | G | A | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648+1144C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501029 | |||||||
| chr2:9501068 | G | GTAA | 4 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0042g0060 others(1): Show |
4 | HG00738.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648+1104_1648+110 others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501068 | |||||||
| chr2:9501069 | C | A | 4 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0042g0060 others(1): Show |
4 | HG00738.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648+1104G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501069 | |||||||
| chr2:9501069 | C | CAAA | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1648+1103_1648+110 others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501069 | |||||||
| chr2:9501302 | G | C | 2 | a0001c0001t0029g0102 a0001c0001t0029g0103 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1648+871C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501302 | |||||||
| chr2:9501335 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(17): Show |
20 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1648+838C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501335 | |||||||
| chr2:9501623 | A | G | 38 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(35): Show |
38 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1648+550T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9501623 | |||||||
| chr2:9502023 | G | T | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1648+150C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 13/18 | chr2 | 9502023 | |||||||
| chr2:9502349 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1545-73G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502349 | |||||||
| chr2:9502392 | C | T | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1545-116G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502392 | |||||||
| chr2:9502408 | A | T | 1 | a0001c0001t0011g0113 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1545-132T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502408 | |||||||
| chr2:9502423 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1545-147G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502423 | |||||||
| chr2:9502601 | G | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1545-325C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502601 | |||||||
| chr2:9502740 | G | A | 1 | a0001c0001t0011g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1545-464C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502740 | |||||||
| chr2:9502749 | C | T | 1 | a0001c0002t0005g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1545-473G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502749 | |||||||
| chr2:9502827 | C | T | 22 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(19): Show |
22 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1545-551G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502827 | |||||||
| chr2:9502879 | C | CA | 35 | a0001c0001t0009g0126 a0001c0001t0011g0110 a0001c0001t0011g0111 others(32): Show |
35 | HG00639.hp2 HG00738.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1545-604dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502879 | |||||||
| chr2:9502879 | C | CAA | 23 | a0001c0001t0008g0106 a0001c0001t0008g0121 a0001c0001t0008g0122 others(20): Show |
23 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1545-605_1545-604d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502879 | |||||||
| chr2:9502879 | CA | C | 40 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(37): Show |
40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1545-604delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502879 | |||||||
| chr2:9502879 | CAA | C | 7 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(4): Show |
7 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1545-605_1545-604d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502879 | |||||||
| chr2:9502933 | G | A | 1 | a0001c0001t0031g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1545-657C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9502933 | |||||||
| chr2:9503128 | A | C | 40 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(37): Show |
40 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1545-852T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503128 | |||||||
| chr2:9503137 | C | CA | 42 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(39): Show |
42 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1545-862dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503137 | |||||||
| chr2:9503140 | AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0002g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1545-883_1545-865d others(21): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503140 | |||||||
| chr2:9503142 | A | G | 1 | a0001c0002t0014g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1545-866T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503142 | |||||||
| chr2:9503153 | G | C | 1 | a0001c0001t0009g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1545-877C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503153 | |||||||
| chr2:9503189 | A | C | 38 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(35): Show |
38 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1545-913T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503189 | |||||||
| chr2:9503212 | C | T | 1 | a0001c0002t0002g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1545-936G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503212 | |||||||
| chr2:9503249 | C | T | 1 | a0001c0001t0004g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1545-973G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503249 | |||||||
| chr2:9503317 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1545-1041A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503317 | |||||||
| chr2:9503400 | A | G | 4 | a0001c0001t0026g0066 a0001c0001t0026g0067 a0001c0001t0048g0068 others(1): Show |
4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545-1124T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503400 | |||||||
| chr2:9503559 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1545-1283T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503559 | |||||||
| chr2:9503781 | T | A | 4 | a0001c0002t0002g0187 a0001c0002t0002g0202 a0001c0002t0010g0183 others(1): Show |
4 | HG00621.hp1 HG00621.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1544+1385A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503781 | |||||||
| chr2:9503837 | C | CA | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1544+1328dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503837 | |||||||
| chr2:9503853 | G | A | 1 | a0007c0010t0037g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1544+1313C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503853 | |||||||
| chr2:9503854 | A | G | 1 | a0007c0010t0037g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1544+1312T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503854 | |||||||
| chr2:9503857 | T | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1544+1309A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503857 | |||||||
| chr2:9503857 | T | G | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1544+1309A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9503857 | |||||||
| chr2:9504007 | T | C | 1 | a0001c0001t0055g0049 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1544+1159A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504007 | |||||||
| chr2:9504029 | TA | T | 2 | a0001c0001t0004g0072 a0001c0001t0004g0101 |
2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1544+1136delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504029 | |||||||
| chr2:9504115 | C | T | 1 | a0001c0002t0007g0184 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1544+1051G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504115 | |||||||
| chr2:9504175 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
108 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1544+991C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504175 | |||||||
| chr2:9504252 | C | G | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1544+914G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504252 | |||||||
| chr2:9504253 | T | C | 8 | a0001c0001t0026g0066 a0001c0001t0026g0067 a0001c0001t0048g0068 others(5): Show |
8 | HG01496.hp1 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544+913A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504253 | |||||||
| chr2:9504464 | A | G | 1 | a0001c0002t0002g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1544+702T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504464 | |||||||
| chr2:9504471 | A | T | 1 | a0002c0003t0044g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1544+695T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504471 | |||||||
| chr2:9504523 | T | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(34): Show |
37 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1544+643A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504523 | |||||||
| chr2:9504533 | A | C | 7 | a0001c0002t0003g0166 a0001c0002t0005g0164 a0001c0002t0014g0161 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1544+633T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504533 | |||||||
| chr2:9504593 | C | T | 8 | a0001c0002t0003g0169 a0001c0002t0015g0171 a0001c0002t0015g0172 others(5): Show |
8 | HG00597.hp2 HG01952.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1544+573G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504593 | |||||||
| chr2:9504619 | C | G | 38 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(35): Show |
38 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1544+547G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504619 | |||||||
| chr2:9504633 | C | G | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1544+533G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504633 | |||||||
| chr2:9504717 | G | A | 12 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(9): Show |
12 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1544+449C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504717 | |||||||
| chr2:9504719 | G | A | 38 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(35): Show |
38 | HG00597.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1544+447C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504719 | |||||||
| chr2:9504751 | A | G | 1 | a0001c0001t0020g0100 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1544+415T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504751 | |||||||
| chr2:9504763 | GA | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
70 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1544+402delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504763 | |||||||
| chr2:9504870 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1544+296A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9504870 | |||||||
| chr2:9505030 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02135.hp1 NA19070.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1544+136C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9505030 | |||||||
| chr2:9505128 | T | C | 5 | a0001c0001t0011g0110 a0001c0001t0011g0111 a0001c0001t0011g0112 others(2): Show |
5 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1544+38A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 12/18 | chr2 | 9505128 | |||||||
| chr2:9505400 | A | C | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1345-35T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505400 | |||||||
| chr2:9505503 | C | A | 1 | a0001c0001t0013g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1345-138G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505503 | |||||||
| chr2:9505554 | A | G | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1345-189T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505554 | |||||||
| chr2:9505660 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1345-295G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505660 | |||||||
| chr2:9505824 | TCTC | T | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1345-462_1345-460d others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505824 | |||||||
| chr2:9505929 | A | G | 2 | a0001c0001t0029g0102 a0001c0001t0029g0103 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1345-564T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505929 | |||||||
| chr2:9505951 | C | T | 3 | a0001c0001t0013g0120 a0001c0001t0013g0129 a0001c0001t0013g0134 |
3 | HG01070.hp1 HG01071.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1345-586G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9505951 | |||||||
| chr2:9506259 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1345-894G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506259 | |||||||
| chr2:9506359 | G | GT | 43 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0021 others(40): Show |
43 | HG00140.hp2 HG01109.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1345-995dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506359 | |||||||
| chr2:9506359 | G | GTT | 6 | a0001c0001t0011g0112 a0001c0001t0030g0104 a0001c0001t0057g0070 others(3): Show |
6 | HG00140.hp1 HG02027.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-996_1345-995d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506359 | |||||||
| chr2:9506359 | GT | G | 5 | a0001c0001t0013g0134 a0001c0002t0002g0181 a0001c0002t0002g0191 others(2): Show |
5 | HG00738.hp1 HG01070.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-995delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506359 | |||||||
| chr2:9506359 | GTT | G | 5 | a0001c0001t0020g0076 a0001c0001t0020g0085 a0001c0001t0020g0100 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-996_1345-995d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506359 | |||||||
| chr2:9506366 | T | G | 1 | a0001c0002t0002g0185 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1345-1001A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506366 | |||||||
| chr2:9506394 | G | A | 1 | a0001c0002t0002g0186 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1345-1029C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506394 | |||||||
| chr2:9506440 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1345-1075A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506440 | |||||||
| chr2:9506656 | G | A | 1 | a0001c0002t0007g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1345-1291C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506656 | |||||||
| chr2:9506762 | G | A | 3 | a0001c0001t0031g0108 a0001c0001t0031g0109 a0002c0003t0063g0142 |
3 | HG01175.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1345-1397C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506762 | |||||||
| chr2:9506881 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-1516G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506881 | |||||||
| chr2:9506882 | G | T | 2 | a0002c0003t0038g0056 a0007c0010t0037g0053 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1345-1517C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506882 | |||||||
| chr2:9506892 | C | G | 2 | a0001c0001t0023g0026 a0005c0007t0023g0008 |
2 | HG01099.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1345-1527G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506892 | |||||||
| chr2:9506962 | A | C | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1345-1597T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9506962 | |||||||
| chr2:9507234 | A | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1345-1869T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507234 | |||||||
| chr2:9507416 | C | T | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1345-2051G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507416 | |||||||
| chr2:9507480 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1345-2115G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507480 | |||||||
| chr2:9507498 | C | A | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1345-2133G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507498 | |||||||
| chr2:9507508 | C | A | 1 | a0002c0003t0041g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1345-2143G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507508 | |||||||
| chr2:9507730 | CT | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(32): Show |
35 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1344+2248delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507730 | |||||||
| chr2:9507786 | C | T | 1 | a0001c0001t0004g0101 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1344+2193G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9507786 | |||||||
| chr2:9508086 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1344+1893G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508086 | |||||||
| chr2:9508245 | G | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
133 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1344+1734C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508245 | |||||||
| chr2:9508558 | C | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1344+1421G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508558 | |||||||
| chr2:9508614 | A | G | 6 | a0001c0001t0022g0036 a0001c0001t0022g0037 a0001c0001t0031g0108 others(3): Show |
6 | HG01175.hp2 HG02055.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+1365T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508614 | |||||||
| chr2:9508699 | C | A | 2 | a0001c0001t0022g0036 a0001c0001t0022g0037 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1344+1280G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508699 | |||||||
| chr2:9508757 | T | C | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1344+1222A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508757 | |||||||
| chr2:9508859 | G | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1344+1120C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508859 | |||||||
| chr2:9508991 | C | CA | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1344+987dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9508991 | |||||||
| chr2:9509837 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1344+142T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 11/18 | chr2 | 9509837 | |||||||
| chr2:9510221 | C | CATAA | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1192-91_1192-90ins others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510221 | |||||||
| chr2:9510581 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-450A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510581 | |||||||
| chr2:9510650 | C | T | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1192-519G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510650 | |||||||
| chr2:9510658 | C | T | 1 | a0001c0001t0012g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1192-527G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510658 | |||||||
| chr2:9510663 | C | CA | 6 | a0001c0001t0008g0123 a0001c0001t0011g0114 a0001c0001t0030g0082 others(3): Show |
6 | HG02165.hp2 HG02622.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-533dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510663 | |||||||
| chr2:9510663 | CA | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-533delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510663 | |||||||
| chr2:9510669 | A | G | 1 | a0001c0002t0072g0175 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1192-538T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510669 | |||||||
| chr2:9510932 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1192-801C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9510932 | |||||||
| chr2:9511319 | G | A | 1 | a0001c0002t0021g0214 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1192-1188C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511319 | |||||||
| chr2:9511335 | G | A | 1 | a0001c0001t0022g0037 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1192-1204C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511335 | |||||||
| chr2:9511343 | G | A | 1 | a0001c0002t0007g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1192-1212C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511343 | |||||||
| chr2:9511596 | G | C | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1192-1465C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511596 | |||||||
| chr2:9511615 | T | C | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1192-1484A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511615 | |||||||
| chr2:9511647 | A | T | 1 | a0001c0001t0001g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1192-1516T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511647 | |||||||
| chr2:9511764 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1192-1633T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511764 | |||||||
| chr2:9511855 | C | G | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-1724G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9511855 | |||||||
| chr2:9512017 | ACTTAAAA others(3): Show |
A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1192-1896_1192-188 others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512017 | |||||||
| chr2:9512092 | A | G | 1 | a0001c0002t0074g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1192-1961T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512092 | |||||||
| chr2:9512140 | G | A | 1 | a0002c0003t0063g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1192-2009C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512140 | |||||||
| chr2:9512258 | TA | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1192-2128delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512258 | |||||||
| chr2:9512446 | A | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-2315T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512446 | |||||||
| chr2:9512496 | T | C | 4 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0042g0060 others(1): Show |
4 | HG00738.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-2365A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512496 | |||||||
| chr2:9512616 | A | T | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-2485T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512616 | |||||||
| chr2:9512694 | A | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-2563T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9512694 | |||||||
| chr2:9513038 | G | A | 11 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0039g0054 others(8): Show |
11 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1192-2907C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513038 | |||||||
| chr2:9513288 | C | G | 1 | a0001c0001t0050g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1192-3157G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513288 | |||||||
| chr2:9513558 | G | A | 1 | a0001c0001t0030g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1192-3427C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513558 | |||||||
| chr2:9513598 | G | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192-3467C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513598 | |||||||
| chr2:9513601 | A | C | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1192-3470T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513601 | |||||||
| chr2:9513784 | G | T | 1 | a0001c0001t0009g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1192-3653C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513784 | |||||||
| chr2:9513908 | GA | G | 13 | a0001c0001t0017g0048 a0001c0001t0017g0091 a0001c0001t0017g0094 others(10): Show |
13 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1192-3778delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513908 | |||||||
| chr2:9513935 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1192-3804G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9513935 | |||||||
| chr2:9514010 | C | CA | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(43): Show |
46 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.1192-3880dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514010 | |||||||
| chr2:9514154 | T | C | 1 | a0001c0002t0076g0201 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1191+3747A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514154 | |||||||
| chr2:9514206 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+3695A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514206 | |||||||
| chr2:9514299 | T | C | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191+3602A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514299 | |||||||
| chr2:9514472 | C | A | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1191+3429G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514472 | |||||||
| chr2:9514493 | T | C | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1191+3408A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514493 | |||||||
| chr2:9514516 | T | A | 1 | a0001c0002t0002g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1191+3385A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514516 | |||||||
| chr2:9514517 | A | T | 1 | a0001c0002t0002g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1191+3384T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514517 | |||||||
| chr2:9514518 | A | AAT | 11 | a0001c0001t0001g0020 a0001c0001t0018g0095 a0001c0001t0065g0141 others(8): Show |
11 | HG01123.hp1 HG01167.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1191+3381_1191+338 others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATAT | 16 | a0001c0001t0017g0048 a0001c0001t0018g0050 a0001c0001t0048g0068 others(13): Show |
16 | HG00140.hp1 HG00597.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1191+3379_1191+338 others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATATAT | 9 | a0001c0001t0017g0094 a0001c0002t0002g0177 a0001c0002t0002g0192 others(6): Show |
9 | HG01358.hp1 HG01928.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+3377_1191+338 others(10): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATATATA others(1): Show |
13 | a0001c0001t0026g0066 a0001c0001t0026g0067 a0001c0001t0036g0040 others(10): Show |
13 | HG01106.hp2 HG01256.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.1191+3375_1191+338 others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATATATA others(3): Show |
7 | a0001c0001t0018g0096 a0001c0001t0027g0093 a0001c0001t0051g0092 others(4): Show |
7 | HG01884.hp1 HG01978.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1191+3373_1191+338 others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATATATA others(5): Show |
6 | a0001c0001t0017g0091 a0001c0001t0020g0076 a0001c0001t0027g0098 others(3): Show |
6 | HG02135.hp2 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1191+3371_1191+338 others(16): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATATATA others(7): Show |
3 | a0001c0002t0006g0218 a0001c0002t0006g0221 a0001c0002t0069g0152 |
3 | HG01069.hp2 HG01243.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1191+3369_1191+338 others(18): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATATATA others(9): Show |
5 | a0001c0001t0059g0099 a0001c0002t0002g0231 a0001c0002t0003g0167 others(2): Show |
5 | HG01109.hp1 HG02523.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3367_1191+338 others(20): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATATATA others(13): Show |
1 | a0001c0002t0010g0203 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1191+3363_1191+338 others(24): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | A | AATATATA others(15): Show |
1 | a0001c0002t0002g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1191+3361_1191+338 others(26): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AAT | A | 4 | a0001c0001t0001g0014 a0001c0001t0032g0064 a0001c0002t0006g0217 others(1): Show |
4 | HG01496.hp2 HG03098.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+3381_1191+338 others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATAT | A | 6 | a0001c0001t0001g0003 a0001c0002t0002g0179 a0001c0002t0002g0185 others(3): Show |
6 | HG01074.hp2 HG01433.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1191+3377_1191+338 others(10): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(1): Show |
A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0018 others(2): Show |
5 | HG00099.hp2 HG01257.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3375_1191+338 others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(3): Show |
A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0023g0026 others(4): Show |
7 | HG00639.hp1 HG01099.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1191+3373_1191+338 others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(5): Show |
A | 4 | a0001c0001t0001g0027 a0001c0001t0024g0028 a0001c0002t0005g0145 others(1): Show |
4 | HG01070.hp2 HG01891.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+3371_1191+338 others(16): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(7): Show |
A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(23): Show |
26 | HG00280.hp1 HG00280.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1191+3369_1191+338 others(18): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(9): Show |
A | 6 | a0001c0001t0001g0013 a0001c0001t0054g0069 a0001c0001t0056g0077 others(3): Show |
6 | HG02280.hp2 HG03490.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1191+3367_1191+338 others(20): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(11): Show |
A | 7 | a0001c0001t0008g0123 a0001c0001t0019g0043 a0001c0001t0019g0044 others(4): Show |
7 | HG01175.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1191+3365_1191+338 others(22): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(13): Show |
A | 15 | a0001c0001t0008g0106 a0001c0001t0009g0136 a0001c0001t0022g0036 others(12): Show |
15 | HG00621.hp1 HG00621.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1191+3363_1191+338 others(24): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(15): Show |
A | 9 | a0001c0001t0008g0135 a0001c0001t0011g0110 a0001c0001t0011g0111 others(6): Show |
9 | HG00639.hp2 HG01109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+3361_1191+338 others(26): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(17): Show |
A | 36 | a0001c0001t0008g0119 a0001c0001t0008g0121 a0001c0001t0008g0122 others(33): Show |
36 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1191+3359_1191+338 others(28): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(25): Show |
A | 22 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(19): Show |
23 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1191+3351_1191+338 others(36): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(27): Show |
A | 1 | a0001c0002t0014g0161 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1191+3349_1191+338 others(38): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514518 | AATATATA others(31): Show |
A | 1 | a0001c0001t0020g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1191+3345_1191+338 others(42): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514518 | |||||||
| chr2:9514568 | T | TATATATA others(3): Show |
1 | a0001c0002t0014g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1191+3332_1191+333 others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514568 | |||||||
| chr2:9514570 | A | T | 2 | a0001c0001t0020g0076 a0001c0002t0003g0167 |
2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1191+3331T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514570 | |||||||
| chr2:9514574 | A | T | 2 | a0001c0002t0010g0188 a0001c0002t0010g0227 |
2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1191+3327T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514574 | |||||||
| chr2:9514576 | A | T | 2 | a0001c0002t0010g0188 a0001c0002t0010g0227 |
2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1191+3325T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514576 | |||||||
| chr2:9514602 | G | A | 3 | a0001c0001t0022g0036 a0001c0001t0022g0037 a0001c0001t0066g0041 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1191+3299C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514602 | |||||||
| chr2:9514604 | T | C | 1 | a0001c0002t0003g0167 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1191+3297A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514604 | |||||||
| chr2:9514621 | T | C | 5 | a0001c0001t0054g0069 a0001c0002t0002g0192 a0001c0002t0002g0193 others(2): Show |
5 | HG03492.hp1 HG03834.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3280A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514621 | |||||||
| chr2:9514625 | A | G | 5 | a0001c0001t0054g0069 a0001c0002t0002g0192 a0001c0002t0002g0193 others(2): Show |
5 | HG03492.hp1 HG03834.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1191+3276T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514625 | |||||||
| chr2:9514674 | C | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1191+3227G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514674 | |||||||
| chr2:9514837 | T | C | 1 | a0001c0002t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1191+3064A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514837 | |||||||
| chr2:9514985 | C | T | 26 | a0001c0001t0017g0048 a0001c0001t0017g0091 a0001c0001t0017g0094 others(23): Show |
26 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1191+2916G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9514985 | |||||||
| chr2:9515002 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1191+2899T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515002 | |||||||
| chr2:9515018 | C | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191+2883G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515018 | |||||||
| chr2:9515097 | T | C | 3 | a0001c0001t0011g0110 a0001c0001t0011g0113 a0001c0001t0011g0114 |
3 | HG00639.hp2 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1191+2804A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515097 | |||||||
| chr2:9515111 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+2790A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515111 | |||||||
| chr2:9515131 | T | C | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1191+2770A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515131 | |||||||
| chr2:9515155 | A | C | 1 | a0001c0001t0066g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1191+2746T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515155 | |||||||
| chr2:9515216 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1191+2685C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515216 | |||||||
| chr2:9515476 | C | T | 1 | a0001c0001t0009g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1191+2425G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515476 | |||||||
| chr2:9515479 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1191+2422C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515479 | |||||||
| chr2:9515607 | G | A | 2 | a0001c0002t0002g0187 a0001c0002t0002g0202 |
2 | NA19007.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1191+2294C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515607 | |||||||
| chr2:9515695 | T | C | 8 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0039g0054 others(5): Show |
8 | HG00738.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1191+2206A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515695 | |||||||
| chr2:9515715 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+2186G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515715 | |||||||
| chr2:9515735 | C | CA | 14 | a0001c0002t0010g0203 a0002c0003t0025g0061 a0002c0003t0025g0063 others(11): Show |
14 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1191+2165dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515735 | |||||||
| chr2:9515735 | CA | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1191+2165delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9515735 | |||||||
| chr2:9516129 | T | C | 1 | a0002c0003t0040g0059 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1191+1772A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516129 | |||||||
| chr2:9516272 | A | C | 5 | a0001c0001t0011g0110 a0001c0001t0011g0111 a0001c0001t0011g0112 others(2): Show |
5 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191+1629T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516272 | |||||||
| chr2:9516598 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1191+1303G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516598 | |||||||
| chr2:9516613 | C | T | 1 | a0001c0002t0075g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1191+1288G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516613 | |||||||
| chr2:9516630 | G | T | 1 | a0001c0001t0031g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1191+1271C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516630 | |||||||
| chr2:9516652 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1191+1249A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516652 | |||||||
| chr2:9516750 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+1151G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516750 | |||||||
| chr2:9516760 | AT | A | 2 | a0001c0002t0003g0147 a0001c0002t0070g0148 |
2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1191+1140delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516760 | |||||||
| chr2:9516807 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1191+1094C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516807 | |||||||
| chr2:9516995 | G | A | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1191+906C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9516995 | |||||||
| chr2:9517056 | C | A | 1 | a0001c0001t0050g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1191+845G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517056 | |||||||
| chr2:9517183 | G | C | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1191+718C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517183 | |||||||
| chr2:9517484 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1191+417G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517484 | |||||||
| chr2:9517668 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1191+233G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517668 | |||||||
| chr2:9517698 | A | G | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1191+203T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517698 | |||||||
| chr2:9517754 | C | G | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1191+147G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517754 | |||||||
| chr2:9517818 | A | T | 45 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1191+83T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 10/18 | chr2 | 9517818 | |||||||
| chr2:9518259 | C | CA | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.958-13dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518259 | |||||||
| chr2:9518259 | C | CAA | 8 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0009g0139 others(5): Show |
8 | HG00639.hp2 HG00642.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-14_958-13dupTT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518259 | |||||||
| chr2:9518259 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.958-25_958-13delTT others(11): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518259 | |||||||
| chr2:9518393 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.958-146C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518393 | |||||||
| chr2:9518594 | CA | C | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.958-348delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518594 | |||||||
| chr2:9518719 | T | C | 1 | a0001c0001t0028g0081 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.958-472A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518719 | |||||||
| chr2:9518896 | TG | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.958-650delC | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518896 | |||||||
| chr2:9518967 | G | A | 14 | a0001c0001t0017g0048 a0001c0001t0017g0091 a0001c0001t0017g0094 others(11): Show |
14 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.958-720C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9518967 | |||||||
| chr2:9519248 | T | A | 1 | a0001c0001t0004g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.958-1001A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519248 | |||||||
| chr2:9519401 | T | C | 5 | a0001c0001t0011g0110 a0001c0001t0011g0111 a0001c0001t0011g0112 others(2): Show |
5 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.958-1154A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519401 | |||||||
| chr2:9519481 | T | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.958-1234A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519481 | |||||||
| chr2:9519510 | T | G | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.958-1263A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519510 | |||||||
| chr2:9519511 | A | G | 1 | a0001c0002t0006g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.958-1264T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519511 | |||||||
| chr2:9519544 | G | GCTGAATT others(36): Show |
1 | a0001c0002t0010g0188 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.958-1340_958-1298d others(45): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519544 | |||||||
| chr2:9519621 | A | C | 1 | a0001c0001t0013g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.958-1374T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9519621 | |||||||
| chr2:9520635 | T | C | 1 | a0001c0001t0031g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.957+568A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520635 | |||||||
| chr2:9520729 | C | T | 53 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.957+474G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520729 | |||||||
| chr2:9520821 | G | A | 2 | a0001c0001t0001g0007 a0004c0009t0064g0143 |
2 | HG01070.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.957+382C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520821 | |||||||
| chr2:9520919 | A | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+284T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520919 | |||||||
| chr2:9520925 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+278A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520925 | |||||||
| chr2:9520929 | C | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+274G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520929 | |||||||
| chr2:9520938 | A | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+265T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520938 | |||||||
| chr2:9520943 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+260T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520943 | |||||||
| chr2:9520945 | CA | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+257delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520945 | |||||||
| chr2:9520951 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+252A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520951 | |||||||
| chr2:9520954 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+249T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520954 | |||||||
| chr2:9520959 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.957+244A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520959 | |||||||
| chr2:9520964 | C | CA | 9 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(6): Show |
9 | HG00738.hp2 HG01884.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.957+238dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(2): Show |
5 | HG01361.hp1 HG01361.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+234_957+238dup others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAA | 9 | a0001c0001t0017g0048 a0001c0001t0017g0094 a0001c0001t0018g0095 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.957+233_957+238dup others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA | 16 | a0001c0001t0001g0035 a0001c0001t0004g0042 a0001c0001t0004g0084 others(13): Show |
16 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.957+232_957+238dup others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(1): Show |
12 | a0001c0001t0004g0071 a0001c0001t0004g0072 a0001c0001t0004g0074 others(9): Show |
13 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+231_957+238dup others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0018 a0001c0001t0004g0073 a0001c0001t0011g0111 others(2): Show |
5 | HG01346.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+229_957+238dup others(10): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(4): Show |
1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957+228_957+238dup others(11): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0011g0113 a0001c0001t0029g0102 a0001c0006t0001g0004 |
3 | HG00639.hp2 HG02895.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.957+227_957+238dup others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0011 a0001c0001t0011g0114 a0001c0001t0029g0103 others(1): Show |
4 | HG01175.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+226_957+238dup others(13): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(7): Show |
15 | a0001c0001t0001g0003 a0001c0001t0008g0121 a0001c0001t0008g0122 others(12): Show |
15 | HG00642.hp1 HG01070.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.957+225_957+238dup others(14): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(8): Show |
9 | a0001c0001t0001g0027 a0001c0001t0008g0106 a0001c0001t0008g0138 others(6): Show |
9 | HG01071.hp1 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.957+224_957+238dup others(15): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(9): Show |
7 | a0001c0001t0001g0038 a0001c0001t0009g0124 a0001c0001t0012g0115 others(4): Show |
7 | HG01261.hp1 HG01934.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.957+223_957+238dup others(16): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0012g0118 a0001c0001t0024g0028 a0001c0001t0062g0140 |
3 | HG02622.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.957+222_957+238dup others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0008g0119 a0001c0001t0065g0141 |
2 | HG01358.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.957+221_957+238dup others(18): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(12): Show |
1 | a0004c0009t0064g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.957+220_957+238dup others(19): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0002 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.957+217_957+238dup others(22): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(24): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0025 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.957+238_957+239ins others(25): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0014 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.957+238_957+239ins others(28): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0020 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(29): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0007 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(32): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(26): Show |
2 | a0001c0001t0001g0009 a0001c0001t0024g0006 |
2 | HG00099.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.957+238_957+239ins others(33): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0021 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(34): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(28): Show |
1 | a0001c0013t0001g0010 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(35): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0024 a0001c0001t0035g0039 |
2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.957+238_957+239ins others(36): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(30): Show |
2 | a0001c0001t0001g0031 a0005c0007t0023g0008 |
2 | HG02523.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.957+238_957+239ins others(37): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0033 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(38): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.957+238_957+239ins others(39): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(35): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0029 |
2 | HG01517.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.957+238_957+239ins others(42): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(36): Show |
1 | a0001c0001t0001g0022 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.957+238_957+239ins others(43): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(37): Show |
1 | a0001c0001t0033g0023 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(44): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | C | CAAAAAAA others(38): Show |
1 | a0001c0001t0001g0013 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.957+238_957+239ins others(45): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520964 | CA | C | 7 | a0001c0002t0002g0191 a0001c0002t0002g0225 a0001c0002t0005g0151 others(4): Show |
7 | HG00738.hp1 HG01346.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.957+238delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520964 | |||||||
| chr2:9520987 | G | A | 45 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.957+216C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520987 | |||||||
| chr2:9520988 | G | A | 45 | a0001c0001t0004g0042 a0001c0001t0004g0071 a0001c0001t0004g0072 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.957+215C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9520988 | |||||||
| chr2:9521032 | T | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+171A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9521032 | |||||||
| chr2:9521055 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.957+148A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 8/18 | chr2 | 9521055 | |||||||
| chr2:9521380 | G | A | 1 | a0001c0001t0004g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.844-64C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521380 | |||||||
| chr2:9521460 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.844-144G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521460 | |||||||
| chr2:9521500 | T | C | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-184A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521500 | |||||||
| chr2:9521509 | T | C | 1 | a0001c0001t0050g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.844-193A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521509 | |||||||
| chr2:9521614 | T | C | 1 | a0001c0001t0057g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.844-298A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521614 | |||||||
| chr2:9521646 | G | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.844-330C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521646 | |||||||
| chr2:9521672 | G | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-356C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521672 | |||||||
| chr2:9521756 | A | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-440T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521756 | |||||||
| chr2:9521840 | T | TCTGCCTG others(21): Show |
2 | a0001c0001t0004g0083 a0001c0001t0030g0082 |
2 | HG02132.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.844-552_844-525dup others(28): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTGCCTG others(25): Show |
1 | a0001c0001t0004g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.844-525_844-524ins others(32): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTGCCTG others(29): Show |
2 | a0001c0001t0004g0071 a0001c0001t0004g0075 |
2 | HG00597.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.844-525_844-524ins others(36): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTGCCTG others(37): Show |
1 | a0001c0002t0007g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.844-525_844-524ins others(44): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCC | 9 | a0001c0001t0001g0038 a0001c0001t0011g0110 a0001c0001t0011g0113 others(6): Show |
9 | HG00639.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(2): Show |
53 | a0001c0001t0004g0084 a0001c0001t0008g0121 a0001c0001t0011g0111 others(50): Show |
53 | HG00597.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(9): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(6): Show |
1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.844-525_844-524ins others(13): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(10): Show |
7 | a0001c0001t0022g0036 a0001c0001t0022g0037 a0001c0001t0062g0140 others(4): Show |
7 | HG01175.hp2 HG02055.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(18): Show |
1 | a0001c0001t0008g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.844-525_844-524ins others(25): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(22): Show |
15 | a0001c0001t0004g0101 a0001c0001t0008g0122 a0001c0001t0008g0133 others(12): Show |
15 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(29): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(26): Show |
6 | a0001c0001t0008g0106 a0001c0001t0009g0124 a0001c0001t0009g0126 others(3): Show |
6 | HG01099.hp2 HG01106.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.844-525_844-524ins others(33): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(30): Show |
3 | a0001c0001t0009g0137 a0001c0001t0012g0116 a0001c0001t0013g0125 |
3 | HG01074.hp1 HG01934.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.844-525_844-524ins others(37): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(34): Show |
1 | a0001c0001t0008g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.844-525_844-524ins others(41): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCCT others(38): Show |
1 | a0002c0003t0041g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.844-525_844-524ins others(45): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521840 | T | TCTTCCTG others(1): Show |
2 | a0001c0002t0002g0226 a0001c0002t0071g0176 |
2 | HG01952.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.844-525_844-524ins others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521840 | |||||||
| chr2:9521841 | C | CT | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(51): Show |
54 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.844-526dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521841 | |||||||
| chr2:9521843 | G | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(51): Show |
54 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.844-527C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9521843 | |||||||
| chr2:9522081 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.844-765C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522081 | |||||||
| chr2:9522281 | T | C | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-965A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522281 | |||||||
| chr2:9522448 | A | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+801T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522448 | |||||||
| chr2:9522599 | T | C | 1 | a0002c0003t0046g0062 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.843+650A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522599 | |||||||
| chr2:9522691 | T | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.843+558A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522691 | |||||||
| chr2:9522852 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.843+397A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522852 | |||||||
| chr2:9522966 | G | C | 1 | a0001c0008t0073g0180 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.843+283C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9522966 | |||||||
| chr2:9523115 | AT | A | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+133delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 7/18 | chr2 | 9523115 | |||||||
| chr2:9523385 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.754-47A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9523385 | |||||||
| chr2:9523631 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-293G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9523631 | |||||||
| chr2:9523744 | T | C | 48 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(45): Show |
49 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.754-406A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9523744 | |||||||
| chr2:9523746 | G | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-408C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9523746 | |||||||
| chr2:9524035 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.754-697G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524035 | |||||||
| chr2:9524039 | C | CT | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-702dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524039 | |||||||
| chr2:9524053 | T | A | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.754-715A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524053 | |||||||
| chr2:9524170 | A | C | 1 | a0001c0001t0004g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.754-832T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524170 | |||||||
| chr2:9524459 | C | T | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.754-1121G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524459 | |||||||
| chr2:9524464 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.754-1126A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524464 | |||||||
| chr2:9524572 | A | G | 53 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.754-1234T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524572 | |||||||
| chr2:9524917 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.753+1194A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9524917 | |||||||
| chr2:9525013 | CAAAGAAG others(23): Show |
C | 13 | a0001c0001t0017g0048 a0001c0001t0017g0091 a0001c0001t0017g0094 others(10): Show |
13 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.753+1068_753+1097d others(32): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525013 | |||||||
| chr2:9525043 | T | C | 3 | a0001c0001t0022g0036 a0001c0001t0022g0037 a0001c0001t0066g0041 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.753+1068A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525043 | |||||||
| chr2:9525147 | T | C | 1 | a0001c0002t0014g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.753+964A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525147 | |||||||
| chr2:9525172 | G | A | 1 | a0004c0009t0064g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.753+939C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525172 | |||||||
| chr2:9525299 | G | GA | 40 | a0001c0001t0001g0038 a0001c0001t0008g0106 a0001c0001t0011g0110 others(37): Show |
40 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.753+811dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525299 | |||||||
| chr2:9525299 | G | GAA | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.753+810_753+811dup others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525299 | |||||||
| chr2:9525321 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.753+790G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525321 | |||||||
| chr2:9525330 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.753+781T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525330 | |||||||
| chr2:9525405 | T | C | 2 | a0001c0002t0003g0086 a0001c0002t0003g0090 |
2 | HG00099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.753+706A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525405 | |||||||
| chr2:9525416 | C | T | 1 | a0001c0001t0019g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.753+695G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525416 | |||||||
| chr2:9525425 | T | C | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.753+686A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525425 | |||||||
| chr2:9525878 | C | A | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.753+233G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9525878 | |||||||
| chr2:9526071 | A | T | 5 | a0001c0001t0020g0076 a0001c0001t0020g0085 a0001c0001t0020g0100 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+40T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9526071 | |||||||
| chr2:9526072 | T | A | 1 | a0001c0002t0016g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.753+39A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 6/18 | chr2 | 9526072 | |||||||
| chr2:9526396 | G | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.620-152C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9526396 | |||||||
| chr2:9526508 | G | T | 1 | a0001c0002t0021g0224 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.620-264C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9526508 | |||||||
| chr2:9526585 | C | T | 1 | a0001c0001t0004g0072 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.620-341G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9526585 | |||||||
| chr2:9527061 | G | A | 3 | a0001c0002t0005g0151 a0001c0002t0005g0154 a0001c0002t0069g0152 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.619+725C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527061 | |||||||
| chr2:9527283 | C | CAAACA | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.619+498_619+502dup others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527283 | |||||||
| chr2:9527283 | C | CAAACAAA others(8): Show |
7 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.619+488_619+502dup others(15): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527283 | |||||||
| chr2:9527283 | C | CAAAGA | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.619+502_619+503ins others(5): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527283 | |||||||
| chr2:9527306 | A | AC | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.619+479dupG | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527306 | |||||||
| chr2:9527463 | A | G | 14 | a0001c0002t0003g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.619+323T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527463 | |||||||
| chr2:9527622 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.619+164A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527622 | |||||||
| chr2:9527669 | GC | G | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.619+116delG | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527669 | |||||||
| chr2:9527677 | C | T | 1 | a0001c0001t0012g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.619+109G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 5/18 | chr2 | 9527677 | |||||||
| chr2:9528156 | ACT | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-204_451-203del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528156 | |||||||
| chr2:9528290 | T | G | 1 | a0001c0002t0007g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.451-336A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528290 | |||||||
| chr2:9528299 | G | A | 5 | a0001c0001t0011g0110 a0001c0001t0011g0111 a0001c0001t0011g0112 others(2): Show |
5 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-345C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528299 | |||||||
| chr2:9528755 | A | G | 2 | a0001c0001t0022g0036 a0001c0001t0022g0037 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.451-801T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528755 | |||||||
| chr2:9528855 | G | A | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.451-901C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528855 | |||||||
| chr2:9528856 | T | A | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.451-902A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9528856 | |||||||
| chr2:9529173 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.451-1219C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529173 | |||||||
| chr2:9529212 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451-1258C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529212 | |||||||
| chr2:9529215 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.451-1261G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529215 | |||||||
| chr2:9529343 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.451-1389A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529343 | |||||||
| chr2:9529742 | T | C | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.451-1788A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529742 | |||||||
| chr2:9529786 | A | G | 4 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(1): Show |
4 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1832T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529786 | |||||||
| chr2:9529844 | G | A | 9 | a0001c0002t0006g0178 a0001c0002t0006g0216 a0001c0002t0006g0217 others(6): Show |
9 | HG01069.hp2 HG01123.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.451-1890C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529844 | |||||||
| chr2:9529969 | T | TAC | 59 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0030 others(56): Show |
60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.451-2017_451-2016d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529969 | |||||||
| chr2:9529969 | T | TACAC | 2 | a0002c0003t0041g0057 a0002c0003t0045g0058 |
2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.451-2019_451-2016d others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529969 | |||||||
| chr2:9529969 | T | TACACACA others(3): Show |
5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-2025_451-2016d others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9529969 | |||||||
| chr2:9530238 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.451-2284A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530238 | |||||||
| chr2:9530387 | C | A | 1 | a0001c0002t0016g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.451-2433G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530387 | |||||||
| chr2:9530398 | A | C | 3 | a0001c0002t0016g0158 a0003c0004t0005g0159 a0003c0004t0016g0160 |
3 | HG02965.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-2444T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530398 | |||||||
| chr2:9530580 | T | C | 1 | a0001c0002t0002g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.451-2626A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530580 | |||||||
| chr2:9530899 | A | T | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.451-2945T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9530899 | |||||||
| chr2:9531083 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.451-3129C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531083 | |||||||
| chr2:9531112 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.451-3158G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531112 | |||||||
| chr2:9531178 | G | A | 1 | a0001c0001t0009g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.451-3224C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531178 | |||||||
| chr2:9531331 | G | T | 1 | a0001c0001t0012g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-3377C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531331 | |||||||
| chr2:9531472 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-3518G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531472 | |||||||
| chr2:9531559 | G | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-3605C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531559 | |||||||
| chr2:9531634 | G | A | 1 | a0001c0001t0020g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.451-3680C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531634 | |||||||
| chr2:9531681 | G | A | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.451-3727C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531681 | |||||||
| chr2:9531948 | C | T | 3 | a0001c0002t0005g0151 a0001c0002t0005g0154 a0001c0002t0069g0152 |
3 | HG02895.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.450+3886G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9531948 | |||||||
| chr2:9532583 | T | C | 18 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(15): Show |
18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+3251A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532583 | |||||||
| chr2:9532618 | T | C | 1 | a0001c0014t0007g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.450+3216A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532618 | |||||||
| chr2:9532638 | A | AT | 42 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0034 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.450+3195dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532638 | |||||||
| chr2:9532638 | A | ATT | 15 | a0001c0001t0008g0121 a0001c0001t0008g0123 a0001c0001t0009g0124 others(12): Show |
15 | HG01106.hp1 HG01261.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.450+3194_450+3195d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532638 | |||||||
| chr2:9532638 | AT | A | 30 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0003g0078 others(27): Show |
31 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.450+3195delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532638 | |||||||
| chr2:9532676 | C | T | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.450+3158G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532676 | |||||||
| chr2:9532752 | T | C | 1 | a0002c0003t0044g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.450+3082A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9532752 | |||||||
| chr2:9533021 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+2813A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533021 | |||||||
| chr2:9533143 | C | T | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.450+2691G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533143 | |||||||
| chr2:9533150 | T | C | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.450+2684A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533150 | |||||||
| chr2:9533243 | T | A | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+2591A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533243 | |||||||
| chr2:9533330 | T | C | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+2504A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533330 | |||||||
| chr2:9533364 | T | C | 3 | a0001c0002t0002g0226 a0001c0002t0010g0183 a0001c0002t0010g0227 |
3 | HG00621.hp1 HG02071.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.450+2470A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533364 | |||||||
| chr2:9533375 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+2459A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533375 | |||||||
| chr2:9533378 | C | A | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.450+2456G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533378 | |||||||
| chr2:9533396 | A | C | 1 | a0001c0002t0010g0188 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.450+2438T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533396 | |||||||
| chr2:9533418 | G | A | 1 | a0001c0002t0071g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.450+2416C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533418 | |||||||
| chr2:9533478 | CAG | C | 2 | a0001c0001t0031g0108 a0001c0001t0031g0109 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.450+2354_450+2355d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533478 | |||||||
| chr2:9533495 | T | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.450+2339A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533495 | |||||||
| chr2:9533715 | T | C | 1 | a0001c0001t0054g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.450+2119A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533715 | |||||||
| chr2:9533787 | G | A | 2 | a0001c0002t0015g0172 a0001c0002t0015g0173 |
2 | NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.450+2047C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533787 | |||||||
| chr2:9533867 | G | C | 4 | a0001c0002t0002g0205 a0001c0002t0007g0223 a0001c0002t0010g0222 others(1): Show |
4 | HG01358.hp1 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1967C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533867 | |||||||
| chr2:9533918 | C | G | 2 | a0001c0002t0002g0179 a0001c0002t0003g0170 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.450+1916G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9533918 | |||||||
| chr2:9534107 | C | T | 1 | a0001c0002t0021g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.450+1727G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534107 | |||||||
| chr2:9534282 | C | T | 1 | a0001c0001t0011g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.450+1552G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534282 | |||||||
| chr2:9534283 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+1551G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534283 | |||||||
| chr2:9534553 | C | A | 2 | a0001c0001t0017g0091 a0001c0001t0027g0098 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.450+1281G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534553 | |||||||
| chr2:9534557 | C | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.450+1277G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534557 | |||||||
| chr2:9534621 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+1213A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534621 | |||||||
| chr2:9534650 | G | A | 1 | a0001c0002t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.450+1184C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534650 | |||||||
| chr2:9534680 | T | C | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+1154A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534680 | |||||||
| chr2:9534723 | T | G | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+1111A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534723 | |||||||
| chr2:9534771 | C | G | 1 | a0001c0002t0010g0188 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.450+1063G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534771 | |||||||
| chr2:9534934 | A | G | 1 | a0002c0003t0063g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.450+900T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9534934 | |||||||
| chr2:9535099 | T | C | 1 | a0001c0002t0015g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.450+735A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9535099 | |||||||
| chr2:9535342 | T | C | 1 | a0007c0010t0037g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.450+492A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9535342 | |||||||
| chr2:9535360 | G | C | 2 | a0001c0002t0005g0164 a0001c0002t0014g0163 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.450+474C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9535360 | |||||||
| chr2:9535389 | A | G | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+445T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 4/18 | chr2 | 9535389 | |||||||
| chr2:9536041 | T | C | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.362-119A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/18 | chr2 | 9536041 | |||||||
| chr2:9536216 | G | C | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.362-294C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/18 | chr2 | 9536216 | |||||||
| chr2:9536284 | T | C | 25 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(22): Show |
25 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.362-362A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/18 | chr2 | 9536284 | |||||||
| chr2:9536681 | A | G | 1 | a0002c0003t0063g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.361+17T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 3/18 | chr2 | 9536681 | |||||||
| chr2:9536920 | T | G | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.231-92A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9536920 | |||||||
| chr2:9537027 | C | T | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-199G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537027 | |||||||
| chr2:9537109 | T | A | 1 | a0001c0001t0004g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.231-281A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537109 | |||||||
| chr2:9537285 | C | G | 3 | a0001c0001t0022g0036 a0001c0001t0022g0037 a0001c0001t0066g0041 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.231-457G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537285 | |||||||
| chr2:9537455 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.231-627G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537455 | |||||||
| chr2:9537663 | C | T | 1 | a0001c0001t0004g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.231-835G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537663 | |||||||
| chr2:9537668 | C | A | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-840G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537668 | |||||||
| chr2:9537680 | C | T | 1 | a0001c0002t0003g0169 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.231-852G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537680 | |||||||
| chr2:9537876 | A | AGAGGG | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(69): Show |
72 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.231-1053_231-1049d others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537876 | |||||||
| chr2:9537876 | A | AGAGGGGA others(3): Show |
1 | a0001c0001t0024g0006 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.231-1058_231-1049d others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537876 | |||||||
| chr2:9537876 | A | AGAGGGGA others(8): Show |
1 | a0001c0001t0053g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.231-1063_231-1049d others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537876 | |||||||
| chr2:9537876 | A | AGAGGGGA others(13): Show |
5 | a0001c0001t0001g0011 a0001c0001t0019g0043 a0001c0001t0019g0044 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-1068_231-1049d others(22): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537876 | |||||||
| chr2:9537906 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02135.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.231-1078T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537906 | |||||||
| chr2:9537920 | G | A | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.231-1092C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537920 | |||||||
| chr2:9537934 | G | A | 1 | a0001c0002t0021g0224 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.231-1106C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537934 | |||||||
| chr2:9537945 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | HG02135.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.231-1117T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537945 | |||||||
| chr2:9537949 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0002c0003t0025g0061 others(12): Show |
15 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.231-1121C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537949 | |||||||
| chr2:9537949 | GGA | G | 45 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.231-1123_231-1122d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537949 | |||||||
| chr2:9537961 | G | GAGGGGAA others(4): Show |
2 | a0002c0003t0038g0056 a0007c0010t0037g0053 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.231-1144_231-1134d others(13): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537961 | |||||||
| chr2:9537972 | A | AAGGGGAA others(3): Show |
1 | a0001c0002t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.231-1154_231-1145d others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537972 | |||||||
| chr2:9537972 | A | AAGGGGAA others(18): Show |
1 | a0001c0002t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.231-1169_231-1145d others(27): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9537972 | |||||||
| chr2:9538007 | G | GAGGGGAA others(8): Show |
1 | a0002c0003t0038g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.231-1180_231-1179i others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538007 | |||||||
| chr2:9538016 | A | AGAGGGAA others(8): Show |
12 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0039g0054 others(9): Show |
12 | HG00738.hp2 HG01109.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.231-1189_231-1188i others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | |||||||
| chr2:9538016 | A | AGAGGGGA others(8): Show |
123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.231-1189_231-1188i others(17): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | |||||||
| chr2:9538016 | A | AGAGGGGA others(18): Show |
5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.231-1189_231-1188i others(27): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | |||||||
| chr2:9538016 | A | AGAGGGGA others(9): Show |
1 | a0001c0001t0013g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.231-1189_231-1188i others(18): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | |||||||
| chr2:9538016 | A | G | 1 | a0002c0003t0038g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.231-1188T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538016 | |||||||
| chr2:9538119 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.231-1291T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538119 | |||||||
| chr2:9538491 | T | C | 1 | a0001c0002t0003g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.231-1663A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538491 | |||||||
| chr2:9538816 | A | T | 2 | a0001c0001t0029g0102 a0001c0001t0029g0103 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.231-1988T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538816 | |||||||
| chr2:9538820 | C | T | 2 | a0001c0001t0029g0102 a0001c0001t0029g0103 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.231-1992G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538820 | |||||||
| chr2:9538832 | ATCTT | A | 3 | a0001c0002t0016g0158 a0003c0004t0005g0159 a0003c0004t0016g0160 |
3 | HG02965.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.231-2008_231-2005d others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538832 | |||||||
| chr2:9538936 | G | C | 1 | a0007c0010t0037g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.231-2108C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9538936 | |||||||
| chr2:9539083 | G | A | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.231-2255C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539083 | |||||||
| chr2:9539110 | A | AT | 25 | a0001c0001t0001g0034 a0001c0001t0008g0123 a0001c0001t0017g0091 others(22): Show |
25 | HG00738.hp2 HG01109.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.231-2283dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539110 | |||||||
| chr2:9539169 | G | A | 1 | a0001c0002t0071g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.231-2341C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539169 | |||||||
| chr2:9539227 | C | A | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.231-2399G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539227 | |||||||
| chr2:9539352 | T | C | 1 | a0001c0002t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.231-2524A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539352 | |||||||
| chr2:9539400 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.231-2572A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539400 | |||||||
| chr2:9539633 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.231-2805G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539633 | |||||||
| chr2:9539725 | T | C | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.231-2897A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539725 | |||||||
| chr2:9539884 | C | T | 18 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(15): Show |
18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.231-3056G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539884 | |||||||
| chr2:9539980 | A | G | 4 | a0001c0002t0005g0164 a0001c0002t0014g0161 a0001c0002t0014g0162 others(1): Show |
4 | HG02615.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.231-3152T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9539980 | |||||||
| chr2:9540018 | TAC | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.230+3133_230+3134d others(4): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9540018 | |||||||
| chr2:9540046 | C | T | 3 | a0001c0002t0016g0158 a0003c0004t0005g0159 a0003c0004t0016g0160 |
3 | HG02965.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.230+3107G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9540046 | |||||||
| chr2:9540335 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.230+2818G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9540335 | |||||||
| chr2:9540472 | C | G | 1 | a0001c0002t0007g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.230+2681G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9540472 | |||||||
| chr2:9541175 | A | G | 1 | a0001c0001t0008g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.230+1978T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541175 | |||||||
| chr2:9541310 | C | G | 4 | a0001c0001t0012g0115 a0001c0001t0012g0116 a0001c0001t0012g0117 others(1): Show |
4 | HG01934.hp2 HG03225.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+1843G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541310 | |||||||
| chr2:9541456 | G | A | 1 | a0001c0001t0012g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.230+1697C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541456 | |||||||
| chr2:9541556 | C | A | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.230+1597G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541556 | |||||||
| chr2:9541557 | T | A | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.230+1596A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541557 | |||||||
| chr2:9541575 | A | C | 1 | a0001c0001t0057g0070 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.230+1578T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541575 | |||||||
| chr2:9541659 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.230+1494A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541659 | |||||||
| chr2:9541668 | C | A | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.230+1485G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541668 | |||||||
| chr2:9541811 | C | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.230+1342G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9541811 | |||||||
| chr2:9542183 | T | C | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.230+970A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542183 | |||||||
| chr2:9542288 | C | A | 4 | a0001c0001t0026g0066 a0001c0001t0026g0067 a0001c0001t0048g0068 others(1): Show |
4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+865G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542288 | |||||||
| chr2:9542352 | C | T | 4 | a0001c0001t0026g0066 a0001c0001t0026g0067 a0001c0001t0048g0068 others(1): Show |
4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+801G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542352 | |||||||
| chr2:9542355 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(1): Show |
4 | HG02135.hp1 NA19070.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+798G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542355 | |||||||
| chr2:9542496 | C | T | 1 | a0001c0001t0004g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.230+657G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542496 | |||||||
| chr2:9542606 | G | T | 1 | a0002c0003t0038g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.230+547C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542606 | |||||||
| chr2:9542626 | G | A | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.230+527C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542626 | |||||||
| chr2:9542634 | CATT | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.230+516_230+518del others(3): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542634 | |||||||
| chr2:9542775 | G | A | 1 | a0001c0002t0003g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.230+378C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542775 | |||||||
| chr2:9542784 | A | G | 3 | a0001c0002t0016g0158 a0003c0004t0005g0159 a0003c0004t0016g0160 |
3 | HG02965.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.230+369T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542784 | |||||||
| chr2:9542838 | C | T | 4 | a0001c0001t0012g0115 a0001c0001t0012g0116 a0001c0001t0012g0117 others(1): Show |
4 | HG01934.hp2 HG03225.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.230+315G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542838 | |||||||
| chr2:9542956 | C | G | 1 | a0002c0003t0040g0059 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.230+197G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542956 | |||||||
| chr2:9542966 | C | T | 1 | a0001c0002t0010g0183 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.230+187G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542966 | |||||||
| chr2:9542978 | G | A | 1 | a0001c0002t0015g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.230+175C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542978 | |||||||
| chr2:9542989 | C | T | 1 | a0001c0001t0035g0039 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.230+164G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 2/18 | chr2 | 9542989 | |||||||
| chr2:9543567 | T | C | 53 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(50): Show |
54 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.98-282A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9543567 | |||||||
| chr2:9543693 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
49 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.98-408A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9543693 | |||||||
| chr2:9543725 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0013t0001g0010 |
3 | HG00099.hp2 HG01074.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.98-440G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9543725 | |||||||
| chr2:9543731 | G | A | 4 | a0001c0002t0005g0151 a0001c0002t0005g0153 a0001c0002t0005g0154 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-446C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9543731 | |||||||
| chr2:9544040 | A | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-755T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544040 | |||||||
| chr2:9544047 | C | T | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.98-762G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544047 | |||||||
| chr2:9544196 | T | C | 3 | a0001c0001t0011g0110 a0001c0001t0011g0113 a0001c0001t0011g0114 |
3 | HG00639.hp2 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.98-911A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544196 | |||||||
| chr2:9544265 | C | A | 1 | a0004c0009t0064g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.98-980G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544265 | |||||||
| chr2:9544296 | T | G | 1 | a0001c0001t0004g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.98-1011A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544296 | |||||||
| chr2:9544556 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.98-1271C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544556 | |||||||
| chr2:9544857 | T | G | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-1572A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9544857 | |||||||
| chr2:9545386 | T | C | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-2101A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545386 | |||||||
| chr2:9545523 | T | TCA | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-2240_98-2239dup others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545523 | |||||||
| chr2:9545537 | T | C | 1 | a0001c0001t0009g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.98-2252A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545537 | |||||||
| chr2:9545702 | T | C | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-2417A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545702 | |||||||
| chr2:9545788 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-2503G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545788 | |||||||
| chr2:9545821 | C | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.98-2536G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545821 | |||||||
| chr2:9545956 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.98-2671C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545956 | |||||||
| chr2:9545960 | T | C | 4 | a0001c0001t0008g0122 a0001c0001t0008g0133 a0001c0001t0008g0135 others(1): Show |
4 | HG01106.hp1 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-2675A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9545960 | |||||||
| chr2:9546097 | C | CA | 45 | a0001c0001t0003g0078 a0001c0001t0004g0071 a0001c0001t0004g0072 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.98-2813dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546097 | |||||||
| chr2:9546097 | CA | C | 5 | a0001c0001t0019g0043 a0001c0002t0002g0179 a0001c0002t0002g0207 others(2): Show |
5 | HG01517.hp1 HG02523.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-2813delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546097 | |||||||
| chr2:9546153 | T | C | 1 | a0001c0002t0005g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.98-2868A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546153 | |||||||
| chr2:9546311 | A | G | 26 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(23): Show |
26 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.98-3026T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546311 | |||||||
| chr2:9546408 | T | C | 4 | a0001c0001t0026g0066 a0001c0001t0026g0067 a0001c0001t0048g0068 others(1): Show |
4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-3123A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546408 | |||||||
| chr2:9546468 | C | T | 1 | a0001c0001t0066g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.98-3183G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546468 | |||||||
| chr2:9546715 | C | CTTTTTT | 6 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0008g0135 others(3): Show |
6 | HG00280.hp2 HG01070.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3436_98-3431dup others(6): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546715 | |||||||
| chr2:9546715 | C | CTTTTTTT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.98-3437_98-3431dup others(7): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546715 | |||||||
| chr2:9546715 | C | CTTTTTTT others(1): Show |
12 | a0001c0001t0001g0007 a0001c0001t0004g0072 a0001c0001t0008g0122 others(9): Show |
12 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-3438_98-3431dup others(8): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546715 | |||||||
| chr2:9546814 | A | AT | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-3530dupA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546814 | |||||||
| chr2:9546958 | C | T | 1 | a0001c0002t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.98-3673G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9546958 | |||||||
| chr2:9547171 | G | A | 1 | a0001c0002t0021g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.98-3886C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547171 | |||||||
| chr2:9547317 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.98-4032G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547317 | |||||||
| chr2:9547746 | G | T | 1 | a0001c0001t0011g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-4461C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547746 | |||||||
| chr2:9547767 | A | G | 18 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(15): Show |
18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.98-4482T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547767 | |||||||
| chr2:9547806 | T | A | 1 | a0001c0002t0002g0207 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.98-4521A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9547806 | |||||||
| chr2:9548014 | C | T | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.98-4729G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548014 | |||||||
| chr2:9548073 | C | CA | 7 | a0001c0001t0054g0069 a0001c0002t0003g0001 a0001c0002t0003g0086 others(4): Show |
8 | HG00099.hp1 HG00140.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-4789dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548073 | |||||||
| chr2:9548186 | G | C | 13 | a0001c0001t0017g0048 a0001c0001t0017g0091 a0001c0001t0017g0094 others(10): Show |
13 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-4901C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548186 | |||||||
| chr2:9548400 | A | T | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.98-5115T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548400 | |||||||
| chr2:9548538 | C | G | 18 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(15): Show |
18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.98-5253G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548538 | |||||||
| chr2:9548629 | T | C | 1 | a0001c0002t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.98-5344A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548629 | |||||||
| chr2:9548692 | C | G | 13 | a0001c0001t0017g0048 a0001c0001t0017g0091 a0001c0001t0017g0094 others(10): Show |
13 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.98-5407G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548692 | |||||||
| chr2:9548722 | T | C | 1 | a0001c0002t0007g0209 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.98-5437A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548722 | |||||||
| chr2:9548800 | A | G | 1 | a0001c0001t0004g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.98-5515T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9548800 | |||||||
| chr2:9549139 | G | A | 1 | a0002c0003t0063g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.98-5854C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549139 | |||||||
| chr2:9549177 | C | A | 1 | a0001c0002t0010g0227 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.98-5892G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549177 | |||||||
| chr2:9549231 | C | A | 46 | a0001c0001t0003g0078 a0001c0001t0004g0042 a0001c0001t0004g0071 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.98-5946G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549231 | |||||||
| chr2:9549231 | C | T | 1 | a0001c0002t0005g0155 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.98-5946G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549231 | |||||||
| chr2:9549356 | T | C | 6 | a0001c0001t0011g0110 a0001c0001t0011g0111 a0001c0001t0011g0112 others(3): Show |
6 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-6071A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549356 | |||||||
| chr2:9549434 | A | G | 2 | a0001c0001t0031g0108 a0001c0001t0031g0109 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.97+6075T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549434 | |||||||
| chr2:9549809 | G | A | 1 | a0001c0001t0023g0026 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.97+5700C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549809 | |||||||
| chr2:9549948 | G | A | 18 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(15): Show |
18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+5561C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9549948 | |||||||
| chr2:9550014 | A | G | 1 | a0001c0002t0077g0182 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.97+5495T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550014 | |||||||
| chr2:9550085 | C | T | 18 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(15): Show |
18 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+5424G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550085 | |||||||
| chr2:9550162 | G | A | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.97+5347C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550162 | |||||||
| chr2:9550296 | C | A | 1 | a0002c0003t0038g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+5213G>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550296 | |||||||
| chr2:9550439 | CT | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.97+5069delA | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550439 | |||||||
| chr2:9550439 | CTT | C | 60 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0030 others(57): Show |
61 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.97+5068_97+5069del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550439 | |||||||
| chr2:9550439 | CTTT | C | 7 | a0001c0001t0001g0033 a0001c0001t0018g0050 a0001c0001t0060g0087 others(4): Show |
7 | HG00140.hp2 HG01168.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+5067_97+5069del others(3): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550439 | |||||||
| chr2:9550519 | C | G | 1 | a0002c0003t0047g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+4990G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550519 | |||||||
| chr2:9550538 | C | T | 1 | a0002c0003t0043g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.97+4971G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550538 | |||||||
| chr2:9550637 | G | A | 1 | a0001c0001t0008g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.97+4872C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550637 | |||||||
| chr2:9550646 | T | C | 22 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(19): Show |
22 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.97+4863A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550646 | |||||||
| chr2:9550677 | T | A | 8 | a0001c0002t0003g0169 a0001c0002t0003g0170 a0001c0002t0015g0171 others(5): Show |
8 | HG00597.hp2 HG01952.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+4832A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550677 | |||||||
| chr2:9550691 | G | A | 1 | a0001c0002t0071g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.97+4818C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550691 | |||||||
| chr2:9550903 | C | CA | 18 | a0001c0001t0029g0103 a0001c0002t0002g0225 a0001c0002t0006g0178 others(15): Show |
18 | HG01069.hp2 HG01123.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+4605dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550903 | |||||||
| chr2:9550903 | CA | C | 37 | a0001c0001t0001g0034 a0001c0001t0004g0101 a0001c0001t0004g0105 others(34): Show |
37 | HG00642.hp1 HG01109.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.97+4605delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550903 | |||||||
| chr2:9550903 | CAA | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.97+4604_97+4605del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550903 | |||||||
| chr2:9550903 | CAAA | C | 9 | a0001c0001t0001g0003 a0001c0001t0019g0043 a0001c0001t0019g0044 others(6): Show |
9 | HG01074.hp2 HG01175.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+4603_97+4605del others(3): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550903 | |||||||
| chr2:9550936 | G | A | 2 | a0001c0002t0002g0226 a0001c0002t0010g0227 |
2 | HG02071.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.97+4573C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9550936 | |||||||
| chr2:9551010 | G | A | 1 | a0001c0002t0075g0228 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.97+4499C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551010 | |||||||
| chr2:9551072 | C | CA | 12 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(9): Show |
12 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4436dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551072 | |||||||
| chr2:9551088 | G | T | 1 | a0001c0001t0008g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.97+4421C>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551088 | |||||||
| chr2:9551141 | G | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.97+4368C>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551141 | |||||||
| chr2:9551191 | G | A | 22 | a0001c0001t0008g0106 a0001c0001t0008g0119 a0001c0001t0008g0121 others(19): Show |
22 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.97+4318C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551191 | |||||||
| chr2:9551257 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(32): Show |
35 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.97+4252C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551257 | |||||||
| chr2:9551265 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
48 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.97+4244G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551265 | |||||||
| chr2:9551305 | T | C | 1 | a0001c0002t0015g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.97+4204A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551305 | |||||||
| chr2:9551430 | C | T | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+4079G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551430 | |||||||
| chr2:9551461 | A | C | 1 | a0006c0011t0061g0107 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.97+4048T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551461 | |||||||
| chr2:9551618 | C | T | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+3891G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551618 | |||||||
| chr2:9551681 | G | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+3828C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551681 | |||||||
| chr2:9551695 | G | A | 1 | a0002c0003t0038g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+3814C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551695 | |||||||
| chr2:9551786 | T | C | 2 | a0001c0001t0004g0105 a0001c0001t0030g0104 |
2 | HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.97+3723A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551786 | |||||||
| chr2:9551836 | A | G | 4 | a0001c0001t0026g0066 a0001c0001t0026g0067 a0001c0001t0048g0068 others(1): Show |
4 | HG01496.hp1 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+3673T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551836 | |||||||
| chr2:9551923 | G | A | 1 | a0001c0001t0035g0039 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.97+3586C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9551923 | |||||||
| chr2:9552338 | C | T | 1 | a0001c0002t0002g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.97+3171G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552338 | |||||||
| chr2:9552419 | T | G | 3 | a0001c0001t0022g0036 a0001c0001t0022g0037 a0001c0001t0066g0041 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.97+3090A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552419 | |||||||
| chr2:9552536 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.97+2973C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552536 | |||||||
| chr2:9552721 | C | T | 1 | a0001c0001t0008g0106 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.97+2788G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552721 | |||||||
| chr2:9552738 | A | G | 2 | a0001c0002t0002g0179 a0001c0008t0073g0180 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.97+2771T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552738 | |||||||
| chr2:9552786 | T | C | 1 | a0001c0002t0007g0230 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.97+2723A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552786 | |||||||
| chr2:9552894 | G | A | 2 | a0001c0001t0062g0140 a0001c0001t0065g0141 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.97+2615C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552894 | |||||||
| chr2:9552912 | ATT | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+2595_97+2596del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552912 | |||||||
| chr2:9552954 | TA | T | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+2554delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9552954 | |||||||
| chr2:9553001 | T | C | 1 | a0001c0002t0002g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.97+2508A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553001 | |||||||
| chr2:9553025 | G | A | 1 | a0001c0001t0009g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.97+2484C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553025 | |||||||
| chr2:9553353 | G | A | 1 | a0002c0003t0041g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.97+2156C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553353 | |||||||
| chr2:9553376 | T | A | 13 | a0002c0003t0025g0061 a0002c0003t0025g0063 a0002c0003t0038g0056 others(10): Show |
13 | HG00738.hp2 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+2133A>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553376 | |||||||
| chr2:9553607 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.97+1902C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553607 | |||||||
| chr2:9553648 | C | G | 14 | a0001c0002t0003g0147 a0001c0002t0005g0145 a0001c0002t0005g0146 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.97+1861G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553648 | |||||||
| chr2:9553675 | CA | C | 11 | a0001c0001t0001g0038 a0001c0001t0053g0047 a0001c0001t0062g0140 others(8): Show |
11 | HG00738.hp2 HG01256.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+1833delT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553675 | |||||||
| chr2:9553675 | CAA | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(127): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.97+1832_97+1833del others(2): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553675 | |||||||
| chr2:9553683 | AAAAAAAA others(5): Show |
A | 1 | a0002c0003t0063g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.97+1814_97+1825del others(12): Show |
ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553683 | |||||||
| chr2:9553746 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.97+1763C>T | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9553746 | |||||||
| chr2:9554080 | T | TA | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.97+1428dupT | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554080 | |||||||
| chr2:9554166 | C | T | 1 | a0001c0002t0002g0177 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.97+1343G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554166 | |||||||
| chr2:9554195 | T | C | 1 | a0001c0002t0007g0232 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.97+1314A>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554195 | |||||||
| chr2:9554298 | C | G | 5 | a0001c0001t0019g0043 a0001c0001t0019g0044 a0001c0001t0019g0046 others(2): Show |
5 | HG01884.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+1211G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554298 | |||||||
| chr2:9554491 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.97+1018G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554491 | |||||||
| chr2:9554500 | T | G | 1 | a0004c0009t0064g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.97+1009A>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554500 | |||||||
| chr2:9554642 | A | G | 21 | a0001c0001t0017g0048 a0001c0001t0018g0050 a0001c0001t0019g0043 others(18): Show |
21 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.97+867T>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554642 | |||||||
| chr2:9554649 | A | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(31): Show |
34 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+860T>G | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554649 | |||||||
| chr2:9554798 | C | T | 1 | a0001c0001t0004g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.97+711G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9554798 | |||||||
| chr2:9555153 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.97+356G>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9555153 | |||||||
| chr2:9555370 | C | G | 1 | a0001c0001t0001g0002 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.97+139G>C | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9555370 | |||||||
| chr2:9555440 | A | T | 1 | a0001c0001t0066g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.97+69T>A | ADAM17 | ENSG00000151694.15 | transcript | ENST00000310823.8 | protein_coding | 1/18 | chr2 | 9555440 |