Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55504 |
| ensemblid | ENSG00000127863.16 |
| hgncid | 11915 |
| symbol | TNFRSF19 |
| name | TNF receptor superfamily member 19 |
| refseq_nuc | NM_148957.4 |
| refseq_prot | NP_683760.1 |
| ensembl_nuc | ENST00000248484.9 |
| ensembl_prot | ENSP00000248484.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 23570412 |
| end | 23676093 |
| strand | + |
| ver | v1.2 |
| region | chr13:23570412-23676093 |
| region5000 | chr13:23565412-23681093 |
| regionname0 | TNFRSF19_chr13_23570412_23676093 |
| regionname5000 | TNFRSF19_chr13_23565412_23681093 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 417 | 204 | 41 | 31 | 104 | 7 | 20 | 82 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0002 | 0/0 | 417 | 96 | 27 | 18 | 42 | 3 | 6 | 35 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0003 | 0/0 | 417 | 48 | 7 | 13 | 25 | 0 | 3 | 19 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0004 | 0/0 | 417 | 25 | 12 | 1 | 11 | 0 | 1 | 8 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0005 | 0/0 | 417 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0006 | 0/0 | 417 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0007 | 0/0 | 417 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0008 | 0/0 | 417 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0009 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0010 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| a0011 | 0/1 | 417 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | MALKV others(412): Show |
chr13 | 23565412 | 23681093 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1251 | 155 | 21 | 31 | 83 | 6 | 14 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0001c0004 | 1/0 | 1251 | 36 | 9 | 0 | 20 | 0 | 6 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0001c0007 | 0/0 | 1251 | 7 | 7 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0001c0012 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0001c0013 | 0/0 | 1251 | 2 | 1 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0001c0018 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0001c0022 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0002c0002 | 0/0 | 1251 | 59 | 18 | 14 | 20 | 2 | 5 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0002c0005 | 0/0 | 1251 | 34 | 6 | 4 | 22 | 1 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0002c0010 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0002c0017 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0003c0003 | 0/0 | 1251 | 47 | 6 | 13 | 25 | 0 | 3 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0003c0021 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0004c0006 | 0/0 | 1251 | 24 | 11 | 1 | 11 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0004c0016 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0005c0008 | 0/0 | 1251 | 5 | 4 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0006c0009 | 0/0 | 1251 | 3 | 1 | 1 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0007c0011 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0008c0014 | 0/0 | 1251 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0009c0019 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0010c0020 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 | ||
| a0011c0015 | 0/1 | 1251 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ATGGC others(1246): Show |
chr13 | 23565412 | 23681093 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4438 | 82 | 12 | 18 | 37 | 5 | 10 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0002 | 0/0 | 4438 | 2 | 0 | 1 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0003 | 0/0 | 4438 | 22 | 1 | 8 | 9 | 1 | 3 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0004 | 0/0 | 4438 | 26 | 0 | 0 | 26 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0006 | 0/0 | 4438 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0008 | 0/0 | 4438 | 6 | 0 | 0 | 6 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0010 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0013 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0019 | 0/0 | 4438 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0020 | 0/0 | 4407 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4402): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0027 | 0/0 | 4438 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0029 | 0/0 | 4438 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0031 | 0/0 | 4438 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0033 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0034 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0035 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0040 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0041 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0001t0043 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4437): Show |
chr13 | 23565412 | 23681093 |
| a0001c0004t0002 | 1/0 | 4438 | 29 | 5 | 0 | 17 | 0 | 6 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0004t0017 | 0/0 | 4438 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0004t0024 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0004t0025 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0004t0036 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0004t0042 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4437): Show |
chr13 | 23565412 | 23681093 |
| a0001c0007t0001 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0007t0011 | 0/0 | 4438 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0007t0028 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0007t0030 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0012t0001 | 0/0 | 4438 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0013t0003 | 0/0 | 4438 | 2 | 1 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0018t0004 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0001c0022t0016 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0001 | 0/0 | 4438 | 23 | 5 | 8 | 5 | 2 | 3 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0002 | 0/0 | 4438 | 2 | 0 | 1 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0003 | 0/0 | 4438 | 7 | 1 | 1 | 3 | 0 | 2 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0005 | 0/0 | 4437 | 9 | 0 | 2 | 7 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4432): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0006 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0008 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0009 | 0/0 | 4437 | 3 | 0 | 1 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4432): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0010 | 0/0 | 4438 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0013 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0015 | 0/0 | 4438 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0016 | 0/0 | 4438 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0023 | 0/0 | 4437 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4432): Show |
chr13 | 23565412 | 23681093 |
| a0002c0002t0026 | 0/0 | 4438 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0005t0002 | 0/0 | 4438 | 15 | 0 | 2 | 12 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0005t0005 | 0/0 | 4437 | 10 | 0 | 0 | 9 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4432): Show |
chr13 | 23565412 | 23681093 |
| a0002c0005t0012 | 0/0 | 4438 | 5 | 3 | 2 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0005t0014 | 0/0 | 4438 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0005t0039 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0010t0001 | 0/0 | 4438 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0002c0017t0011 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0003c0003t0001 | 0/0 | 4438 | 37 | 0 | 13 | 21 | 0 | 3 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0003c0003t0006 | 0/0 | 4438 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0003c0003t0018 | 0/0 | 4442 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4437): Show |
chr13 | 23565412 | 23681093 |
| a0003c0003t0022 | 0/0 | 4438 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0003c0003t0037 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0003c0003t0038 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0003c0021t0001 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0004c0006t0001 | 0/0 | 4438 | 13 | 3 | 0 | 9 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0004c0006t0002 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0004c0006t0006 | 0/0 | 4438 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0004c0006t0009 | 0/0 | 4437 | 3 | 0 | 1 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4432): Show |
chr13 | 23565412 | 23681093 |
| a0004c0006t0013 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0004c0006t0021 | 0/0 | 4438 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0004c0006t0032 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0004c0016t0006 | 0/0 | 4438 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0005c0008t0007 | 0/0 | 4438 | 5 | 4 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0006c0009t0007 | 0/0 | 4438 | 3 | 1 | 1 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0007c0011t0004 | 0/0 | 4438 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0008c0014t0003 | 0/0 | 4438 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0009c0019t0001 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0010c0020t0004 | 0/0 | 4438 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| a0011c0015t0001 | 0/1 | 4438 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | ACTAG others(4433): Show |
chr13 | 23565412 | 23681093 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0008g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0013g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0019g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0019g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0020g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0020g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0027g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0029g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0031g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0033g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0034g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0035g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0040g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0041g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0001t0043g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0017g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0017g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0017g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0024g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0025g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0036g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0004t0042g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0007t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0007t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0007t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0007t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0007t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0007t0028g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0007t0030g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0012t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0012t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0013t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0013t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0018t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0001c0022t0016g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0003g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0005g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0009g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0009g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0009g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0013g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0016g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0016g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0023g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0002t0026g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0005g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0012g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0012g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0014g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0014g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0005t0039g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0010t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0010t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0002c0017t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0018g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0018g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0018g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0022g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0037g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0003t0038g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0003c0021t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0009g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0009g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0009g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0013g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0021g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0021g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0006t0032g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0004c0016t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0005c0008t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0005c0008t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0005c0008t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0005c0008t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0005c0008t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0006c0009t0007g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0006c0009t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0007c0011t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0007c0011t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0008c0014t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0008c0014t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0009c0019t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0010c0020t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| a0011c0015t0001g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0006 | c0009 | t0007 | g0007 | EUR | FIN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00280 | hp2 | a0001 | c0013 | t0003 | g0259 | EUR | FIN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0044 | EUR | FIN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00323 | hp2 | a0002 | c0005 | t0002 | g0086 | EUR | FIN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0325 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00423 | hp2 | a0001 | c0004 | t0002 | g0324 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00438 | hp1 | a0004 | c0006 | t0001 | g0103 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00609 | hp1 | a0007 | c0011 | t0004 | g0122 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00621 | hp1 | a0002 | c0005 | t0005 | g0351 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00621 | hp2 | a0001 | c0004 | t0002 | g0209 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0318 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00673 | hp1 | a0001 | c0001 | t0008 | g0287 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0204 | EAS | CHS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG00738 | hp2 | a0002 | c0005 | t0012 | g0014 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0263 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01070 | hp1 | a0006 | c0009 | t0007 | g0007 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0264 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01074 | hp2 | a0002 | c0005 | t0012 | g0015 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01099 | hp1 | a0002 | c0002 | t0009 | g0356 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0312 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0108 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01109 | hp2 | a0002 | c0005 | t0002 | g0087 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01175 | hp1 | a0008 | c0014 | t0003 | g0161 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01243 | hp1 | a0002 | c0002 | t0026 | g0105 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01255 | hp1 | a0002 | c0005 | t0002 | g0085 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0289 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01256 | hp1 | a0003 | c0003 | t0001 | g0230 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0303 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0304 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01361 | hp1 | a0001 | c0001 | t0031 | g0199 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01361 | hp2 | a0001 | c0001 | t0027 | g0223 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01433 | hp2 | a0002 | c0002 | t0005 | g0349 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01496 | hp1 | a0005 | c0008 | t0007 | g0030 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01516 | hp2 | a0008 | c0014 | t0003 | g0156 | EUR | IBS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0246 | EUR | IBS | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01884 | hp1 | a0002 | c0002 | t0003 | g0005 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01884 | hp2 | a0004 | c0006 | t0006 | g0032 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0269 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0266 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01975 | hp1 | a0002 | c0002 | t0005 | g0357 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0311 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0313 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0109 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0296 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG01993 | hp2 | a0003 | c0003 | t0001 | g0251 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0300 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02055 | hp1 | a0001 | c0007 | t0011 | g0193 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02056 | hp1 | a0001 | c0004 | t0017 | g0242 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02080 | hp1 | a0004 | c0006 | t0009 | g0365 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02129 | hp1 | a0004 | c0006 | t0001 | g0102 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02129 | hp2 | a0003 | c0003 | t0038 | g0079 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0083 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02135 | hp1 | a0002 | c0005 | t0002 | g0139 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0284 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0163 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0268 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0040 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02155 | hp1 | a0002 | c0005 | t0002 | g0046 | EAS | CDX | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | CDX | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | CDX | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02165 | hp2 | a0001 | c0004 | t0002 | g0002 | EAS | CDX | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02257 | hp1 | a0002 | c0002 | t0015 | g0031 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02258 | hp1 | a0003 | c0003 | t0006 | g0160 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02258 | hp2 | a0005 | c0008 | t0007 | g0019 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02273 | hp1 | a0004 | c0006 | t0009 | g0355 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0265 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0253 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02280 | hp2 | a0001 | c0007 | t0030 | g0331 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0254 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02451 | hp1 | a0002 | c0005 | t0012 | g0017 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02451 | hp2 | a0001 | c0001 | t0013 | g0343 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | KHV | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02572 | hp1 | a0001 | c0007 | t0011 | g0222 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02572 | hp2 | a0004 | c0006 | t0032 | g0140 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02615 | hp1 | a0004 | c0006 | t0006 | g0027 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02615 | hp2 | a0002 | c0017 | t0011 | g0034 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02622 | hp1 | a0002 | c0002 | t0016 | g0116 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02622 | hp2 | a0006 | c0009 | t0007 | g0333 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02630 | hp1 | a0003 | c0021 | t0001 | g0250 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02630 | hp2 | a0002 | c0002 | t0010 | g0033 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02647 | hp1 | a0001 | c0001 | t0020 | g0332 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02647 | hp2 | a0002 | c0005 | t0012 | g0183 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02717 | hp1 | a0002 | c0002 | t0015 | g0026 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02717 | hp2 | a0001 | c0012 | t0001 | g0097 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02723 | hp1 | a0005 | c0008 | t0007 | g0029 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02809 | hp1 | a0004 | c0016 | t0006 | g0037 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02809 | hp2 | a0001 | c0022 | t0016 | g0326 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02818 | hp1 | a0003 | c0003 | t0006 | g0185 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02818 | hp2 | a0002 | c0005 | t0012 | g0182 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02886 | hp1 | a0003 | c0003 | t0018 | g0180 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02886 | hp2 | a0004 | c0006 | t0021 | g0115 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02896 | hp1 | a0001 | c0004 | t0036 | g0221 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02896 | hp2 | a0002 | c0005 | t0014 | g0145 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02897 | hp2 | a0002 | c0005 | t0014 | g0141 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02970 | hp1 | a0001 | c0004 | t0002 | g0111 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02970 | hp2 | a0002 | c0002 | t0010 | g0013 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02976 | hp1 | a0002 | c0010 | t0001 | g0016 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02976 | hp2 | a0001 | c0004 | t0024 | g0344 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03017 | hp2 | a0001 | c0004 | t0002 | g0215 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0273 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03041 | hp2 | a0002 | c0002 | t0010 | g0018 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03098 | hp2 | a0003 | c0003 | t0018 | g0162 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03130 | hp2 | a0002 | c0002 | t0006 | g0036 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03139 | hp2 | a0001 | c0004 | t0025 | g0345 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03195 | hp2 | a0002 | c0010 | t0001 | g0152 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03209 | hp2 | a0004 | c0006 | t0001 | g0117 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03225 | hp1 | a0001 | c0001 | t0033 | g0190 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03225 | hp2 | a0003 | c0003 | t0006 | g0159 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03239 | hp1 | a0004 | c0006 | t0001 | g0041 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03453 | hp1 | a0001 | c0012 | t0001 | g0096 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03453 | hp2 | a0004 | c0006 | t0021 | g0114 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03486 | hp2 | a0001 | c0007 | t0028 | g0189 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03490 | hp1 | a0001 | c0004 | t0002 | g0279 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0135 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03491 | hp1 | a0001 | c0004 | t0002 | g0089 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0129 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0098 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03516 | hp2 | a0005 | c0008 | t0007 | g0022 | AFR | ESN | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03540 | hp1 | a0003 | c0003 | t0018 | g0179 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03540 | hp2 | a0002 | c0002 | t0015 | g0023 | AFR | GWD | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03579 | hp1 | a0002 | c0005 | t0014 | g0142 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03579 | hp2 | a0001 | c0007 | t0011 | g0165 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0217 | SAS | BEB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03831 | hp2 | a0002 | c0005 | t0005 | g0354 | SAS | BEB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03942 | hp2 | a0001 | c0004 | t0002 | g0173 | SAS | BEB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG04115 | hp1 | a0001 | c0004 | t0002 | g0194 | SAS | STU | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0149 | SAS | STU | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG04199 | hp1 | a0001 | c0001 | t0029 | g0175 | SAS | STU | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0088 | SAS | STU | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0290 | SAS | STU | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0153 | SAS | STU | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0174 | SAS | STU | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG04228 | hp2 | a0001 | c0004 | t0002 | g0218 | SAS | STU | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18522 | hp1 | a0004 | c0006 | t0006 | g0025 | AFR | YRI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0155 | AFR | YRI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | CHB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18612 | hp2 | a0009 | c0019 | t0001 | g0270 | EAS | CHB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18747 | hp1 | a0002 | c0005 | t0002 | g0138 | EAS | CHB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18906 | hp1 | a0001 | c0001 | t0034 | g0154 | AFR | YRI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18906 | hp2 | a0001 | c0004 | t0002 | g0112 | AFR | YRI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18939 | hp1 | a0001 | c0004 | t0017 | g0205 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18942 | hp1 | a0002 | c0005 | t0005 | g0367 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18942 | hp2 | a0001 | c0004 | t0002 | g0213 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18943 | hp1 | a0002 | c0005 | t0005 | g0359 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18944 | hp1 | a0004 | c0006 | t0009 | g0361 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18944 | hp2 | a0001 | c0004 | t0002 | g0274 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18945 | hp2 | a0003 | c0003 | t0001 | g0321 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0307 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18948 | hp2 | a0002 | c0005 | t0002 | g0328 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18950 | hp1 | a0003 | c0003 | t0022 | g0008 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18951 | hp1 | a0004 | c0006 | t0001 | g0006 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18953 | hp2 | a0002 | c0002 | t0005 | g0348 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18954 | hp1 | a0002 | c0005 | t0002 | g0137 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0310 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18959 | hp1 | a0001 | c0001 | t0040 | g0090 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18962 | hp1 | a0002 | c0002 | t0009 | g0360 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18964 | hp1 | a0002 | c0005 | t0002 | g0126 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18966 | hp2 | a0002 | c0005 | t0002 | g0100 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18967 | hp1 | a0002 | c0002 | t0005 | g0373 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18970 | hp1 | a0003 | c0003 | t0001 | g0306 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18972 | hp1 | a0002 | c0002 | t0005 | g0347 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18972 | hp2 | a0003 | c0003 | t0001 | g0267 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18973 | hp1 | a0001 | c0004 | t0002 | g0058 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0197 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18978 | hp1 | a0004 | c0006 | t0001 | g0104 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18978 | hp2 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18979 | hp1 | a0002 | c0002 | t0005 | g0353 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18979 | hp2 | a0002 | c0005 | t0002 | g0119 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18981 | hp1 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18981 | hp2 | a0002 | c0005 | t0005 | g0362 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18982 | hp2 | a0002 | c0005 | t0005 | g0363 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18984 | hp1 | a0004 | c0006 | t0001 | g0132 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18985 | hp1 | a0002 | c0005 | t0039 | g0125 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18985 | hp2 | a0002 | c0002 | t0005 | g0358 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18986 | hp2 | a0003 | c0003 | t0037 | g0192 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18987 | hp1 | a0001 | c0004 | t0002 | g0285 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18987 | hp2 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0291 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18990 | hp1 | a0001 | c0004 | t0002 | g0002 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0243 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18993 | hp2 | a0001 | c0004 | t0002 | g0092 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18994 | hp1 | a0010 | c0020 | t0004 | g0297 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18995 | hp1 | a0002 | c0005 | t0005 | g0352 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18995 | hp2 | a0001 | c0001 | t0041 | g0076 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18999 | hp1 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19000 | hp2 | a0002 | c0002 | t0008 | g0106 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19002 | hp1 | a0002 | c0005 | t0002 | g0099 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19002 | hp2 | a0003 | c0003 | t0022 | g0008 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19003 | hp1 | a0002 | c0002 | t0005 | g0368 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19005 | hp2 | a0004 | c0006 | t0001 | g0006 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19006 | hp1 | a0003 | c0003 | t0001 | g0335 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0235 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19011 | hp2 | a0001 | c0001 | t0019 | g0292 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | LWK | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19030 | hp2 | a0004 | c0006 | t0001 | g0124 | AFR | LWK | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19043 | hp1 | a0001 | c0001 | t0035 | g0298 | AFR | LWK | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19043 | hp2 | a0004 | c0006 | t0013 | g0371 | AFR | LWK | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19054 | hp1 | a0001 | c0004 | t0002 | g0060 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19054 | hp2 | a0002 | c0002 | t0009 | g0364 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19056 | hp2 | a0001 | c0018 | t0004 | g0052 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0305 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19060 | hp2 | a0001 | c0004 | t0002 | g0188 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19063 | hp1 | a0002 | c0005 | t0002 | g0120 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0309 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19065 | hp1 | a0001 | c0004 | t0002 | g0002 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19070 | hp1 | a0002 | c0005 | t0005 | g0346 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19075 | hp2 | a0002 | c0002 | t0003 | g0150 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19076 | hp2 | a0001 | c0001 | t0019 | g0169 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19077 | hp1 | a0001 | c0004 | t0017 | g0240 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19077 | hp2 | a0004 | c0006 | t0001 | g0143 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19081 | hp2 | a0004 | c0006 | t0001 | g0131 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19084 | hp1 | a0004 | c0006 | t0001 | g0130 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19085 | hp1 | a0001 | c0004 | t0002 | g0210 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19085 | hp2 | a0007 | c0011 | t0004 | g0121 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19086 | hp2 | a0002 | c0005 | t0002 | g0136 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0302 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19087 | hp2 | a0001 | c0004 | t0002 | g0211 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19088 | hp1 | a0001 | c0004 | t0002 | g0081 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19088 | hp2 | a0002 | c0002 | t0023 | g0350 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19089 | hp2 | a0002 | c0005 | t0005 | g0369 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19090 | hp1 | a0002 | c0005 | t0002 | g0118 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19090 | hp2 | a0001 | c0004 | t0002 | g0080 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19091 | hp1 | a0002 | c0002 | t0005 | g0370 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19091 | hp2 | a0001 | c0004 | t0002 | g0286 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | YRI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA19240 | hp2 | a0002 | c0002 | t0010 | g0035 | AFR | YRI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA20129 | hp1 | a0002 | c0002 | t0010 | g0020 | AFR | ASW | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA20129 | hp2 | a0001 | c0001 | t0043 | g0178 | AFR | ASW | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0094 | EUR | TSI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02109 | hp1 | a0004 | c0006 | t0002 | g0113 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02109 | hp2 | a0001 | c0007 | t0011 | g0164 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02486 | hp2 | a0002 | c0002 | t0016 | g0039 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02559 | hp1 | a0004 | c0006 | t0001 | g0021 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG02559 | hp2 | a0001 | c0004 | t0042 | g0181 | AFR | ACB | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03471 | hp1 | a0005 | c0008 | t0007 | g0184 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG03471 | hp2 | a0001 | c0001 | t0020 | g0330 | AFR | MSL | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG06807 | hp1 | a0001 | c0013 | t0003 | g0260 | AFR | USA | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| HG06807 | hp2 | a0002 | c0002 | t0013 | g0372 | AFR | USA | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18955 | hp1 | a0002 | c0005 | t0005 | g0366 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | USA | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA20300 | hp2 | a0001 | c0004 | t0002 | g0110 | AFR | USA | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | LWK | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | LWK | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| homoSapiens | chm13v2 | a0011 | c0015 | t0001 | g0171 | REF | REF | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0002 | g0252 | REF | REF | TNFRSF19_chr13_23565412_23681093 | TNFRSF19 | chr13 | 23565412 | 23681093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:23593366 | T | A | 4 | a0002 a0004 a0005 others(1): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
missense_variant | MODERATE | c.91T>A | p.Ser31Thr | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/10 | 562/4438 | 91/1254 | 31/417 | chr13 | 23593366 | |||
| chr13:23659080 | C | T | 1 | a0008 | 2 | HG01175.hp1 HG01516.hp2 |
missense_variant | MODERATE | c.476C>T | p.Ala159Val | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/10 | 947/4438 | 476/1254 | 159/417 | chr13 | 23659080 | |||
| chr13:23668027 | C | T | 2 | a0005 a0006 |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
missense_variant | MODERATE | c.784C>T | p.Pro262Ser | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 8/10 | 1255/4438 | 784/1254 | 262/417 | chr13 | 23668027 | |||
| chr13:23668942 | T | C | 2 | a0007 a0010 |
3 | HG00609.hp1 NA18994.hp1 NA19085.hp2 |
missense_variant | MODERATE | c.1090T>C | p.Ser364Pro | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/10 | 1561/4438 | 1090/1254 | 364/417 | chr13 | 23668942 | |||
| chr13:23668951 | G | C | 1 | a0009 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.1099G>C | p.Glu367Gln | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/10 | 1570/4438 | 1099/1254 | 367/417 | chr13 | 23668951 | |||
| chr13:23669065 | G | A | 3 | a0003 a0004 a0009 |
74 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(71): Show |
missense_variant | MODERATE | c.1213G>A | p.Val405Ile | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/10 | 1684/4438 | 1213/1254 | 405/417 | chr13 | 23669065 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:23626722 | G | A | 1 | a0001c0018 | 1 | NA19056.hp2 | synonymous_variant | LOW | c.375G>A | p.Thr125Thr | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/10 | 846/4438 | 375/1254 | 125/417 | chr13 | 23626722 | |||
| chr13:23659105 | C | T | 1 | a0001c0022 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.501C>T | p.Asp167Asp | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/10 | 972/4438 | 501/1254 | 167/417 | chr13 | 23659105 | |||
| chr13:23660378 | A | G | 14 | a0001c0001 a0001c0007 a0001c0013 others(11): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
synonymous_variant | LOW | c.624A>G | p.Ser208Ser | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/10 | 1095/4438 | 624/1254 | 208/417 | chr13 | 23660378 | |||
| chr13:23668026 | C | T | 1 | a0001c0013 | 2 | HG00280.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.783C>T | p.Ser261Ser | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 8/10 | 1254/4438 | 783/1254 | 261/417 | chr13 | 23668026 | |||
| chr13:23669061 | T | C | 17 | a0001c0001 a0001c0012 a0001c0013 others(14): Show |
309 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(306): Show |
synonymous_variant | LOW | c.1209T>C | p.Gly403Gly | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/10 | 1680/4438 | 1209/1254 | 403/417 | chr13 | 23669061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:23570583 | T | C | 10 | a0001c0001t0013 a0001c0004t0024 a0001c0004t0025 others(7): Show |
31 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-300T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/10 | 19601 | chr13 | 23570583 | ||||||
| chr13:23570630 | C | CATAT | 3 | a0001c0001t0043 a0001c0004t0042 a0003c0003t0018 |
5 | HG02559.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-247_-244dupTATA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/10 | 19544 | INFO_REALIGN_3_PRIME | chr13 | 23570630 | |||||
| chr13:23570672 | AT | A | 5 | a0002c0002t0005 a0002c0002t0009 a0002c0002t0023 others(2): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-209delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/10 | 19510 | INFO_REALIGN_3_PRIME | chr13 | 23570672 | |||||
| chr13:23570832 | A | T | 1 | a0003c0003t0022 | 2 | NA18950.hp1 NA19002.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/10 | 19352 | chr13 | 23570832 | ||||||
| chr13:23673599 | G | A | 1 | a0001c0001t0019 | 2 | NA19011.hp2 NA19076.hp2 |
3_prime_UTR_variant | MODIFIER | c.*219G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 219 | chr13 | 23673599 | ||||||
| chr13:23673665 | G | T | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(11): Show |
74 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 285 | chr13 | 23673665 | ||||||
| chr13:23673719 | A | G | 5 | a0001c0001t0004 a0001c0001t0041 a0001c0018t0004 others(2): Show |
31 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*339A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 339 | chr13 | 23673719 | ||||||
| chr13:23673809 | G | T | 1 | a0002c0005t0039 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*429G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 429 | chr13 | 23673809 | ||||||
| chr13:23673894 | T | A | 1 | a0002c0002t0026 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 514 | chr13 | 23673894 | ||||||
| chr13:23673913 | G | A | 1 | a0001c0001t0027 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*533G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 533 | chr13 | 23673913 | ||||||
| chr13:23674100 | G | A | 3 | a0001c0007t0011 a0001c0007t0028 a0002c0017t0011 |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*720G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 720 | chr13 | 23674100 | ||||||
| chr13:23674154 | A | C | 1 | a0003c0003t0038 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*774A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 774 | chr13 | 23674154 | ||||||
| chr13:23674243 | A | C | 1 | a0003c0003t0037 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*863A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 863 | chr13 | 23674243 | ||||||
| chr13:23674289 | T | C | 2 | a0001c0004t0042 a0002c0005t0014 |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*909T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 909 | chr13 | 23674289 | ||||||
| chr13:23674307 | T | C | 1 | a0002c0002t0015 | 3 | HG02257.hp1 HG02717.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*927T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 927 | chr13 | 23674307 | ||||||
| chr13:23674348 | G | A | 1 | a0001c0001t0029 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 968 | chr13 | 23674348 | ||||||
| chr13:23674374 | A | T | 2 | a0005c0008t0007 a0006c0009t0007 |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*994A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 994 | chr13 | 23674374 | ||||||
| chr13:23674464 | A | G | 1 | a0004c0006t0021 | 2 | HG02886.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1084A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1084 | chr13 | 23674464 | ||||||
| chr13:23674508 | C | T | 3 | a0001c0004t0025 a0001c0004t0036 a0002c0005t0012 |
7 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1128C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1128 | chr13 | 23674508 | ||||||
| chr13:23674509 | G | A | 1 | a0001c0007t0030 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1129G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1129 | chr13 | 23674509 | ||||||
| chr13:23674532 | G | C | 1 | a0001c0001t0040 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1152 | chr13 | 23674532 | ||||||
| chr13:23674573 | A | G | 1 | a0001c0001t0035 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1193A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1193 | chr13 | 23674573 | ||||||
| chr13:23674729 | A | G | 2 | a0001c0001t0034 a0002c0002t0015 |
4 | HG02257.hp1 HG02717.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1349A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1349 | chr13 | 23674729 | ||||||
| chr13:23674740 | G | T | 1 | a0001c0004t0017 | 3 | HG02056.hp1 NA18939.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1360G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1360 | chr13 | 23674740 | ||||||
| chr13:23674753 | C | T | 1 | a0001c0001t0041 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1373C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1373 | chr13 | 23674753 | ||||||
| chr13:23674902 | G | A | 3 | a0001c0007t0011 a0001c0007t0028 a0002c0017t0011 |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1522G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1522 | chr13 | 23674902 | ||||||
| chr13:23675068 | G | A | 1 | a0001c0001t0031 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1688G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1688 | chr13 | 23675068 | ||||||
| chr13:23675154 | T | A | 1 | a0001c0007t0030 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1774T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1774 | chr13 | 23675154 | ||||||
| chr13:23675191 | G | C | 1 | a0004c0006t0032 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1811G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1811 | chr13 | 23675191 | ||||||
| chr13:23675250 | CTGTTTGC others(24): Show |
C | 1 | a0001c0001t0020 | 2 | HG02647.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1904_*1934delTTTG others(27): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1904 | INFO_REALIGN_3_PRIME | chr13 | 23675250 | |||||
| chr13:23675349 | G | A | 1 | a0003c0003t0022 | 2 | NA18950.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1969G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1969 | chr13 | 23675349 | ||||||
| chr13:23675379 | T | C | 2 | a0005c0008t0007 a0006c0009t0007 |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1999T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 1999 | chr13 | 23675379 | ||||||
| chr13:23675431 | C | A | 1 | a0001c0007t0028 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2051 | chr13 | 23675431 | ||||||
| chr13:23675439 | A | C | 1 | a0001c0001t0027 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2059A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2059 | chr13 | 23675439 | ||||||
| chr13:23675523 | C | G | 6 | a0001c0001t0006 a0002c0002t0006 a0003c0003t0006 others(3): Show |
12 | HG01109.hp1 HG01884.hp2 HG01981.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2143C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2143 | chr13 | 23675523 | ||||||
| chr13:23675694 | T | C | 2 | a0001c0022t0016 a0002c0002t0016 |
3 | HG02486.hp2 HG02622.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2314T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2314 | chr13 | 23675694 | ||||||
| chr13:23675708 | T | C | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(17): Show |
88 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2328T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2328 | chr13 | 23675708 | ||||||
| chr13:23675711 | C | T | 3 | a0001c0007t0011 a0001c0007t0028 a0002c0017t0011 |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2331C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2331 | chr13 | 23675711 | ||||||
| chr13:23675818 | A | C | 57 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(54): Show |
296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*2438A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2438 | chr13 | 23675818 | ||||||
| chr13:23675952 | A | C | 1 | a0001c0004t0036 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2572A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2572 | chr13 | 23675952 | ||||||
| chr13:23675963 | G | A | 3 | a0001c0007t0011 a0001c0007t0028 a0002c0017t0011 |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2583G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2583 | chr13 | 23675963 | ||||||
| chr13:23676001 | G | T | 1 | a0001c0001t0033 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2621G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 10/10 | 2621 | chr13 | 23676001 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:23570860 | A | G | 1 | a0002c0002t0005g0373 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-35+12A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23570860 | |||||||
| chr13:23570924 | G | C | 33 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(30): Show |
34 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-35+76G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23570924 | |||||||
| chr13:23571023 | T | C | 33 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(30): Show |
34 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-35+175T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23571023 | |||||||
| chr13:23571235 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-35+387T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23571235 | |||||||
| chr13:23571485 | C | T | 31 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 others(28): Show |
31 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.-35+637C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23571485 | |||||||
| chr13:23571540 | A | T | 7 | a0001c0001t0003g0012 a0001c0001t0003g0337 a0001c0001t0003g0338 others(4): Show |
8 | NA18941.hp1 NA18946.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-35+692A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23571540 | |||||||
| chr13:23571709 | A | T | 2 | a0001c0001t0001g0336 a0003c0003t0001g0335 |
2 | NA19006.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-35+861A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23571709 | |||||||
| chr13:23571784 | C | T | 1 | a0001c0001t0001g0334 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-35+936C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23571784 | |||||||
| chr13:23571872 | GT | G | 8 | a0001c0001t0001g0049 a0001c0001t0013g0343 a0001c0004t0024g0344 others(5): Show |
8 | HG02155.hp1 HG02451.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+1035delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23571872 | ||||||
| chr13:23572008 | G | A | 34 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(31): Show |
35 | HG00408.hp2 HG00423.hp1 HG02056.hp2 others(32): Show |
intron_variant | MODIFIER | c.-35+1160G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572008 | |||||||
| chr13:23572170 | A | C | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-35+1322A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572170 | |||||||
| chr13:23572201 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-35+1353G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572201 | |||||||
| chr13:23572282 | A | C | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0001c0007t0030g0331 |
3 | HG02280.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-35+1434A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572282 | |||||||
| chr13:23572338 | T | C | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-35+1490T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572338 | |||||||
| chr13:23572382 | G | A | 26 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(23): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+1534G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572382 | |||||||
| chr13:23572444 | C | A | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-35+1596C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572444 | |||||||
| chr13:23572532 | G | A | 1 | a0002c0005t0005g0346 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-35+1684G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572532 | |||||||
| chr13:23572588 | A | G | 33 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(30): Show |
34 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-35+1740A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572588 | |||||||
| chr13:23572747 | G | A | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-35+1899G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572747 | |||||||
| chr13:23572751 | C | G | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-35+1903C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572751 | |||||||
| chr13:23572841 | C | T | 1 | a0003c0003t0001g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-35+1993C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572841 | |||||||
| chr13:23572846 | C | T | 68 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(65): Show |
72 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-35+1998C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572846 | |||||||
| chr13:23572876 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-35+2028C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572876 | |||||||
| chr13:23572963 | A | G | 26 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(23): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+2115A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23572963 | |||||||
| chr13:23573001 | A | G | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-35+2153A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573001 | |||||||
| chr13:23573014 | G | GATCAC | 3 | a0002c0005t0002g0085 a0002c0005t0002g0086 a0002c0005t0002g0087 |
3 | HG00323.hp2 HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-35+2171_-35+2175d others(7): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23573014 | ||||||
| chr13:23573022 | C | T | 1 | a0001c0001t0004g0329 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-35+2174C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573022 | |||||||
| chr13:23573274 | A | AT | 6 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0001c0004t0036g0221 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+2436dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23573274 | ||||||
| chr13:23573290 | C | A | 26 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(23): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+2442C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573290 | |||||||
| chr13:23573302 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-35+2454G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573302 | |||||||
| chr13:23573390 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0004g0157 |
2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-35+2542A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573390 | |||||||
| chr13:23573481 | G | GCC | 64 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(61): Show |
68 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-35+2634_-35+2635d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23573481 | ||||||
| chr13:23573485 | C | CTG | 37 | a0001c0001t0027g0223 a0001c0004t0036g0221 a0001c0007t0011g0222 others(34): Show |
38 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-35+2649_-35+2650d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23573485 | ||||||
| chr13:23573485 | C | G | 64 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(61): Show |
68 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-35+2637C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573485 | |||||||
| chr13:23573549 | T | C | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01433.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-35+2701T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573549 | |||||||
| chr13:23573552 | A | G | 2 | a0001c0001t0001g0327 a0001c0022t0016g0326 |
2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-35+2704A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573552 | |||||||
| chr13:23573645 | A | C | 1 | a0008c0014t0003g0156 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-35+2797A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573645 | |||||||
| chr13:23573754 | TTTC | T | 51 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(48): Show |
53 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-35+2910_-35+2912d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23573754 | ||||||
| chr13:23573793 | T | C | 2 | a0002c0002t0013g0372 a0004c0006t0013g0371 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+2945T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573793 | |||||||
| chr13:23573919 | G | A | 33 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(30): Show |
34 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-35+3071G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573919 | |||||||
| chr13:23573921 | A | G | 26 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(23): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+3073A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23573921 | |||||||
| chr13:23573998 | CT | C | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-35+3153delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23573998 | ||||||
| chr13:23574010 | C | T | 64 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(61): Show |
68 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-35+3162C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574010 | |||||||
| chr13:23574061 | C | CA | 214 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0077 others(211): Show |
223 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.-35+3233dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23574061 | ||||||
| chr13:23574061 | C | CAA | 39 | a0001c0001t0001g0054 a0001c0001t0001g0166 a0001c0001t0001g0167 others(36): Show |
39 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35+3232_-35+3233d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23574061 | ||||||
| chr13:23574082 | T | C | 9 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0176 others(6): Show |
10 | HG00280.hp1 HG01070.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35+3234T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574082 | |||||||
| chr13:23574110 | T | A | 1 | a0001c0001t0001g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-35+3262T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574110 | |||||||
| chr13:23574125 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0239 |
2 | NA18747.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-35+3277T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574125 | |||||||
| chr13:23574126 | A | G | 31 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 others(28): Show |
31 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.-35+3278A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574126 | |||||||
| chr13:23574149 | GA | G | 55 | a0001c0001t0004g0151 a0002c0002t0001g0098 a0002c0002t0001g0101 others(52): Show |
57 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35+3302delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574149 | |||||||
| chr13:23574184 | G | T | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-35+3336G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574184 | |||||||
| chr13:23574217 | A | G | 1 | a0002c0002t0001g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-35+3369A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574217 | |||||||
| chr13:23574296 | T | C | 26 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(23): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+3448T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574296 | |||||||
| chr13:23574427 | T | C | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0001c0007t0030g0331 |
3 | HG02280.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-35+3579T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574427 | |||||||
| chr13:23574462 | G | GT | 7 | a0001c0001t0043g0178 a0001c0004t0042g0181 a0002c0002t0013g0372 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+3625dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23574462 | ||||||
| chr13:23574462 | G | GTT | 62 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(59): Show |
66 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-35+3624_-35+3625d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23574462 | ||||||
| chr13:23574462 | GT | G | 120 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(117): Show |
124 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-35+3625delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23574462 | ||||||
| chr13:23574611 | T | TC | 7 | a0001c0001t0006g0108 a0001c0001t0006g0109 a0001c0004t0002g0110 others(4): Show |
7 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35+3763_-35+3764i others(3): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574611 | |||||||
| chr13:23574634 | C | G | 1 | a0003c0003t0001g0325 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-35+3786C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574634 | |||||||
| chr13:23574647 | C | T | 2 | a0002c0002t0001g0042 a0004c0006t0001g0041 |
2 | HG03239.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-35+3799C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574647 | |||||||
| chr13:23574717 | T | C | 1 | a0001c0004t0002g0089 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-35+3869T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574717 | |||||||
| chr13:23574779 | G | A | 2 | a0002c0002t0013g0372 a0004c0006t0013g0371 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+3931G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574779 | |||||||
| chr13:23574826 | C | G | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-35+3978C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574826 | |||||||
| chr13:23574851 | C | T | 1 | a0002c0002t0001g0107 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-35+4003C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23574851 | |||||||
| chr13:23575022 | G | C | 2 | a0002c0002t0013g0372 a0004c0006t0013g0371 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+4174G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575022 | |||||||
| chr13:23575139 | G | A | 26 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(23): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+4291G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575139 | |||||||
| chr13:23575164 | A | G | 2 | a0002c0002t0013g0372 a0004c0006t0013g0371 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35+4316A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575164 | |||||||
| chr13:23575347 | G | A | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-35+4499G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575347 | |||||||
| chr13:23575372 | G | C | 1 | a0002c0002t0001g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-35+4524G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575372 | |||||||
| chr13:23575486 | C | A | 4 | a0001c0001t0001g0241 a0001c0004t0017g0240 a0001c0004t0017g0242 others(1): Show |
4 | HG02056.hp1 NA18980.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+4638C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575486 | |||||||
| chr13:23575498 | A | T | 1 | a0001c0004t0002g0324 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-35+4650A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575498 | |||||||
| chr13:23575547 | C | T | 33 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(30): Show |
34 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-35+4699C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575547 | |||||||
| chr13:23575617 | T | C | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-35+4769T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575617 | |||||||
| chr13:23575758 | G | A | 4 | a0002c0002t0005g0357 a0002c0002t0005g0373 a0002c0002t0009g0356 others(1): Show |
4 | HG01099.hp1 HG01975.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+4910G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575758 | |||||||
| chr13:23575997 | A | T | 55 | a0001c0001t0004g0151 a0002c0002t0001g0098 a0002c0002t0001g0101 others(52): Show |
57 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35+5149A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23575997 | |||||||
| chr13:23576136 | C | CT | 7 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0013g0343 others(4): Show |
7 | HG02148.hp2 HG02451.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35+5303dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23576136 | ||||||
| chr13:23576136 | CT | C | 6 | a0001c0001t0010g0155 a0001c0001t0034g0154 a0001c0022t0016g0326 others(3): Show |
6 | HG01169.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35+5303delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23576136 | ||||||
| chr13:23576226 | C | T | 1 | a0002c0002t0003g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-35+5378C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576226 | |||||||
| chr13:23576426 | C | T | 1 | a0001c0004t0002g0218 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-35+5578C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576426 | |||||||
| chr13:23576441 | T | A | 2 | a0001c0004t0036g0221 a0001c0007t0011g0222 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-35+5593T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576441 | |||||||
| chr13:23576492 | C | T | 1 | a0002c0002t0003g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-35+5644C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576492 | |||||||
| chr13:23576510 | C | T | 26 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(23): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+5662C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576510 | |||||||
| chr13:23576940 | G | A | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-35+6092G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576940 | |||||||
| chr13:23576955 | T | C | 2 | a0004c0006t0021g0114 a0004c0006t0021g0115 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-35+6107T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576955 | |||||||
| chr13:23576964 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-35+6116G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576964 | |||||||
| chr13:23576977 | A | G | 1 | a0003c0003t0001g0321 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-35+6129A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23576977 | |||||||
| chr13:23577017 | C | T | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-35+6169C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23577017 | |||||||
| chr13:23577154 | A | G | 1 | a0002c0002t0016g0039 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-35+6306A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23577154 | |||||||
| chr13:23577267 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0314 a0001c0001t0001g0316 others(8): Show |
12 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35+6419C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23577267 | |||||||
| chr13:23577427 | A | G | 1 | a0003c0003t0001g0321 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-35+6579A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23577427 | |||||||
| chr13:23577564 | T | C | 26 | a0002c0002t0005g0347 a0002c0002t0005g0348 a0002c0002t0005g0349 others(23): Show |
26 | HG00621.hp1 HG01099.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35+6716T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23577564 | |||||||
| chr13:23577763 | C | A | 1 | a0003c0003t0001g0230 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-35+6915C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23577763 | |||||||
| chr13:23577788 | G | A | 3 | a0001c0001t0010g0155 a0001c0001t0034g0154 a0004c0006t0002g0113 |
3 | HG02109.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-35+6940G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23577788 | |||||||
| chr13:23577862 | T | C | 3 | a0001c0001t0003g0091 a0001c0001t0040g0090 a0001c0004t0002g0092 |
3 | NA18948.hp1 NA18959.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-35+7014T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23577862 | |||||||
| chr13:23578132 | G | A | 3 | a0002c0005t0012g0182 a0002c0005t0012g0183 a0005c0008t0007g0184 |
3 | HG02647.hp2 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-35+7284G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23578132 | |||||||
| chr13:23578231 | G | C | 68 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(65): Show |
72 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-35+7383G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23578231 | |||||||
| chr13:23578292 | G | C | 58 | a0001c0001t0004g0151 a0002c0002t0001g0098 a0002c0002t0001g0101 others(55): Show |
60 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-35+7444G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23578292 | |||||||
| chr13:23578308 | T | C | 2 | a0002c0002t0001g0042 a0004c0006t0001g0041 |
2 | HG03239.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-35+7460T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23578308 | |||||||
| chr13:23578377 | A | AATG | 58 | a0001c0001t0004g0151 a0002c0002t0001g0098 a0002c0002t0001g0101 others(55): Show |
60 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-35+7531_-35+7532i others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23578377 | ||||||
| chr13:23578447 | C | G | 1 | a0002c0010t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-35+7599C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23578447 | |||||||
| chr13:23578650 | G | A | 58 | a0001c0001t0004g0151 a0002c0002t0001g0098 a0002c0002t0001g0101 others(55): Show |
60 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-35+7802G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23578650 | |||||||
| chr13:23578836 | G | A | 1 | a0001c0001t0003g0311 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-35+7988G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23578836 | |||||||
| chr13:23578887 | G | A | 5 | a0002c0002t0010g0018 a0002c0005t0012g0014 a0002c0005t0012g0015 others(2): Show |
5 | HG00738.hp2 HG01074.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+8039G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23578887 | |||||||
| chr13:23579003 | C | T | 1 | a0003c0003t0001g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-35+8155C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579003 | |||||||
| chr13:23579009 | C | G | 56 | a0001c0001t0004g0151 a0002c0002t0001g0098 a0002c0002t0001g0101 others(53): Show |
58 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-35+8161C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579009 | |||||||
| chr13:23579063 | A | G | 57 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0049 others(54): Show |
58 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-35+8215A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579063 | |||||||
| chr13:23579065 | G | A | 3 | a0002c0005t0012g0182 a0002c0005t0012g0183 a0003c0003t0006g0185 |
3 | HG02647.hp2 HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-35+8217G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579065 | |||||||
| chr13:23579075 | C | G | 7 | a0002c0002t0001g0003 a0002c0002t0001g0038 a0002c0002t0001g0040 others(4): Show |
8 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-35+8227C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579075 | |||||||
| chr13:23579163 | C | T | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0001c0007t0030g0331 |
3 | HG02280.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-35+8315C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579163 | |||||||
| chr13:23579209 | G | A | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-35+8361G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579209 | |||||||
| chr13:23579230 | A | T | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG00639.hp2 HG01106.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-35+8382A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579230 | |||||||
| chr13:23579231 | C | T | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-35+8383C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579231 | |||||||
| chr13:23579243 | TG | T | 28 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(25): Show |
28 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35+8400delG | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23579243 | ||||||
| chr13:23579313 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-35+8465G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579313 | |||||||
| chr13:23579314 | T | G | 59 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(56): Show |
61 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-35+8466T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579314 | |||||||
| chr13:23579380 | C | G | 3 | a0001c0001t0001g0049 a0003c0003t0001g0048 a0003c0003t0001g0050 |
3 | NA18941.hp2 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-35+8532C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579380 | |||||||
| chr13:23579414 | A | C | 1 | a0002c0005t0005g0354 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-35+8566A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579414 | |||||||
| chr13:23579426 | A | AC | 208 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(205): Show |
216 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.-35+8583dupC | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23579426 | ||||||
| chr13:23579476 | C | T | 1 | a0001c0001t0004g0151 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-35+8628C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579476 | |||||||
| chr13:23579493 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-35+8645C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579493 | |||||||
| chr13:23579517 | G | C | 1 | a0002c0002t0005g0358 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-35+8669G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579517 | |||||||
| chr13:23579598 | C | G | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-35+8750C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579598 | |||||||
| chr13:23579604 | G | T | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-35+8756G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579604 | |||||||
| chr13:23579605 | T | G | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-35+8757T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579605 | |||||||
| chr13:23579606 | G | T | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-35+8758G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579606 | |||||||
| chr13:23579627 | C | T | 4 | a0001c0001t0001g0049 a0003c0003t0001g0047 a0003c0003t0001g0048 others(1): Show |
4 | NA18941.hp2 NA18966.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35+8779C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579627 | |||||||
| chr13:23579674 | G | T | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-35+8826G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579674 | |||||||
| chr13:23579770 | C | T | 61 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(58): Show |
65 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-35+8922C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579770 | |||||||
| chr13:23579773 | G | A | 1 | a0001c0001t0006g0108 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-35+8925G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579773 | |||||||
| chr13:23579781 | G | A | 20 | a0002c0002t0001g0024 a0002c0002t0001g0028 a0002c0002t0010g0018 others(17): Show |
20 | HG00738.hp2 HG01074.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35+8933G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579781 | |||||||
| chr13:23579788 | G | A | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0001c0007t0030g0331 |
3 | HG02280.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-35+8940G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579788 | |||||||
| chr13:23579834 | C | A | 9 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0176 others(6): Show |
10 | HG00280.hp1 HG01070.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-35+8986C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579834 | |||||||
| chr13:23579931 | G | A | 28 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(25): Show |
28 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35+9083G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579931 | |||||||
| chr13:23579932 | C | A | 28 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(25): Show |
28 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35+9084C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579932 | |||||||
| chr13:23579952 | G | T | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-35+9104G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23579952 | |||||||
| chr13:23580044 | T | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 others(1): Show |
4 | HG01167.hp2 HG01175.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+9196T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580044 | |||||||
| chr13:23580045 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 others(1): Show |
4 | HG01167.hp2 HG01175.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35+9197C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580045 | |||||||
| chr13:23580167 | G | A | 20 | a0002c0002t0001g0024 a0002c0002t0001g0028 a0002c0002t0010g0018 others(17): Show |
20 | HG00738.hp2 HG01074.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35+9319G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580167 | |||||||
| chr13:23580170 | G | C | 1 | a0002c0010t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-35+9322G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580170 | |||||||
| chr13:23580253 | A | C | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-35+9405A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580253 | |||||||
| chr13:23580320 | AGT | A | 65 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(62): Show |
69 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-35+9475_-35+9476d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23580320 | ||||||
| chr13:23580381 | C | CG | 58 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(55): Show |
60 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-35+9533_-35+9534i others(3): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580381 | |||||||
| chr13:23580381 | C | G | 1 | a0002c0002t0003g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-35+9533C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580381 | |||||||
| chr13:23580604 | G | C | 2 | a0001c0004t0036g0221 a0001c0007t0011g0222 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-34-9546G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580604 | |||||||
| chr13:23580631 | T | G | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0001c0007t0030g0331 |
3 | HG02280.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-34-9519T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580631 | |||||||
| chr13:23580733 | G | C | 5 | a0002c0002t0003g0150 a0002c0005t0002g0099 a0002c0005t0002g0119 others(2): Show |
5 | NA18948.hp2 NA18979.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-9417G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580733 | |||||||
| chr13:23580813 | C | G | 4 | a0001c0001t0006g0108 a0001c0001t0006g0109 a0003c0003t0006g0159 others(1): Show |
4 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34-9337C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580813 | |||||||
| chr13:23580897 | T | C | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-34-9253T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23580897 | |||||||
| chr13:23581000 | T | C | 6 | a0001c0001t0001g0095 a0001c0001t0020g0330 a0001c0001t0020g0332 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-9150T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581000 | |||||||
| chr13:23581066 | T | G | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-34-9084T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581066 | |||||||
| chr13:23581127 | C | CTTT | 4 | a0002c0002t0016g0116 a0004c0006t0001g0117 a0004c0006t0021g0114 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-9021_-34-9019d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23581127 | ||||||
| chr13:23581127 | C | T | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-34-9023C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581127 | |||||||
| chr13:23581128 | T | C | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-34-9022T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581128 | |||||||
| chr13:23581129 | T | TTC | 50 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(47): Show |
52 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-34-9020_-34-9019i others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23581129 | ||||||
| chr13:23581132 | C | CT | 7 | a0001c0001t0010g0155 a0001c0001t0027g0223 a0001c0001t0029g0175 others(4): Show |
7 | HG01361.hp2 HG03831.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-9005dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23581132 | ||||||
| chr13:23581132 | C | CTT | 50 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(47): Show |
52 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34-9006_-34-9005d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23581132 | ||||||
| chr13:23581132 | C | T | 96 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(93): Show |
98 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-34-9018C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581132 | |||||||
| chr13:23581133 | T | C | 1 | a0003c0003t0001g0235 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-34-9017T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581133 | |||||||
| chr13:23581159 | G | A | 1 | a0005c0008t0007g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34-8991G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581159 | |||||||
| chr13:23581239 | G | A | 3 | a0002c0002t0001g0003 a0002c0002t0001g0043 a0002c0002t0001g0044 |
4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-8911G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581239 | |||||||
| chr13:23581307 | G | A | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-34-8843G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581307 | |||||||
| chr13:23581388 | C | T | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-34-8762C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581388 | |||||||
| chr13:23581389 | G | A | 38 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(35): Show |
39 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.-34-8761G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581389 | |||||||
| chr13:23581493 | A | C | 2 | a0001c0001t0001g0214 a0001c0004t0002g0215 |
2 | HG03017.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-34-8657A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581493 | |||||||
| chr13:23581579 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 others(1): Show |
4 | HG01167.hp2 HG01175.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-8571A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581579 | |||||||
| chr13:23581652 | G | A | 28 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(25): Show |
28 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-34-8498G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581652 | |||||||
| chr13:23581776 | A | G | 65 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(62): Show |
69 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-34-8374A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23581776 | |||||||
| chr13:23582009 | A | G | 1 | a0001c0001t0020g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-34-8141A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582009 | |||||||
| chr13:23582013 | G | C | 2 | a0007c0011t0004g0121 a0007c0011t0004g0122 |
2 | HG00609.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-34-8137G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582013 | |||||||
| chr13:23582049 | G | T | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-34-8101G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582049 | |||||||
| chr13:23582058 | A | T | 1 | a0001c0004t0002g0213 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-34-8092A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582058 | |||||||
| chr13:23582155 | C | T | 42 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0237 others(39): Show |
42 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-34-7995C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582155 | |||||||
| chr13:23582196 | T | C | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-7954T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582196 | |||||||
| chr13:23582224 | CA | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0049 others(150): Show |
161 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-34-7899delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582224 | ||||||
| chr13:23582224 | CAA | C | 29 | a0001c0001t0001g0095 a0001c0001t0003g0091 a0001c0001t0004g0051 others(26): Show |
29 | HG01074.hp2 HG01496.hp1 HG02056.hp2 others(26): Show |
intron_variant | MODIFIER | c.-34-7900_-34-7899d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582224 | ||||||
| chr13:23582224 | CAAA | C | 64 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(61): Show |
66 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-34-7901_-34-7899d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582224 | ||||||
| chr13:23582224 | CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0001g0234 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | NA18959.hp2 NA18967.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-7908_-34-7899d others(12): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582224 | ||||||
| chr13:23582224 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0336 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-34-7909_-34-7899d others(13): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582224 | ||||||
| chr13:23582224 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0278 |
3 | HG01346.hp2 HG02683.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-34-7910_-34-7899d others(14): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582224 | ||||||
| chr13:23582224 | CAAAAAAA others(6): Show |
C | 62 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(59): Show |
66 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-34-7911_-34-7899d others(15): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582224 | ||||||
| chr13:23582224 | CAAAAAAA others(7): Show |
C | 8 | a0001c0004t0002g0213 a0002c0002t0006g0036 a0002c0002t0010g0013 others(5): Show |
8 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-7912_-34-7899d others(16): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582224 | ||||||
| chr13:23582305 | G | A | 7 | a0001c0001t0001g0095 a0001c0001t0006g0108 a0001c0001t0006g0109 others(4): Show |
7 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34-7845G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582305 | |||||||
| chr13:23582349 | T | C | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-34-7801T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582349 | |||||||
| chr13:23582375 | T | A | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-34-7775T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582375 | |||||||
| chr13:23582400 | C | CA | 8 | a0001c0001t0003g0311 a0001c0001t0004g0055 a0001c0004t0002g0058 others(5): Show |
8 | HG01243.hp1 HG01975.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-7739dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23582400 | ||||||
| chr13:23582409 | A | T | 1 | a0003c0003t0001g0291 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-34-7741A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582409 | |||||||
| chr13:23582412 | T | A | 1 | a0001c0004t0036g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-34-7738T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582412 | |||||||
| chr13:23582432 | A | G | 1 | a0003c0003t0006g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-34-7718A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582432 | |||||||
| chr13:23582439 | A | G | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-34-7711A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582439 | |||||||
| chr13:23582453 | G | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 others(1): Show |
4 | HG01167.hp2 HG01175.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-7697G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582453 | |||||||
| chr13:23582454 | A | G | 2 | a0001c0001t0010g0155 a0001c0001t0034g0154 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-34-7696A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582454 | |||||||
| chr13:23582626 | G | A | 60 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(57): Show |
62 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-34-7524G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582626 | |||||||
| chr13:23582637 | A | C | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-34-7513A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582637 | |||||||
| chr13:23582738 | G | A | 1 | a0002c0002t0013g0372 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-34-7412G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582738 | |||||||
| chr13:23582798 | A | T | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-34-7352A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582798 | |||||||
| chr13:23582918 | C | G | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-7232C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23582918 | |||||||
| chr13:23583091 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-34-7059A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23583091 | |||||||
| chr13:23583286 | C | G | 2 | a0005c0008t0007g0029 a0005c0008t0007g0030 |
2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-34-6864C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23583286 | |||||||
| chr13:23583312 | C | CA | 6 | a0001c0001t0013g0343 a0001c0004t0002g0188 a0001c0004t0024g0344 others(3): Show |
6 | HG02300.hp1 HG02451.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34-6829dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23583312 | ||||||
| chr13:23583414 | T | G | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-34-6736T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23583414 | |||||||
| chr13:23583421 | T | C | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-34-6729T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23583421 | |||||||
| chr13:23583484 | A | G | 61 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(58): Show |
63 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-34-6666A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23583484 | |||||||
| chr13:23583830 | G | A | 65 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(62): Show |
67 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-34-6320G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23583830 | |||||||
| chr13:23583930 | T | G | 60 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(57): Show |
62 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-34-6220T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23583930 | |||||||
| chr13:23584000 | G | A | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-34-6150G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23584000 | |||||||
| chr13:23584081 | T | G | 2 | a0002c0005t0012g0182 a0002c0005t0012g0183 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-34-6069T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23584081 | |||||||
| chr13:23584128 | G | A | 2 | a0001c0007t0028g0189 a0003c0003t0006g0185 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-34-6022G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23584128 | |||||||
| chr13:23584132 | G | GAGTA | 164 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(161): Show |
169 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-34-6015_-34-6014i others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23584132 | ||||||
| chr13:23584315 | A | G | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-34-5835A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23584315 | |||||||
| chr13:23584357 | C | T | 250 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(247): Show |
259 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.-34-5793C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23584357 | |||||||
| chr13:23584533 | A | C | 164 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(161): Show |
169 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-34-5617A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23584533 | |||||||
| chr13:23584589 | C | A | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34-5561C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23584589 | |||||||
| chr13:23584627 | T | TA | 28 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 others(25): Show |
28 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-34-5505dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23584627 | ||||||
| chr13:23584627 | TA | T | 114 | a0001c0001t0001g0095 a0001c0001t0001g0168 a0001c0001t0001g0241 others(111): Show |
117 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-34-5505delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23584627 | ||||||
| chr13:23584627 | TAA | T | 53 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(50): Show |
55 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-34-5506_-34-5505d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23584627 | ||||||
| chr13:23584803 | G | A | 2 | a0001c0001t0003g0231 a0001c0001t0003g0232 |
2 | HG01099.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-34-5347G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23584803 | |||||||
| chr13:23585067 | AT | A | 59 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(56): Show |
61 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-34-5082delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585067 | |||||||
| chr13:23585158 | T | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 others(1): Show |
4 | HG01167.hp2 HG01175.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34-4992T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585158 | |||||||
| chr13:23585238 | A | G | 3 | a0002c0002t0001g0147 a0002c0002t0001g0148 a0002c0002t0002g0146 |
3 | NA18980.hp2 NA18994.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-34-4912A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585238 | |||||||
| chr13:23585386 | A | G | 229 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(226): Show |
238 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.-34-4764A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585386 | |||||||
| chr13:23585691 | C | T | 1 | a0001c0004t0002g0274 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-34-4459C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585691 | |||||||
| chr13:23585795 | G | C | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-34-4355G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585795 | |||||||
| chr13:23585818 | G | C | 11 | a0001c0001t0001g0237 a0001c0001t0001g0245 a0001c0001t0001g0288 others(8): Show |
11 | HG00673.hp1 HG02135.hp2 NA18973.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34-4332G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585818 | |||||||
| chr13:23585831 | G | A | 9 | a0001c0001t0001g0095 a0001c0001t0006g0108 a0001c0001t0006g0109 others(6): Show |
9 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-4319G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585831 | |||||||
| chr13:23585955 | T | C | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-34-4195T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23585955 | |||||||
| chr13:23586078 | G | A | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-4072G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586078 | |||||||
| chr13:23586115 | G | A | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-4035G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586115 | |||||||
| chr13:23586172 | GGT | G | 38 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(35): Show |
39 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.-34-3974_-34-3973d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23586172 | ||||||
| chr13:23586244 | C | T | 2 | a0002c0005t0005g0362 a0002c0005t0005g0363 |
2 | NA18981.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-34-3906C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586244 | |||||||
| chr13:23586249 | C | A | 1 | a0002c0002t0013g0372 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-34-3901C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586249 | |||||||
| chr13:23586257 | C | CA | 53 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(50): Show |
55 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.-34-3874dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23586257 | ||||||
| chr13:23586257 | C | CAA | 100 | a0001c0001t0002g0059 a0001c0001t0003g0088 a0001c0001t0004g0151 others(97): Show |
103 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-34-3875_-34-3874d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23586257 | ||||||
| chr13:23586257 | CA | C | 42 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(39): Show |
45 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-34-3874delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23586257 | ||||||
| chr13:23586272 | A | AAG | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-34-3877_-34-3876i others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23586272 | ||||||
| chr13:23586633 | T | A | 1 | a0001c0001t0013g0343 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-34-3517T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586633 | |||||||
| chr13:23586716 | G | A | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-34-3434G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586716 | |||||||
| chr13:23586722 | G | C | 1 | a0003c0003t0006g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-34-3428G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586722 | |||||||
| chr13:23586846 | G | A | 1 | a0008c0014t0003g0161 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-34-3304G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586846 | |||||||
| chr13:23586892 | G | A | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-34-3258G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23586892 | |||||||
| chr13:23586980 | AATGC | A | 17 | a0002c0002t0001g0003 a0002c0002t0001g0038 a0002c0002t0001g0040 others(14): Show |
18 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-34-3165_-34-3162d others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23586980 | ||||||
| chr13:23587031 | C | T | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-34-3119C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587031 | |||||||
| chr13:23587044 | A | G | 2 | a0001c0007t0028g0189 a0003c0003t0006g0185 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-34-3106A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587044 | |||||||
| chr13:23587063 | C | T | 2 | a0001c0001t0010g0155 a0001c0001t0034g0154 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-34-3087C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587063 | |||||||
| chr13:23587122 | ACTGAAGC others(27): Show |
A | 1 | a0002c0002t0003g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-34-3026_-34-2993d others(36): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23587122 | ||||||
| chr13:23587133 | TAA | T | 6 | a0001c0001t0043g0178 a0001c0004t0042g0181 a0001c0007t0001g0163 others(3): Show |
6 | HG02145.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-3014_-34-3013d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23587133 | ||||||
| chr13:23587247 | C | T | 2 | a0004c0006t0021g0114 a0004c0006t0021g0115 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-34-2903C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587247 | |||||||
| chr13:23587360 | A | G | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-34-2790A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587360 | |||||||
| chr13:23587372 | C | T | 1 | a0001c0004t0036g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-34-2778C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587372 | |||||||
| chr13:23587407 | G | A | 5 | a0001c0001t0043g0178 a0001c0004t0042g0181 a0003c0003t0018g0162 others(2): Show |
5 | HG02559.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34-2743G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587407 | |||||||
| chr13:23587481 | C | T | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34-2669C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587481 | |||||||
| chr13:23587508 | C | T | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-2642C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587508 | |||||||
| chr13:23587514 | A | G | 65 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(62): Show |
67 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-34-2636A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587514 | |||||||
| chr13:23587568 | GTC | G | 90 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(87): Show |
94 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-34-2577_-34-2576d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23587568 | ||||||
| chr13:23587572 | C | G | 1 | a0001c0001t0003g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-34-2578C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587572 | |||||||
| chr13:23587590 | G | A | 17 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0176 others(14): Show |
18 | HG00280.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-34-2560G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587590 | |||||||
| chr13:23587596 | A | G | 242 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(239): Show |
251 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.-34-2554A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587596 | |||||||
| chr13:23587750 | C | T | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-34-2400C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587750 | |||||||
| chr13:23587842 | A | C | 9 | a0001c0001t0001g0095 a0001c0001t0006g0108 a0001c0001t0006g0109 others(6): Show |
9 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-2308A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587842 | |||||||
| chr13:23587862 | C | T | 242 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(239): Show |
251 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.-34-2288C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587862 | |||||||
| chr13:23587976 | C | T | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-34-2174C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587976 | |||||||
| chr13:23587981 | T | C | 1 | a0003c0003t0001g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-34-2169T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587981 | |||||||
| chr13:23587983 | C | T | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-2167C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23587983 | |||||||
| chr13:23588010 | T | C | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-2140T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588010 | |||||||
| chr13:23588116 | A | T | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34-2034A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588116 | |||||||
| chr13:23588238 | T | C | 139 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(136): Show |
145 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.-34-1912T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588238 | |||||||
| chr13:23588278 | C | G | 1 | a0006c0009t0007g0007 | 2 | HG00280.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.-34-1872C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588278 | |||||||
| chr13:23588290 | C | T | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-34-1860C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588290 | |||||||
| chr13:23588308 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-34-1842C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588308 | |||||||
| chr13:23588736 | C | T | 61 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(58): Show |
65 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-34-1414C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588736 | |||||||
| chr13:23588954 | G | A | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-1196G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588954 | |||||||
| chr13:23588975 | CT | C | 9 | a0002c0002t0001g0107 a0002c0002t0003g0005 a0002c0002t0009g0360 others(6): Show |
10 | HG00438.hp2 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34-1174delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23588975 | |||||||
| chr13:23589078 | T | C | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-1072T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589078 | |||||||
| chr13:23589130 | T | TGGAAACT others(335): Show |
1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34-1004_-34-1003i others(344): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23589130 | ||||||
| chr13:23589181 | T | A | 366 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(363): Show |
381 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(378): Show |
intron_variant | MODIFIER | c.-34-969T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589181 | |||||||
| chr13:23589200 | G | A | 65 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(62): Show |
69 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-34-950G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589200 | |||||||
| chr13:23589324 | T | G | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-826T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589324 | |||||||
| chr13:23589399 | A | G | 1 | a0003c0003t0001g0290 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-34-751A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589399 | |||||||
| chr13:23589427 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-34-723G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589427 | |||||||
| chr13:23589454 | T | A | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-34-696T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589454 | |||||||
| chr13:23589457 | G | C | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-693G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589457 | |||||||
| chr13:23589522 | T | G | 1 | a0003c0003t0001g0335 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-34-628T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589522 | |||||||
| chr13:23589625 | A | G | 1 | a0005c0008t0007g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-34-525A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589625 | |||||||
| chr13:23589678 | T | C | 1 | a0001c0001t0003g0255 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-34-472T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589678 | |||||||
| chr13:23589784 | A | G | 1 | a0004c0006t0001g0143 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-34-366A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589784 | |||||||
| chr13:23589864 | GA | G | 174 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(171): Show |
179 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.-34-284delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 23589864 | ||||||
| chr13:23589938 | T | A | 3 | a0001c0001t0001g0158 a0001c0001t0004g0151 a0001c0001t0004g0157 |
3 | HG02083.hp1 HG02132.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-34-212T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589938 | |||||||
| chr13:23589990 | T | C | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-34-160T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23589990 | |||||||
| chr13:23590002 | C | G | 1 | a0001c0001t0001g0245 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-34-148C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23590002 | |||||||
| chr13:23590064 | A | G | 1 | a0002c0005t0002g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-34-86A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23590064 | |||||||
| chr13:23590065 | T | C | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-34-85T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23590065 | |||||||
| chr13:23590077 | G | A | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-34-73G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 1/9 | chr13 | 23590077 | |||||||
| chr13:23590277 | A | G | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.69+25A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23590277 | |||||||
| chr13:23590361 | G | C | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.69+109G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23590361 | |||||||
| chr13:23590376 | T | C | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.69+124T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23590376 | |||||||
| chr13:23590569 | A | C | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+317A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23590569 | |||||||
| chr13:23590578 | G | A | 106 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(103): Show |
111 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.69+326G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23590578 | |||||||
| chr13:23590844 | T | C | 1 | a0001c0004t0002g0060 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.69+592T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23590844 | |||||||
| chr13:23590953 | A | C | 68 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(65): Show |
72 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.69+701A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23590953 | |||||||
| chr13:23591056 | T | C | 174 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(171): Show |
179 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.69+804T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591056 | |||||||
| chr13:23591077 | T | A | 4 | a0002c0002t0016g0116 a0004c0006t0001g0117 a0004c0006t0021g0114 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+825T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591077 | |||||||
| chr13:23591130 | A | G | 9 | a0001c0001t0001g0095 a0001c0001t0006g0108 a0001c0001t0006g0109 others(6): Show |
9 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+878A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591130 | |||||||
| chr13:23591218 | C | T | 1 | a0004c0016t0006g0037 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.69+966C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591218 | |||||||
| chr13:23591385 | G | A | 3 | a0001c0001t0001g0234 a0003c0003t0006g0159 a0003c0003t0006g0160 |
3 | HG02258.hp1 HG03225.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.69+1133G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591385 | |||||||
| chr13:23591418 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.69+1166A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591418 | |||||||
| chr13:23591476 | T | TA | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.69+1232dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 23591476 | ||||||
| chr13:23591538 | TG | T | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.69+1287delG | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591538 | |||||||
| chr13:23591607 | G | A | 248 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(245): Show |
257 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.69+1355G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591607 | |||||||
| chr13:23591664 | C | T | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.69+1412C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591664 | |||||||
| chr13:23591706 | T | TA | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.69+1459dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 23591706 | ||||||
| chr13:23591712 | TTTTCTTT others(1): Show |
T | 66 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(63): Show |
70 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.69+1472_69+1479del others(8): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 23591712 | ||||||
| chr13:23591728 | C | CT | 40 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(37): Show |
41 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.69+1492dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 23591728 | ||||||
| chr13:23591728 | C | CTT | 61 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(58): Show |
63 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.69+1491_69+1492dup others(2): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 23591728 | ||||||
| chr13:23591728 | CT | C | 23 | a0001c0001t0003g0232 a0002c0002t0002g0312 a0002c0002t0005g0347 others(20): Show |
23 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.69+1492delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 23591728 | ||||||
| chr13:23591732 | T | C | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.69+1480T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591732 | |||||||
| chr13:23591733 | T | C | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.69+1481T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591733 | |||||||
| chr13:23591737 | T | C | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.69+1485T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591737 | |||||||
| chr13:23591790 | A | T | 1 | a0003c0003t0006g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.69+1538A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591790 | |||||||
| chr13:23591820 | G | A | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.70-1525G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591820 | |||||||
| chr13:23591821 | T | G | 174 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(171): Show |
179 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.70-1524T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591821 | |||||||
| chr13:23591892 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.70-1453A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591892 | |||||||
| chr13:23591907 | G | A | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.70-1438G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23591907 | |||||||
| chr13:23592026 | T | C | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.70-1319T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592026 | |||||||
| chr13:23592120 | A | G | 1 | a0002c0005t0005g0369 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.70-1225A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592120 | |||||||
| chr13:23592289 | G | A | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-1056G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592289 | |||||||
| chr13:23592413 | A | T | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.70-932A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592413 | |||||||
| chr13:23592590 | G | C | 37 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(34): Show |
38 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.70-755G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592590 | |||||||
| chr13:23592792 | C | T | 1 | a0006c0009t0007g0007 | 2 | HG00280.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.70-553C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592792 | |||||||
| chr13:23592793 | G | A | 65 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(62): Show |
67 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.70-552G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592793 | |||||||
| chr13:23592813 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.70-532C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592813 | |||||||
| chr13:23592839 | C | T | 1 | a0004c0006t0006g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.70-506C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592839 | |||||||
| chr13:23592883 | T | A | 20 | a0002c0002t0001g0024 a0002c0002t0001g0028 a0002c0002t0010g0018 others(17): Show |
20 | HG00738.hp2 HG01074.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.70-462T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23592883 | |||||||
| chr13:23592986 | G | GT | 69 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(66): Show |
73 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.70-349dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 23592986 | ||||||
| chr13:23592986 | GT | G | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.70-349delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 23592986 | ||||||
| chr13:23593175 | C | T | 1 | a0002c0002t0010g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-170C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23593175 | |||||||
| chr13:23593183 | T | G | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70-162T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23593183 | |||||||
| chr13:23593253 | G | A | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-92G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23593253 | |||||||
| chr13:23593267 | G | T | 4 | a0001c0001t0001g0049 a0003c0003t0001g0047 a0003c0003t0001g0048 others(1): Show |
4 | NA18941.hp2 NA18966.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-78G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23593267 | |||||||
| chr13:23593341 | T | C | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
splice_region_variant&intron_variant | LOW | c.70-4T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 2/9 | chr13 | 23593341 | |||||||
| chr13:23593471 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.180+16G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593471 | |||||||
| chr13:23593687 | T | A | 1 | a0002c0002t0003g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.180+232T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593687 | |||||||
| chr13:23593699 | A | G | 309 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0049 others(306): Show |
319 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.180+244A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593699 | |||||||
| chr13:23593715 | C | T | 65 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(62): Show |
67 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.180+260C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593715 | |||||||
| chr13:23593733 | T | A | 1 | a0002c0002t0003g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.180+278T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593733 | |||||||
| chr13:23593773 | C | T | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+318C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593773 | |||||||
| chr13:23593820 | G | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
6 | HG00735.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+365G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593820 | |||||||
| chr13:23593852 | C | T | 2 | a0005c0008t0007g0029 a0005c0008t0007g0030 |
2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.180+397C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593852 | |||||||
| chr13:23593860 | G | A | 9 | a0002c0002t0001g0107 a0002c0002t0003g0005 a0002c0002t0009g0360 others(6): Show |
10 | HG00438.hp2 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+405G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593860 | |||||||
| chr13:23593938 | C | T | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+483C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593938 | |||||||
| chr13:23593945 | T | G | 1 | a0003c0003t0006g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.180+490T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23593945 | |||||||
| chr13:23594013 | C | T | 174 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(171): Show |
179 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.180+558C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594013 | |||||||
| chr13:23594080 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.180+625C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594080 | |||||||
| chr13:23594199 | C | G | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0001c0007t0030g0331 |
3 | HG02280.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.180+744C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594199 | |||||||
| chr13:23594223 | C | T | 31 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(28): Show |
32 | HG00408.hp2 HG00423.hp1 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.180+768C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594223 | |||||||
| chr13:23594426 | G | A | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+971G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594426 | |||||||
| chr13:23594443 | A | T | 5 | a0002c0005t0014g0141 a0002c0005t0014g0142 a0002c0005t0014g0145 others(2): Show |
5 | HG02572.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+988A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594443 | |||||||
| chr13:23594582 | G | A | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+1127G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594582 | |||||||
| chr13:23594603 | A | G | 68 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(65): Show |
72 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.180+1148A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594603 | |||||||
| chr13:23594696 | C | T | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+1241C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594696 | |||||||
| chr13:23594898 | C | T | 65 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(62): Show |
67 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.180+1443C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594898 | |||||||
| chr13:23594920 | A | G | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+1465A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23594920 | |||||||
| chr13:23595032 | T | A | 1 | a0001c0001t0001g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.180+1577T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595032 | |||||||
| chr13:23595275 | A | G | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+1820A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595275 | |||||||
| chr13:23595306 | G | T | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+1851G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595306 | |||||||
| chr13:23595460 | C | T | 2 | a0001c0001t0001g0327 a0001c0022t0016g0326 |
2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.180+2005C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595460 | |||||||
| chr13:23595549 | A | G | 1 | a0001c0004t0002g0211 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.180+2094A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595549 | |||||||
| chr13:23595568 | T | C | 1 | a0001c0001t0029g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.180+2113T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595568 | |||||||
| chr13:23595653 | C | T | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+2198C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595653 | |||||||
| chr13:23595654 | G | A | 4 | a0001c0001t0006g0108 a0001c0001t0006g0109 a0003c0003t0006g0159 others(1): Show |
4 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+2199G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595654 | |||||||
| chr13:23595681 | A | G | 17 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0176 others(14): Show |
18 | HG00280.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.180+2226A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595681 | |||||||
| chr13:23595710 | T | C | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.180+2255T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23595710 | |||||||
| chr13:23596320 | A | C | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+2865A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23596320 | |||||||
| chr13:23596329 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0033g0190 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.180+2874C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23596329 | |||||||
| chr13:23596377 | G | A | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+2922G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23596377 | |||||||
| chr13:23596508 | A | G | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.180+3053A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23596508 | |||||||
| chr13:23596818 | C | T | 5 | a0001c0001t0001g0166 a0001c0001t0001g0170 a0001c0007t0011g0164 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+3363C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23596818 | |||||||
| chr13:23596858 | T | C | 127 | a0001c0001t0010g0155 a0001c0001t0034g0154 a0002c0002t0001g0003 others(124): Show |
130 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.180+3403T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23596858 | |||||||
| chr13:23596946 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.180+3491A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23596946 | |||||||
| chr13:23596947 | C | T | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.180+3492C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23596947 | |||||||
| chr13:23597086 | A | G | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.180+3631A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597086 | |||||||
| chr13:23597308 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.180+3853C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597308 | |||||||
| chr13:23597343 | C | T | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.180+3888C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597343 | |||||||
| chr13:23597365 | G | T | 1 | a0001c0004t0002g0210 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.180+3910G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597365 | |||||||
| chr13:23597473 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0236 a0001c0001t0001g0314 others(8): Show |
12 | HG00639.hp1 HG01069.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.180+4018A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597473 | |||||||
| chr13:23597524 | A | G | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+4069A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597524 | |||||||
| chr13:23597610 | CT | C | 68 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(65): Show |
72 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.180+4156delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597610 | |||||||
| chr13:23597640 | G | A | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+4185G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597640 | |||||||
| chr13:23597693 | T | C | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+4238T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597693 | |||||||
| chr13:23597740 | C | G | 65 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(62): Show |
69 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.180+4285C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597740 | |||||||
| chr13:23597833 | A | G | 1 | a0002c0002t0003g0005 | 2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.180+4378A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597833 | |||||||
| chr13:23597910 | G | A | 42 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0237 others(39): Show |
42 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.180+4455G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23597910 | |||||||
| chr13:23598073 | T | G | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+4618T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23598073 | |||||||
| chr13:23598196 | G | A | 7 | a0002c0002t0001g0003 a0002c0002t0001g0038 a0002c0002t0001g0040 others(4): Show |
8 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.180+4741G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23598196 | |||||||
| chr13:23598259 | T | A | 1 | a0002c0002t0001g0038 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.180+4804T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23598259 | |||||||
| chr13:23598297 | A | C | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.180+4842A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23598297 | |||||||
| chr13:23598473 | T | C | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.180+5018T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23598473 | |||||||
| chr13:23598584 | T | C | 1 | a0001c0001t0006g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.180+5129T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23598584 | |||||||
| chr13:23598889 | G | A | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.180+5434G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23598889 | |||||||
| chr13:23598910 | T | C | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+5455T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23598910 | |||||||
| chr13:23599029 | T | C | 18 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(15): Show |
19 | HG00642.hp1 HG01516.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.180+5574T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599029 | |||||||
| chr13:23599033 | G | A | 2 | a0002c0002t0010g0020 a0004c0006t0001g0021 |
2 | HG02559.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.180+5578G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599033 | |||||||
| chr13:23599133 | T | C | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+5678T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599133 | |||||||
| chr13:23599339 | A | G | 1 | a0004c0006t0009g0361 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.180+5884A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599339 | |||||||
| chr13:23599458 | C | T | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+6003C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599458 | |||||||
| chr13:23599524 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.180+6069T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599524 | |||||||
| chr13:23599549 | T | C | 103 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(100): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.180+6094T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599549 | |||||||
| chr13:23599801 | G | A | 53 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0062 others(50): Show |
55 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.180+6346G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599801 | |||||||
| chr13:23599829 | C | T | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+6374C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599829 | |||||||
| chr13:23599847 | T | G | 125 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(122): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+6392T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23599847 | |||||||
| chr13:23600242 | A | G | 7 | a0001c0001t0001g0095 a0001c0001t0006g0108 a0001c0001t0006g0109 others(4): Show |
7 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+6787A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23600242 | |||||||
| chr13:23600263 | C | T | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+6808C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23600263 | |||||||
| chr13:23600454 | C | T | 60 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(57): Show |
62 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.180+6999C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23600454 | |||||||
| chr13:23600491 | A | G | 65 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(62): Show |
67 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.180+7036A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23600491 | |||||||
| chr13:23600778 | C | G | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+7323C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23600778 | |||||||
| chr13:23600862 | C | T | 37 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(34): Show |
38 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.180+7407C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23600862 | |||||||
| chr13:23600865 | A | G | 102 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(99): Show |
105 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.180+7410A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23600865 | |||||||
| chr13:23600957 | G | C | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+7502G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23600957 | |||||||
| chr13:23601024 | T | G | 102 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(99): Show |
105 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.180+7569T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601024 | |||||||
| chr13:23601260 | A | G | 65 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(62): Show |
67 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.180+7805A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601260 | |||||||
| chr13:23601281 | T | G | 124 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(121): Show |
127 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.180+7826T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601281 | |||||||
| chr13:23601313 | A | G | 69 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(66): Show |
73 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.180+7858A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601313 | |||||||
| chr13:23601330 | G | T | 124 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(121): Show |
127 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.180+7875G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601330 | |||||||
| chr13:23601424 | T | C | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+7969T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601424 | |||||||
| chr13:23601637 | A | C | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.180+8182A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601637 | |||||||
| chr13:23601642 | A | G | 37 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(34): Show |
38 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.180+8187A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601642 | |||||||
| chr13:23601650 | G | T | 4 | a0001c0004t0002g0002 a0001c0004t0002g0194 a0001c0004t0002g0209 others(1): Show |
6 | HG00621.hp2 HG02165.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+8195G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601650 | |||||||
| chr13:23601669 | TAC | T | 65 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(62): Show |
69 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.180+8230_180+8231d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23601669 | ||||||
| chr13:23601707 | A | T | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+8252A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601707 | |||||||
| chr13:23601797 | A | G | 11 | a0001c0001t0001g0237 a0001c0001t0001g0245 a0001c0001t0001g0288 others(8): Show |
11 | HG00673.hp1 HG02135.hp2 NA18973.hp2 others(8): Show |
intron_variant | MODIFIER | c.180+8342A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601797 | |||||||
| chr13:23601992 | C | T | 2 | a0002c0002t0001g0042 a0004c0006t0001g0041 |
2 | HG03239.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.180+8537C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23601992 | |||||||
| chr13:23602003 | A | G | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.180+8548A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23602003 | |||||||
| chr13:23602080 | C | A | 7 | a0002c0002t0006g0036 a0002c0002t0010g0013 a0002c0002t0010g0033 others(4): Show |
7 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+8625C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23602080 | |||||||
| chr13:23602414 | C | T | 173 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(170): Show |
178 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.180+8959C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23602414 | |||||||
| chr13:23602484 | T | G | 37 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(34): Show |
38 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.180+9029T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23602484 | |||||||
| chr13:23602574 | G | C | 124 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(121): Show |
127 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.180+9119G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23602574 | |||||||
| chr13:23602605 | A | T | 173 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(170): Show |
178 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.180+9150A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23602605 | |||||||
| chr13:23602699 | A | G | 65 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(62): Show |
69 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.180+9244A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23602699 | |||||||
| chr13:23603398 | TGAA | T | 8 | a0002c0002t0001g0101 a0002c0002t0003g0150 a0002c0005t0002g0099 others(5): Show |
8 | NA18948.hp2 NA18964.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.180+9950_180+9952d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23603398 | ||||||
| chr13:23603492 | A | G | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+10037A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23603492 | |||||||
| chr13:23603517 | A | G | 367 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(364): Show |
382 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(379): Show |
intron_variant | MODIFIER | c.180+10062A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23603517 | |||||||
| chr13:23603694 | T | A | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+10239T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23603694 | |||||||
| chr13:23603708 | G | A | 253 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(250): Show |
262 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.180+10253G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23603708 | |||||||
| chr13:23603710 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.180+10255G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23603710 | |||||||
| chr13:23604000 | C | A | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+10545C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604000 | |||||||
| chr13:23604002 | C | T | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.180+10547C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604002 | |||||||
| chr13:23604061 | C | G | 173 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(170): Show |
178 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.180+10606C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604061 | |||||||
| chr13:23604144 | A | G | 1 | a0003c0003t0001g0289 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.180+10689A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604144 | |||||||
| chr13:23604259 | A | AC | 30 | a0001c0001t0001g0191 a0001c0001t0033g0190 a0002c0002t0001g0147 others(27): Show |
30 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.180+10812dupC | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23604259 | ||||||
| chr13:23604259 | A | ACC | 85 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(82): Show |
88 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.180+10811_180+1081 others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23604259 | ||||||
| chr13:23604290 | G | A | 253 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(250): Show |
262 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.180+10835G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604290 | |||||||
| chr13:23604395 | G | T | 173 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(170): Show |
178 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.180+10940G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604395 | |||||||
| chr13:23604679 | G | C | 1 | a0002c0002t0003g0144 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.181-11188G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604679 | |||||||
| chr13:23604798 | T | G | 1 | a0001c0001t0004g0157 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.181-11069T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604798 | |||||||
| chr13:23604863 | G | C | 66 | a0001c0001t0001g0191 a0001c0001t0033g0190 a0002c0002t0001g0098 others(63): Show |
68 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.181-11004G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23604863 | |||||||
| chr13:23605063 | A | G | 9 | a0001c0001t0001g0095 a0001c0001t0006g0108 a0001c0001t0006g0109 others(6): Show |
9 | HG01109.hp1 HG01981.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.181-10804A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605063 | |||||||
| chr13:23605123 | A | G | 2 | a0001c0004t0036g0221 a0001c0007t0011g0222 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.181-10744A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605123 | |||||||
| chr13:23605264 | C | T | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.181-10603C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605264 | |||||||
| chr13:23605314 | T | C | 254 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(251): Show |
263 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.181-10553T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605314 | |||||||
| chr13:23605322 | G | C | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0001c0007t0030g0331 |
3 | HG02280.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.181-10545G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605322 | |||||||
| chr13:23605443 | C | T | 1 | a0002c0002t0015g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.181-10424C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605443 | |||||||
| chr13:23605457 | A | C | 175 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(172): Show |
180 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.181-10410A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605457 | |||||||
| chr13:23605457 | A | G | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.181-10410A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605457 | |||||||
| chr13:23605532 | G | T | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-10335G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605532 | |||||||
| chr13:23605565 | C | A | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.181-10302C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605565 | |||||||
| chr13:23605566 | G | A | 37 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0177 others(34): Show |
40 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.181-10301G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605566 | |||||||
| chr13:23605629 | A | G | 1 | a0001c0004t0002g0274 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.181-10238A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605629 | |||||||
| chr13:23605651 | C | T | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.181-10216C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605651 | |||||||
| chr13:23605808 | G | A | 1 | a0004c0006t0013g0371 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181-10059G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23605808 | |||||||
| chr13:23606051 | G | A | 173 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(170): Show |
178 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.181-9816G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606051 | |||||||
| chr13:23606063 | G | A | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-9804G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606063 | |||||||
| chr13:23606179 | G | A | 59 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(56): Show |
61 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.181-9688G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606179 | |||||||
| chr13:23606309 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0212 |
2 | HG02683.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.181-9558A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606309 | |||||||
| chr13:23606313 | A | G | 9 | a0002c0002t0006g0036 a0002c0002t0010g0013 a0002c0002t0010g0033 others(6): Show |
9 | HG02615.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.181-9554A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606313 | |||||||
| chr13:23606350 | TA | T | 42 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(39): Show |
45 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.181-9515delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23606350 | ||||||
| chr13:23606359 | TA | T | 183 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(180): Show |
189 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.181-9499delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23606359 | ||||||
| chr13:23606360 | A | T | 72 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(69): Show |
75 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.181-9507A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606360 | |||||||
| chr13:23606361 | A | T | 241 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(238): Show |
249 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.181-9506A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606361 | |||||||
| chr13:23606631 | T | A | 4 | a0002c0002t0001g0123 a0002c0002t0001g0244 a0002c0002t0001g0246 others(1): Show |
4 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-9236T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606631 | |||||||
| chr13:23606733 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.181-9134T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606733 | |||||||
| chr13:23606840 | TTTATAAG others(12): Show |
T | 1 | a0001c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.181-9025_181-9007d others(21): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23606840 | ||||||
| chr13:23606883 | A | T | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.181-8984A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23606883 | |||||||
| chr13:23607048 | G | A | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-8819G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607048 | |||||||
| chr13:23607083 | A | AT | 5 | a0001c0001t0043g0178 a0001c0004t0042g0181 a0003c0003t0018g0162 others(2): Show |
5 | HG02559.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-8776dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23607083 | ||||||
| chr13:23607102 | C | T | 67 | a0001c0001t0001g0191 a0001c0001t0033g0190 a0002c0002t0001g0098 others(64): Show |
69 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.181-8765C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607102 | |||||||
| chr13:23607116 | C | CT | 104 | a0001c0001t0001g0191 a0001c0001t0033g0190 a0002c0002t0001g0003 others(101): Show |
107 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.181-8745dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23607116 | ||||||
| chr13:23607218 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0195 |
2 | HG00642.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.181-8649G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607218 | |||||||
| chr13:23607634 | G | T | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.181-8233G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607634 | |||||||
| chr13:23607635 | A | G | 2 | a0001c0001t0010g0155 a0001c0001t0034g0154 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.181-8232A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607635 | |||||||
| chr13:23607663 | A | C | 2 | a0001c0001t0010g0155 a0001c0001t0034g0154 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.181-8204A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607663 | |||||||
| chr13:23607663 | AT | A | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.181-8198delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23607663 | ||||||
| chr13:23607842 | C | T | 1 | a0001c0007t0001g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.181-8025C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607842 | |||||||
| chr13:23607859 | G | A | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.181-8008G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607859 | |||||||
| chr13:23607897 | C | T | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-7970C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607897 | |||||||
| chr13:23607901 | G | A | 4 | a0001c0001t0001g0049 a0003c0003t0001g0047 a0003c0003t0001g0048 others(1): Show |
4 | NA18941.hp2 NA18966.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-7966G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607901 | |||||||
| chr13:23607987 | A | G | 2 | a0002c0002t0010g0020 a0004c0006t0001g0021 |
2 | HG02559.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.181-7880A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23607987 | |||||||
| chr13:23608100 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.181-7767C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608100 | |||||||
| chr13:23608166 | C | T | 1 | a0001c0004t0002g0060 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.181-7701C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608166 | |||||||
| chr13:23608239 | T | C | 253 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(250): Show |
262 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.181-7628T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608239 | |||||||
| chr13:23608240 | G | A | 18 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(15): Show |
19 | HG00642.hp1 HG01516.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.181-7627G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608240 | |||||||
| chr13:23608276 | C | T | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.181-7591C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608276 | |||||||
| chr13:23608310 | G | C | 1 | a0002c0002t0009g0364 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.181-7557G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608310 | |||||||
| chr13:23608360 | A | G | 126 | a0001c0001t0001g0191 a0001c0001t0033g0190 a0002c0002t0001g0003 others(123): Show |
129 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.181-7507A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608360 | |||||||
| chr13:23608411 | A | G | 59 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(56): Show |
63 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.181-7456A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608411 | |||||||
| chr13:23608932 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.181-6935C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608932 | |||||||
| chr13:23608989 | G | A | 1 | a0001c0001t0010g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.181-6878G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608989 | |||||||
| chr13:23608998 | A | T | 1 | a0001c0001t0001g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.181-6869A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23608998 | |||||||
| chr13:23609006 | C | T | 37 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0177 others(34): Show |
40 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.181-6861C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23609006 | |||||||
| chr13:23609218 | A | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01433.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.181-6649A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23609218 | |||||||
| chr13:23609264 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.181-6603T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23609264 | |||||||
| chr13:23609320 | C | A | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.181-6547C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23609320 | |||||||
| chr13:23609346 | C | T | 2 | a0005c0008t0007g0029 a0005c0008t0007g0030 |
2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.181-6521C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23609346 | |||||||
| chr13:23609400 | G | A | 50 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(47): Show |
52 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.181-6467G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23609400 | |||||||
| chr13:23609582 | C | T | 1 | a0002c0002t0003g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.181-6285C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23609582 | |||||||
| chr13:23609696 | G | A | 2 | a0002c0002t0010g0020 a0004c0006t0001g0021 |
2 | HG02559.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.181-6171G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23609696 | |||||||
| chr13:23610050 | G | C | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-5817G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610050 | |||||||
| chr13:23610213 | A | G | 1 | a0001c0007t0028g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.181-5654A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610213 | |||||||
| chr13:23610382 | G | T | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.181-5485G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610382 | |||||||
| chr13:23610486 | ACCCCACT others(15): Show |
A | 1 | a0001c0001t0001g0322 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.181-5379_181-5358d others(24): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23610486 | ||||||
| chr13:23610489 | C | A | 1 | a0001c0004t0024g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.181-5378C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610489 | |||||||
| chr13:23610533 | T | TC | 102 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(99): Show |
105 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.181-5332dupC | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23610533 | ||||||
| chr13:23610543 | C | T | 1 | a0001c0007t0028g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.181-5324C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610543 | |||||||
| chr13:23610647 | C | T | 65 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(62): Show |
67 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.181-5220C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610647 | |||||||
| chr13:23610838 | A | G | 102 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(99): Show |
105 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.181-5029A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610838 | |||||||
| chr13:23610840 | GCATATAT others(5): Show |
G | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.181-5023_181-5012d others(14): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23610840 | ||||||
| chr13:23610871 | T | C | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-4996T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610871 | |||||||
| chr13:23610907 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.181-4960C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23610907 | |||||||
| chr13:23611097 | C | T | 1 | a0002c0002t0001g0101 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.181-4770C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611097 | |||||||
| chr13:23611111 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.181-4756C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611111 | |||||||
| chr13:23611121 | C | G | 1 | a0001c0001t0004g0295 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.181-4746C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611121 | |||||||
| chr13:23611121 | C | T | 1 | a0004c0006t0013g0371 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181-4746C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611121 | |||||||
| chr13:23611122 | A | G | 2 | a0001c0001t0020g0330 a0004c0006t0013g0371 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.181-4745A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611122 | |||||||
| chr13:23611125 | T | C | 2 | a0001c0001t0020g0330 a0004c0006t0013g0371 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.181-4742T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611125 | |||||||
| chr13:23611126 | G | A | 2 | a0001c0001t0020g0330 a0004c0006t0013g0371 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.181-4741G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611126 | |||||||
| chr13:23611126 | G | GCA | 112 | a0001c0001t0001g0084 a0001c0001t0001g0166 a0001c0001t0001g0167 others(109): Show |
117 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.181-4717_181-4716d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23611126 | ||||||
| chr13:23611126 | G | GCACA | 14 | a0001c0001t0001g0095 a0001c0001t0003g0196 a0001c0001t0010g0155 others(11): Show |
14 | HG00738.hp1 HG01257.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.181-4719_181-4716d others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23611126 | ||||||
| chr13:23611126 | GCACA | G | 49 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(46): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.181-4719_181-4716d others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23611126 | ||||||
| chr13:23611150 | ACT | A | 60 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0107 others(57): Show |
62 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.181-4715_181-4714d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23611150 | ||||||
| chr13:23611152 | T | A | 42 | a0002c0002t0001g0003 a0002c0002t0001g0024 a0002c0002t0001g0028 others(39): Show |
43 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.181-4715T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611152 | |||||||
| chr13:23611493 | G | A | 30 | a0002c0002t0001g0024 a0002c0002t0001g0028 a0002c0002t0006g0036 others(27): Show |
30 | HG00738.hp2 HG01074.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.181-4374G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611493 | |||||||
| chr13:23611779 | A | G | 1 | a0002c0005t0002g0100 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.181-4088A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611779 | |||||||
| chr13:23611817 | C | G | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-4050C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23611817 | |||||||
| chr13:23612068 | TTTGA | T | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-3796_181-3793d others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23612068 | ||||||
| chr13:23612203 | C | A | 1 | a0001c0004t0002g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.181-3664C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23612203 | |||||||
| chr13:23612504 | T | A | 1 | a0001c0001t0003g0278 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.181-3363T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23612504 | |||||||
| chr13:23612622 | A | G | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.181-3245A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23612622 | |||||||
| chr13:23612742 | G | A | 50 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0075 others(47): Show |
52 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.181-3125G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23612742 | |||||||
| chr13:23612790 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01433.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.181-3077C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23612790 | |||||||
| chr13:23612829 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.181-3038C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23612829 | |||||||
| chr13:23613043 | A | G | 1 | a0001c0007t0001g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.181-2824A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613043 | |||||||
| chr13:23613110 | T | C | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.181-2757T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613110 | |||||||
| chr13:23613162 | T | C | 22 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(19): Show |
22 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-2705T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613162 | |||||||
| chr13:23613277 | A | G | 1 | a0002c0005t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.181-2590A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613277 | |||||||
| chr13:23613346 | C | T | 3 | a0001c0001t0034g0154 a0003c0003t0006g0159 a0003c0003t0006g0160 |
3 | HG02258.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.181-2521C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613346 | |||||||
| chr13:23613364 | A | G | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.181-2503A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613364 | |||||||
| chr13:23613374 | C | T | 21 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(18): Show |
21 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.181-2493C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613374 | |||||||
| chr13:23613378 | T | A | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.181-2489T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613378 | |||||||
| chr13:23613433 | T | C | 1 | a0003c0003t0001g0197 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.181-2434T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613433 | |||||||
| chr13:23613450 | G | T | 21 | a0002c0002t0002g0312 a0002c0002t0005g0347 a0002c0002t0005g0348 others(18): Show |
21 | HG00621.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.181-2417G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613450 | |||||||
| chr13:23613593 | C | A | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.181-2274C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613593 | |||||||
| chr13:23613685 | T | G | 2 | a0001c0001t0020g0330 a0001c0007t0030g0331 |
2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.181-2182T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613685 | |||||||
| chr13:23613708 | C | T | 1 | a0003c0003t0001g0309 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.181-2159C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613708 | |||||||
| chr13:23613721 | C | T | 207 | a0001c0001t0001g0011 a0001c0001t0001g0054 a0001c0001t0001g0062 others(204): Show |
215 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.181-2146C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613721 | |||||||
| chr13:23613780 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.181-2087C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613780 | |||||||
| chr13:23613864 | C | T | 37 | a0001c0001t0001g0054 a0001c0001t0001g0158 a0001c0001t0003g0012 others(34): Show |
38 | HG00621.hp1 HG00642.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.181-2003C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613864 | |||||||
| chr13:23613900 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(204): Show |
216 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.181-1967T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613900 | |||||||
| chr13:23613918 | G | T | 3 | a0001c0001t0013g0343 a0001c0004t0024g0344 a0001c0004t0025g0345 |
3 | HG02451.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.181-1949G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613918 | |||||||
| chr13:23613929 | A | G | 2 | a0003c0003t0001g0291 a0003c0003t0001g0321 |
2 | NA18945.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.181-1938A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23613929 | |||||||
| chr13:23614021 | A | G | 1 | a0002c0002t0015g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.181-1846A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614021 | |||||||
| chr13:23614094 | G | T | 72 | a0001c0001t0001g0062 a0001c0001t0001g0158 a0001c0001t0001g0166 others(69): Show |
75 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.181-1773G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614094 | |||||||
| chr13:23614097 | TC | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 others(5): Show |
8 | HG01167.hp2 HG01175.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-1764delC | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614097 | ||||||
| chr13:23614131 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(144): Show |
153 | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(150): Show |
intron_variant | MODIFIER | c.181-1736T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614131 | |||||||
| chr13:23614168 | GACCTTCC | G | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.181-1695_181-1689d others(9): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614168 | ||||||
| chr13:23614220 | G | A | 1 | a0002c0002t0003g0005 | 2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.181-1647G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614220 | |||||||
| chr13:23614262 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0224 a0001c0001t0001g0225 others(24): Show |
28 | HG00735.hp1 HG01243.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.181-1605A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614262 | |||||||
| chr13:23614275 | A | C | 4 | a0002c0002t0015g0023 a0002c0002t0015g0031 a0002c0005t0012g0014 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-1592A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614275 | |||||||
| chr13:23614366 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.181-1501C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614366 | |||||||
| chr13:23614399 | T | C | 1 | a0002c0002t0023g0350 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.181-1468T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614399 | |||||||
| chr13:23614532 | CTG | C | 28 | a0001c0001t0001g0077 a0001c0001t0004g0004 a0001c0001t0004g0051 others(25): Show |
29 | HG00408.hp2 HG00423.hp1 HG02056.hp2 others(26): Show |
intron_variant | MODIFIER | c.181-1334_181-1333d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614532 | |||||||
| chr13:23614578 | A | G | 1 | a0009c0019t0001g0270 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.181-1289A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614578 | |||||||
| chr13:23614612 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.181-1255G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614612 | |||||||
| chr13:23614624 | C | G | 1 | a0001c0001t0020g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.181-1243C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614624 | |||||||
| chr13:23614648 | G | C | 47 | a0001c0001t0001g0049 a0001c0001t0001g0187 a0001c0001t0001g0282 others(44): Show |
49 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.181-1219G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614648 | |||||||
| chr13:23614675 | A | G | 1 | a0002c0002t0010g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.181-1192A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614675 | |||||||
| chr13:23614687 | G | A | 1 | a0001c0001t0002g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.181-1180G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614687 | |||||||
| chr13:23614746 | C | CACATATA others(7): Show |
4 | a0001c0001t0001g0241 a0001c0004t0017g0240 a0001c0004t0017g0242 others(1): Show |
4 | HG02056.hp1 NA18980.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-1120_181-1119i others(16): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CAT | 17 | a0001c0001t0004g0308 a0001c0001t0010g0155 a0001c0004t0002g0002 others(14): Show |
19 | HG00423.hp2 HG00621.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.181-1099_181-1098d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATAT | 8 | a0001c0001t0001g0095 a0002c0002t0001g0024 a0004c0006t0006g0025 others(5): Show |
8 | HG01884.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-1101_181-1098d others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATAT | 4 | a0001c0012t0001g0096 a0001c0012t0001g0097 a0002c0002t0010g0020 others(1): Show |
4 | HG02717.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-1103_181-1098d others(8): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(5): Show |
3 | a0002c0005t0012g0182 a0002c0005t0012g0183 a0006c0009t0007g0333 |
3 | HG02622.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.181-1109_181-1098d others(14): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(7): Show |
37 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0172 others(34): Show |
41 | HG00323.hp2 HG01109.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.181-1111_181-1098d others(16): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(9): Show |
18 | a0001c0001t0001g0011 a0001c0001t0001g0224 a0001c0001t0001g0225 others(15): Show |
19 | HG01069.hp1 HG01069.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.181-1113_181-1098d others(18): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(11): Show |
24 | a0001c0001t0001g0084 a0001c0001t0001g0219 a0001c0001t0001g0234 others(21): Show |
25 | HG00280.hp1 HG00639.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.181-1115_181-1098d others(20): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(13): Show |
10 | a0001c0001t0001g0054 a0001c0001t0001g0322 a0001c0001t0013g0343 others(7): Show |
10 | HG00621.hp1 HG02074.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.181-1117_181-1098d others(22): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(15): Show |
8 | a0001c0001t0001g0176 a0001c0001t0001g0317 a0001c0007t0001g0163 others(5): Show |
8 | HG01934.hp1 HG02145.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.181-1119_181-1098d others(24): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(17): Show |
4 | a0001c0001t0001g0281 a0002c0005t0005g0359 a0002c0005t0005g0369 others(1): Show |
4 | HG01978.hp1 HG02559.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-1098_181-1097i others(26): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(19): Show |
3 | a0001c0001t0001g0166 a0002c0002t0026g0105 a0004c0006t0009g0355 |
3 | HG01243.hp1 HG02273.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.181-1098_181-1097i others(28): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(21): Show |
1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.181-1098_181-1097i others(30): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | C | CATATATA others(29): Show |
1 | a0002c0005t0002g0046 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.181-1098_181-1097i others(38): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | CAT | C | 7 | a0001c0007t0030g0331 a0002c0002t0006g0036 a0002c0002t0010g0013 others(4): Show |
7 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-1099_181-1098d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | CATATATA others(1): Show |
C | 3 | a0001c0001t0001g0236 a0001c0001t0034g0154 a0004c0006t0001g0117 |
3 | HG03209.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.181-1105_181-1098d others(10): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614746 | CATATATA others(5): Show |
C | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.181-1109_181-1098d others(14): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 23614746 | ||||||
| chr13:23614769 | A | ATG | 3 | a0001c0001t0006g0108 a0001c0001t0006g0109 a0004c0006t0002g0113 |
3 | HG01109.hp1 HG01981.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.181-1098_181-1097i others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614769 | |||||||
| chr13:23614769 | A | G | 8 | a0001c0001t0001g0191 a0002c0002t0001g0003 a0002c0002t0001g0038 others(5): Show |
9 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.181-1098A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614769 | |||||||
| chr13:23614785 | T | TATACCTG others(3): Show |
10 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0001g0024 others(7): Show |
10 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.181-1082_181-1081i others(12): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614785 | |||||||
| chr13:23614884 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(176): Show |
187 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.181-983C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614884 | |||||||
| chr13:23614953 | G | A | 5 | a0001c0001t0001g0236 a0001c0001t0034g0154 a0002c0002t0026g0105 others(2): Show |
5 | HG01243.hp1 HG03209.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-914G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614953 | |||||||
| chr13:23614987 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(175): Show |
186 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.181-880G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23614987 | |||||||
| chr13:23615010 | T | C | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.181-857T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615010 | |||||||
| chr13:23615021 | A | T | 1 | a0003c0003t0001g0305 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.181-846A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615021 | |||||||
| chr13:23615055 | T | C | 11 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0001g0024 others(8): Show |
11 | HG01884.hp2 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.181-812T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615055 | |||||||
| chr13:23615056 | C | G | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.181-811C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615056 | |||||||
| chr13:23615205 | A | G | 2 | a0001c0001t0003g0196 a0002c0002t0003g0005 |
3 | HG00738.hp1 HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.181-662A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615205 | |||||||
| chr13:23615263 | G | A | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.181-604G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615263 | |||||||
| chr13:23615517 | C | T | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.181-350C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615517 | |||||||
| chr13:23615576 | A | G | 1 | a0004c0006t0013g0371 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181-291A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615576 | |||||||
| chr13:23615640 | A | G | 1 | a0005c0008t0007g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.181-227A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615640 | |||||||
| chr13:23615668 | T | C | 7 | a0001c0001t0001g0299 a0001c0001t0001g0301 a0001c0001t0004g0329 others(4): Show |
7 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-199T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615668 | |||||||
| chr13:23615780 | G | A | 2 | a0007c0011t0004g0121 a0007c0011t0004g0122 |
2 | HG00609.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.181-87G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615780 | |||||||
| chr13:23615784 | A | G | 7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-83A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 3/9 | chr13 | 23615784 | |||||||
| chr13:23616149 | C | T | 8 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.359+104C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616149 | |||||||
| chr13:23616343 | A | G | 2 | a0002c0005t0012g0182 a0002c0005t0012g0183 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.359+298A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616343 | |||||||
| chr13:23616349 | G | T | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.359+304G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616349 | |||||||
| chr13:23616390 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(124): Show |
134 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.359+345A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616390 | |||||||
| chr13:23616402 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(100): Show |
109 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.359+357T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616402 | |||||||
| chr13:23616576 | G | GTTTGT | 17 | a0001c0001t0033g0190 a0001c0007t0028g0189 a0002c0002t0001g0024 others(14): Show |
17 | HG01884.hp2 HG02559.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.359+543_359+547dup others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23616576 | ||||||
| chr13:23616580 | GT | G | 69 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(66): Show |
73 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.359+539delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23616580 | ||||||
| chr13:23616581 | T | TTTG | 100 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(97): Show |
105 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.359+538_359+539ins others(3): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23616581 | ||||||
| chr13:23616593 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(212): Show |
225 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.359+548C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616593 | |||||||
| chr13:23616644 | G | A | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.359+599G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616644 | |||||||
| chr13:23616680 | T | TC | 15 | a0001c0001t0002g0059 a0001c0001t0002g0257 a0002c0002t0002g0312 others(12): Show |
15 | HG01106.hp2 HG01433.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.359+636dupC | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23616680 | ||||||
| chr13:23616739 | C | T | 1 | a0002c0002t0015g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.359+694C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616739 | |||||||
| chr13:23616835 | T | A | 1 | a0004c0006t0032g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.359+790T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616835 | |||||||
| chr13:23616875 | G | A | 1 | a0001c0001t0003g0278 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.359+830G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616875 | |||||||
| chr13:23616879 | T | C | 4 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0013g0372 others(1): Show |
4 | HG02622.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+834T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616879 | |||||||
| chr13:23616897 | A | C | 4 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0013g0372 others(1): Show |
4 | HG02622.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+852A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616897 | |||||||
| chr13:23616948 | A | G | 1 | a0002c0002t0015g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.359+903A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23616948 | |||||||
| chr13:23617064 | G | A | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.359+1019G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617064 | |||||||
| chr13:23617092 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(166): Show |
178 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.359+1047G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617092 | |||||||
| chr13:23617172 | G | A | 2 | a0003c0003t0001g0263 a0003c0003t0001g0264 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.359+1127G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617172 | |||||||
| chr13:23617197 | C | T | 1 | a0003c0003t0001g0251 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.359+1152C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617197 | |||||||
| chr13:23617235 | G | T | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.359+1190G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617235 | |||||||
| chr13:23617253 | C | T | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.359+1208C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617253 | |||||||
| chr13:23617279 | G | T | 1 | a0002c0002t0002g0312 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.359+1234G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617279 | |||||||
| chr13:23617445 | A | AGTCT | 6 | a0001c0001t0033g0190 a0001c0007t0028g0189 a0002c0002t0001g0028 others(3): Show |
6 | HG02559.hp1 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.359+1402_359+1405d others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23617445 | ||||||
| chr13:23617498 | A | G | 1 | a0002c0010t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.359+1453A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617498 | |||||||
| chr13:23617637 | G | A | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.359+1592G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617637 | |||||||
| chr13:23617837 | G | C | 1 | a0001c0001t0004g0295 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.359+1792G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617837 | |||||||
| chr13:23617958 | G | A | 1 | a0003c0003t0001g0335 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.359+1913G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23617958 | |||||||
| chr13:23618070 | C | T | 1 | a0001c0004t0002g0218 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.359+2025C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618070 | |||||||
| chr13:23618215 | A | G | 2 | a0001c0001t0001g0077 a0002c0002t0001g0134 |
2 | HG02071.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.359+2170A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618215 | |||||||
| chr13:23618369 | T | C | 3 | a0002c0002t0001g0147 a0002c0002t0001g0148 a0002c0002t0002g0146 |
3 | NA18980.hp2 NA18994.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.359+2324T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618369 | |||||||
| chr13:23618654 | A | G | 1 | a0001c0004t0002g0092 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.359+2609A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618654 | |||||||
| chr13:23618768 | G | C | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0006c0009t0007g0333 |
3 | HG02622.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.359+2723G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618768 | |||||||
| chr13:23618808 | C | T | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.359+2763C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618808 | |||||||
| chr13:23618814 | T | C | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.359+2769T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618814 | |||||||
| chr13:23618835 | C | T | 9 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.359+2790C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618835 | |||||||
| chr13:23618839 | G | A | 1 | a0002c0002t0001g0129 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.359+2794G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618839 | |||||||
| chr13:23618842 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.359+2797A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618842 | |||||||
| chr13:23618911 | C | T | 1 | a0001c0001t0003g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.359+2866C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618911 | |||||||
| chr13:23618998 | C | T | 2 | a0001c0001t0004g0078 a0001c0001t0004g0308 |
2 | HG02083.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.359+2953C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23618998 | |||||||
| chr13:23619034 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.359+2989C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23619034 | |||||||
| chr13:23619101 | G | A | 1 | a0002c0005t0002g0138 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.359+3056G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23619101 | |||||||
| chr13:23619220 | C | CAT | 203 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(200): Show |
213 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.359+3176_359+3177d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23619220 | ||||||
| chr13:23619365 | C | T | 1 | a0001c0001t0004g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.359+3320C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23619365 | |||||||
| chr13:23619482 | TATGGAA | T | 3 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 |
3 | HG01109.hp1 HG01981.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.359+3439_359+3444d others(8): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23619482 | ||||||
| chr13:23619603 | T | C | 1 | a0003c0003t0001g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.359+3558T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23619603 | |||||||
| chr13:23619904 | C | G | 4 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0013g0372 others(1): Show |
4 | HG02622.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+3859C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23619904 | |||||||
| chr13:23619981 | T | C | 15 | a0001c0001t0002g0059 a0001c0001t0002g0257 a0002c0002t0002g0312 others(12): Show |
15 | HG01106.hp2 HG01433.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.359+3936T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23619981 | |||||||
| chr13:23620112 | G | A | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.359+4067G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23620112 | |||||||
| chr13:23620172 | T | G | 1 | a0001c0004t0002g0215 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.359+4127T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23620172 | |||||||
| chr13:23620242 | A | C | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.359+4197A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23620242 | |||||||
| chr13:23620278 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(185): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.359+4233A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23620278 | |||||||
| chr13:23620385 | C | G | 1 | a0002c0005t0002g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.359+4340C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23620385 | |||||||
| chr13:23620493 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.359+4448C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23620493 | |||||||
| chr13:23620543 | C | T | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.359+4498C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23620543 | |||||||
| chr13:23620770 | G | A | 1 | a0004c0006t0013g0371 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.359+4725G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23620770 | |||||||
| chr13:23621133 | G | A | 1 | a0001c0001t0003g0337 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.359+5088G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23621133 | |||||||
| chr13:23621151 | C | T | 1 | a0001c0004t0002g0279 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.359+5106C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23621151 | |||||||
| chr13:23621311 | C | T | 2 | a0002c0002t0001g0128 a0002c0002t0001g0149 |
2 | HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.359+5266C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23621311 | |||||||
| chr13:23621419 | G | A | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.360-5288G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23621419 | |||||||
| chr13:23621538 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(183): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.360-5169G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23621538 | |||||||
| chr13:23621702 | G | T | 1 | a0003c0003t0006g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.360-5005G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23621702 | |||||||
| chr13:23621778 | TAA | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(191): Show |
204 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.360-4916_360-4915d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23621778 | ||||||
| chr13:23621906 | G | A | 1 | a0001c0001t0020g0330 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.360-4801G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23621906 | |||||||
| chr13:23622009 | G | C | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.360-4698G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622009 | |||||||
| chr13:23622011 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG01433.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.360-4696G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622011 | |||||||
| chr13:23622039 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(101): Show |
109 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.360-4668G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622039 | |||||||
| chr13:23622169 | C | T | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(7): Show |
11 | HG00280.hp1 HG01070.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.360-4538C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622169 | |||||||
| chr13:23622264 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(198): Show |
211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.360-4443T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622264 | |||||||
| chr13:23622273 | TA | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(183): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.360-4431delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23622273 | ||||||
| chr13:23622324 | G | A | 1 | a0002c0005t0002g0136 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.360-4383G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622324 | |||||||
| chr13:23622428 | T | A | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.360-4279T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622428 | |||||||
| chr13:23622442 | TA | T | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0013g0372 |
3 | HG02647.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.360-4259delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23622442 | ||||||
| chr13:23622605 | A | T | 1 | a0002c0002t0001g0123 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.360-4102A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622605 | |||||||
| chr13:23622614 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.360-4093A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622614 | |||||||
| chr13:23622694 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.360-4013A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622694 | |||||||
| chr13:23622712 | G | A | 1 | a0002c0005t0012g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.360-3995G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622712 | |||||||
| chr13:23622928 | T | A | 1 | a0001c0022t0016g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.360-3779T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23622928 | |||||||
| chr13:23623042 | T | C | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.360-3665T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623042 | |||||||
| chr13:23623095 | C | T | 5 | a0001c0001t0001g0236 a0001c0001t0034g0154 a0002c0002t0026g0105 others(2): Show |
5 | HG01243.hp1 HG03209.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.360-3612C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623095 | |||||||
| chr13:23623141 | C | T | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.360-3566C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623141 | |||||||
| chr13:23623338 | A | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.360-3369A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623338 | |||||||
| chr13:23623540 | G | A | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.360-3167G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623540 | |||||||
| chr13:23623561 | C | T | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.360-3146C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623561 | |||||||
| chr13:23623602 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.360-3105C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623602 | |||||||
| chr13:23623650 | G | A | 1 | a0001c0001t0006g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.360-3057G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623650 | |||||||
| chr13:23623654 | T | C | 10 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 others(7): Show |
11 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.360-3053T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623654 | |||||||
| chr13:23623673 | A | G | 1 | a0003c0003t0001g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.360-3034A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623673 | |||||||
| chr13:23623726 | A | T | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0002c0002t0001g0042 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.360-2981A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623726 | |||||||
| chr13:23623963 | C | A | 1 | a0001c0001t0041g0076 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.360-2744C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623963 | |||||||
| chr13:23623988 | C | G | 10 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 others(7): Show |
11 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.360-2719C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23623988 | |||||||
| chr13:23624132 | A | C | 5 | a0001c0001t0043g0178 a0001c0004t0042g0181 a0003c0003t0018g0162 others(2): Show |
5 | HG02559.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.360-2575A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624132 | |||||||
| chr13:23624265 | A | G | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.360-2442A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624265 | |||||||
| chr13:23624321 | C | T | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.360-2386C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624321 | |||||||
| chr13:23624352 | C | T | 1 | a0003c0003t0006g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.360-2355C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624352 | |||||||
| chr13:23624568 | T | C | 1 | a0003c0003t0022g0008 | 2 | NA18950.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.360-2139T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624568 | |||||||
| chr13:23624619 | G | A | 10 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 others(7): Show |
11 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.360-2088G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624619 | |||||||
| chr13:23624689 | C | T | 1 | a0004c0006t0001g0132 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.360-2018C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624689 | |||||||
| chr13:23624704 | G | C | 20 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(17): Show |
21 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.360-2003G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624704 | |||||||
| chr13:23624709 | T | C | 4 | a0001c0001t0033g0190 a0001c0007t0028g0189 a0002c0002t0001g0028 others(1): Show |
4 | HG02559.hp1 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.360-1998T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624709 | |||||||
| chr13:23624793 | C | T | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.360-1914C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624793 | |||||||
| chr13:23624812 | G | A | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0013g0372 |
3 | HG02647.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.360-1895G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624812 | |||||||
| chr13:23624827 | T | C | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.360-1880T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23624827 | |||||||
| chr13:23625057 | C | T | 1 | a0003c0003t0001g0321 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.360-1650C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625057 | |||||||
| chr13:23625058 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(213): Show |
226 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.360-1649G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625058 | |||||||
| chr13:23625326 | C | CT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(192): Show |
204 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.360-1361dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23625326 | ||||||
| chr13:23625326 | C | CTT | 14 | a0001c0001t0001g0054 a0001c0001t0001g0225 a0001c0001t0001g0226 others(11): Show |
15 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.360-1362_360-1361d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23625326 | ||||||
| chr13:23625474 | G | A | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.360-1233G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625474 | |||||||
| chr13:23625477 | C | T | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.360-1230C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625477 | |||||||
| chr13:23625485 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(120): Show |
129 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.360-1222C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625485 | |||||||
| chr13:23625605 | G | A | 1 | a0002c0017t0011g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.360-1102G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625605 | |||||||
| chr13:23625620 | G | A | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360-1087G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625620 | |||||||
| chr13:23625657 | T | C | 1 | a0001c0004t0002g0060 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.360-1050T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625657 | |||||||
| chr13:23625754 | C | T | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.360-953C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625754 | |||||||
| chr13:23625930 | T | A | 7 | a0003c0003t0001g0291 a0003c0003t0001g0302 a0003c0003t0001g0306 others(4): Show |
8 | NA18945.hp2 NA18951.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.360-777T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625930 | |||||||
| chr13:23625931 | T | G | 1 | a0002c0002t0003g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.360-776T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23625931 | |||||||
| chr13:23626037 | T | G | 2 | a0006c0009t0007g0007 a0006c0009t0007g0333 |
3 | HG00280.hp1 HG01070.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.360-670T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626037 | |||||||
| chr13:23626101 | T | G | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.360-606T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626101 | |||||||
| chr13:23626115 | C | T | 10 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 others(7): Show |
11 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.360-592C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626115 | |||||||
| chr13:23626127 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(211): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.360-580G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626127 | |||||||
| chr13:23626185 | A | ATGTGTGT others(7): Show |
1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360-521_360-520ins others(14): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626185 | ||||||
| chr13:23626187 | C | CTG | 8 | a0001c0001t0001g0172 a0001c0001t0003g0296 a0001c0001t0004g0063 others(5): Show |
8 | HG01993.hp1 HG02135.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.360-485_360-484dup others(2): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | C | CTGTG | 29 | a0001c0001t0001g0077 a0001c0001t0001g0095 a0001c0001t0004g0004 others(26): Show |
30 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.360-487_360-484dup others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | C | CTGTGTG | 71 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(68): Show |
75 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.360-489_360-484dup others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | C | CTGTGTGT others(1): Show |
25 | a0001c0001t0001g0054 a0001c0001t0001g0236 a0001c0001t0001g0316 others(22): Show |
26 | HG00621.hp1 HG01261.hp2 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.360-491_360-484dup others(8): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | C | CTGTGTGT others(3): Show |
15 | a0001c0001t0001g0271 a0001c0001t0020g0330 a0001c0004t0002g0173 others(12): Show |
15 | HG01243.hp1 HG02129.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.360-493_360-484dup others(10): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0294 a0004c0006t0013g0371 |
2 | NA19043.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.360-495_360-484dup others(12): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | C | CTGTGTGT others(7): Show |
7 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0027g0223 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.360-497_360-484dup others(14): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | C | CTGTGTGT others(9): Show |
2 | a0001c0001t0020g0332 a0002c0005t0012g0182 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.360-499_360-484dup others(16): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | C | G | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.360-520C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626187 | |||||||
| chr13:23626187 | CTG | C | 9 | a0001c0001t0001g0201 a0001c0001t0019g0292 a0001c0001t0033g0190 others(6): Show |
10 | HG01496.hp1 HG02723.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.360-485_360-484del others(2): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | CTGTG | C | 153 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0062 others(150): Show |
157 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.360-487_360-484del others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626187 | CTGTGTG | C | 10 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 others(7): Show |
11 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.360-489_360-484del others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 23626187 | ||||||
| chr13:23626227 | G | T | 1 | a0008c0014t0003g0156 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.360-480G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626227 | |||||||
| chr13:23626243 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0237 a0001c0004t0002g0060 |
3 | NA18973.hp2 NA18977.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.360-464A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626243 | |||||||
| chr13:23626325 | T | G | 5 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0003g0311 others(2): Show |
5 | HG01261.hp2 HG01975.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.360-382T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626325 | |||||||
| chr13:23626338 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.360-369G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626338 | |||||||
| chr13:23626393 | T | G | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.360-314T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626393 | |||||||
| chr13:23626448 | A | G | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.360-259A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626448 | |||||||
| chr13:23626633 | T | G | 1 | a0006c0009t0007g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.360-74T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626633 | |||||||
| chr13:23626655 | C | G | 22 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(19): Show |
23 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.360-52C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626655 | |||||||
| chr13:23626672 | A | G | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.360-35A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 4/9 | chr13 | 23626672 | |||||||
| chr13:23627127 | G | A | 9 | a0001c0001t0001g0166 a0001c0001t0013g0343 a0001c0004t0024g0344 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+335G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23627127 | |||||||
| chr13:23627265 | T | C | 8 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(5): Show |
9 | HG00280.hp1 HG01070.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.445+473T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23627265 | |||||||
| chr13:23627428 | A | T | 2 | a0002c0005t0012g0182 a0002c0005t0012g0183 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.445+636A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23627428 | |||||||
| chr13:23627463 | T | C | 1 | a0002c0002t0003g0133 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.445+671T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23627463 | |||||||
| chr13:23627532 | C | T | 4 | a0001c0001t0033g0190 a0001c0007t0028g0189 a0002c0002t0001g0028 others(1): Show |
4 | HG02559.hp1 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+740C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23627532 | |||||||
| chr13:23627744 | G | A | 10 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 others(7): Show |
11 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+952G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23627744 | |||||||
| chr13:23627938 | C | A | 7 | a0002c0002t0001g0003 a0002c0002t0001g0038 a0002c0002t0001g0040 others(4): Show |
8 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+1146C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23627938 | |||||||
| chr13:23628012 | CAA | C | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(7): Show |
11 | HG00280.hp1 HG01070.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+1222_445+1223d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23628012 | ||||||
| chr13:23628016 | T | G | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0002g0173 others(7): Show |
11 | HG00280.hp1 HG01070.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+1224T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628016 | |||||||
| chr13:23628108 | G | T | 25 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(22): Show |
26 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.445+1316G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628108 | |||||||
| chr13:23628148 | G | C | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.445+1356G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628148 | |||||||
| chr13:23628211 | G | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(183): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.445+1419G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628211 | |||||||
| chr13:23628266 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(158): Show |
169 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.445+1474A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628266 | |||||||
| chr13:23628332 | T | C | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.445+1540T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628332 | |||||||
| chr13:23628509 | C | T | 1 | a0002c0002t0009g0360 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.445+1717C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628509 | |||||||
| chr13:23628519 | G | C | 2 | a0002c0005t0002g0085 a0002c0005t0002g0086 |
2 | HG00323.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.445+1727G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628519 | |||||||
| chr13:23628767 | G | GTA | 6 | a0001c0001t0008g0010 a0001c0001t0008g0261 a0001c0001t0008g0262 others(3): Show |
7 | NA18957.hp2 NA18978.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+1988_445+1989d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23628767 | ||||||
| chr13:23628849 | A | C | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.445+2057A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628849 | |||||||
| chr13:23628888 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(98): Show |
106 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.445+2096C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23628888 | |||||||
| chr13:23629086 | C | CT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(119): Show |
128 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.445+2308dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23629086 | ||||||
| chr13:23629134 | G | T | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.445+2342G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23629134 | |||||||
| chr13:23629213 | G | A | 6 | a0001c0001t0001g0236 a0001c0001t0027g0223 a0001c0001t0034g0154 others(3): Show |
6 | HG01243.hp1 HG01361.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+2421G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23629213 | |||||||
| chr13:23629233 | G | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(98): Show |
106 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.445+2441G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23629233 | |||||||
| chr13:23629315 | G | T | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.445+2523G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23629315 | |||||||
| chr13:23629386 | C | T | 8 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0003g0231 others(5): Show |
8 | HG00280.hp2 HG00642.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.445+2594C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23629386 | |||||||
| chr13:23629387 | G | A | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.445+2595G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23629387 | |||||||
| chr13:23629443 | A | G | 1 | a0001c0001t0004g0295 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.445+2651A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23629443 | |||||||
| chr13:23629499 | A | G | 2 | a0001c0001t0027g0223 a0002c0002t0026g0105 |
2 | HG01243.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.445+2707A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23629499 | |||||||
| chr13:23630202 | C | T | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.445+3410C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23630202 | |||||||
| chr13:23630302 | T | TA | 52 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0224 others(49): Show |
54 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.445+3532dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23630302 | ||||||
| chr13:23630302 | T | TAA | 30 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0093 others(27): Show |
32 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.445+3531_445+3532d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23630302 | ||||||
| chr13:23630302 | T | TAAA | 28 | a0001c0001t0001g0077 a0001c0001t0003g0339 a0001c0001t0003g0340 others(25): Show |
29 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.445+3530_445+3532d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23630302 | ||||||
| chr13:23630302 | TA | T | 26 | a0001c0001t0001g0187 a0001c0001t0001g0200 a0001c0001t0001g0288 others(23): Show |
26 | HG00438.hp1 HG01496.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.445+3532delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23630302 | ||||||
| chr13:23630403 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.445+3611C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23630403 | |||||||
| chr13:23630439 | C | A | 1 | a0001c0001t0043g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.445+3647C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23630439 | |||||||
| chr13:23630460 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.445+3668C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23630460 | |||||||
| chr13:23630523 | A | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.445+3731A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23630523 | |||||||
| chr13:23630752 | C | G | 19 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.445+3960C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23630752 | |||||||
| chr13:23630816 | C | T | 3 | a0001c0001t0004g0308 a0003c0003t0001g0235 a0003c0003t0001g0307 |
3 | HG02083.hp2 NA18946.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.445+4024C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23630816 | |||||||
| chr13:23631056 | A | G | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.445+4264A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631056 | |||||||
| chr13:23631273 | T | C | 10 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 others(7): Show |
11 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+4481T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631273 | |||||||
| chr13:23631364 | C | T | 1 | a0002c0002t0002g0146 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.445+4572C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631364 | |||||||
| chr13:23631399 | C | T | 1 | a0003c0003t0001g0243 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.445+4607C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631399 | |||||||
| chr13:23631400 | G | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.445+4608G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631400 | |||||||
| chr13:23631433 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.445+4641G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631433 | |||||||
| chr13:23631494 | G | A | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.445+4702G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631494 | |||||||
| chr13:23631518 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.445+4726C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631518 | |||||||
| chr13:23631602 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.445+4810T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631602 | |||||||
| chr13:23631626 | T | C | 1 | a0001c0001t0004g0064 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.445+4834T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631626 | |||||||
| chr13:23631905 | G | A | 1 | a0001c0001t0040g0090 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.445+5113G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631905 | |||||||
| chr13:23631952 | T | C | 1 | a0002c0002t0013g0372 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.445+5160T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23631952 | |||||||
| chr13:23632040 | T | A | 2 | a0001c0013t0003g0259 a0001c0013t0003g0260 |
2 | HG00280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.445+5248T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632040 | |||||||
| chr13:23632280 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.445+5488G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632280 | |||||||
| chr13:23632325 | T | C | 79 | a0001c0001t0001g0077 a0001c0001t0001g0095 a0001c0001t0001g0158 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.445+5533T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632325 | |||||||
| chr13:23632341 | A | C | 1 | a0002c0002t0003g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.445+5549A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632341 | |||||||
| chr13:23632488 | C | G | 1 | a0001c0001t0004g0068 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.445+5696C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632488 | |||||||
| chr13:23632489 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(158): Show |
169 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.445+5697A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632489 | |||||||
| chr13:23632592 | T | C | 1 | a0002c0002t0013g0372 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.445+5800T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632592 | |||||||
| chr13:23632745 | C | A | 19 | a0001c0001t0001g0095 a0001c0001t0001g0224 a0001c0001t0001g0225 others(16): Show |
20 | HG00280.hp1 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.445+5953C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632745 | |||||||
| chr13:23632894 | C | T | 2 | a0001c0001t0033g0190 a0002c0002t0001g0028 |
2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.445+6102C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23632894 | |||||||
| chr13:23633002 | C | A | 3 | a0001c0001t0033g0190 a0002c0002t0001g0028 a0004c0006t0001g0021 |
3 | HG02559.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.445+6210C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633002 | |||||||
| chr13:23633004 | C | G | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.445+6212C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633004 | |||||||
| chr13:23633044 | C | T | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.445+6252C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633044 | |||||||
| chr13:23633085 | G | T | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.445+6293G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633085 | |||||||
| chr13:23633111 | C | CT | 74 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0001g0191 others(71): Show |
78 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.445+6336dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23633111 | ||||||
| chr13:23633111 | C | CTT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(107): Show |
115 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(112): Show |
intron_variant | MODIFIER | c.445+6335_445+6336d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23633111 | ||||||
| chr13:23633111 | C | CTTT | 11 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0317 others(8): Show |
12 | HG00280.hp1 HG01070.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.445+6334_445+6336d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23633111 | ||||||
| chr13:23633111 | CT | C | 6 | a0001c0001t0001g0327 a0001c0001t0010g0155 a0001c0001t0033g0190 others(3): Show |
6 | HG03225.hp1 HG03471.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+6336delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23633111 | ||||||
| chr13:23633308 | G | C | 31 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0091 others(28): Show |
33 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.445+6516G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633308 | |||||||
| chr13:23633377 | C | G | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0013g0372 |
3 | HG02647.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.445+6585C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633377 | |||||||
| chr13:23633529 | ACTC | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(98): Show |
106 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.445+6741_445+6743d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23633529 | ||||||
| chr13:23633612 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(125): Show |
134 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.445+6820G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633612 | |||||||
| chr13:23633710 | G | A | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0013g0372 |
3 | HG02647.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.445+6918G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633710 | |||||||
| chr13:23633801 | A | G | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.445+7009A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633801 | |||||||
| chr13:23633809 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(182): Show |
194 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.445+7017G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633809 | |||||||
| chr13:23633813 | C | T | 3 | a0002c0005t0002g0085 a0002c0005t0002g0086 a0002c0005t0002g0087 |
3 | HG00323.hp2 HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.445+7021C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633813 | |||||||
| chr13:23633837 | G | A | 7 | a0001c0001t0003g0012 a0001c0001t0003g0337 a0001c0001t0003g0338 others(4): Show |
8 | NA18941.hp1 NA18946.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.445+7045G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633837 | |||||||
| chr13:23633884 | A | C | 3 | a0001c0001t0001g0095 a0001c0012t0001g0096 a0001c0012t0001g0097 |
3 | HG02717.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.445+7092A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633884 | |||||||
| chr13:23633898 | T | C | 1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.445+7106T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633898 | |||||||
| chr13:23633942 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.445+7150C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633942 | |||||||
| chr13:23633976 | G | T | 1 | a0004c0006t0013g0371 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+7184G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23633976 | |||||||
| chr13:23634127 | A | T | 3 | a0002c0005t0014g0141 a0002c0005t0014g0142 a0002c0005t0014g0145 |
3 | HG02896.hp2 HG02897.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.445+7335A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23634127 | |||||||
| chr13:23634165 | T | C | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445+7373T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23634165 | |||||||
| chr13:23634259 | G | A | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445+7467G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23634259 | |||||||
| chr13:23634451 | G | A | 2 | a0005c0008t0007g0019 a0005c0008t0007g0022 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.445+7659G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23634451 | |||||||
| chr13:23634601 | C | A | 1 | a0002c0002t0001g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.445+7809C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23634601 | |||||||
| chr13:23634690 | A | G | 25 | a0001c0001t0001g0191 a0001c0001t0006g0108 a0001c0001t0006g0109 others(22): Show |
26 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.445+7898A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23634690 | |||||||
| chr13:23634788 | T | C | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.445+7996T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23634788 | |||||||
| chr13:23634951 | T | C | 1 | a0002c0005t0002g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.445+8159T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23634951 | |||||||
| chr13:23635097 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(219): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.445+8305T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635097 | |||||||
| chr13:23635163 | A | T | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.445+8371A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635163 | |||||||
| chr13:23635167 | C | T | 6 | a0002c0002t0015g0026 a0004c0006t0006g0025 a0004c0006t0006g0027 others(3): Show |
6 | HG01884.hp2 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.445+8375C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635167 | |||||||
| chr13:23635247 | T | C | 1 | a0002c0002t0003g0144 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.445+8455T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635247 | |||||||
| chr13:23635482 | G | A | 29 | a0001c0001t0001g0077 a0001c0001t0004g0004 a0001c0001t0004g0051 others(26): Show |
30 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.445+8690G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635482 | |||||||
| chr13:23635642 | G | A | 60 | a0001c0001t0001g0077 a0001c0001t0001g0158 a0001c0001t0003g0012 others(57): Show |
63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.445+8850G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635642 | |||||||
| chr13:23635649 | G | C | 1 | a0002c0002t0001g0040 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.445+8857G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635649 | |||||||
| chr13:23635656 | G | A | 1 | a0003c0003t0001g0305 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.445+8864G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635656 | |||||||
| chr13:23635690 | T | C | 5 | a0001c0001t0001g0236 a0001c0001t0034g0154 a0002c0002t0026g0105 others(2): Show |
5 | HG01243.hp1 HG03209.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+8898T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635690 | |||||||
| chr13:23635875 | T | C | 5 | a0001c0001t0001g0236 a0001c0001t0034g0154 a0002c0002t0026g0105 others(2): Show |
5 | HG01243.hp1 HG03209.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+9083T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635875 | |||||||
| chr13:23635885 | A | G | 6 | a0002c0002t0006g0036 a0002c0002t0010g0013 a0002c0002t0010g0020 others(3): Show |
6 | HG02630.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+9093A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635885 | |||||||
| chr13:23635960 | C | G | 11 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0025g0345 others(8): Show |
12 | HG00280.hp1 HG01070.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.445+9168C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23635960 | |||||||
| chr13:23636075 | A | G | 1 | a0004c0006t0001g0021 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.445+9283A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636075 | |||||||
| chr13:23636139 | C | T | 2 | a0003c0003t0006g0159 a0003c0003t0006g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.445+9347C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636139 | |||||||
| chr13:23636165 | G | T | 2 | a0006c0009t0007g0007 a0006c0009t0007g0333 |
3 | HG00280.hp1 HG01070.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.445+9373G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636165 | |||||||
| chr13:23636314 | A | G | 4 | a0001c0001t0033g0190 a0001c0007t0028g0189 a0002c0002t0001g0028 others(1): Show |
4 | HG02559.hp1 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+9522A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636314 | |||||||
| chr13:23636436 | G | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(179): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.445+9644G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636436 | |||||||
| chr13:23636576 | C | T | 1 | a0004c0006t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.445+9784C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636576 | |||||||
| chr13:23636634 | G | A | 116 | a0001c0001t0001g0049 a0001c0001t0001g0062 a0001c0001t0001g0075 others(113): Show |
119 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.445+9842G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636634 | |||||||
| chr13:23636672 | A | G | 117 | a0001c0001t0001g0049 a0001c0001t0001g0062 a0001c0001t0001g0075 others(114): Show |
120 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.445+9880A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636672 | |||||||
| chr13:23636807 | G | A | 1 | a0001c0004t0036g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.445+10015G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636807 | |||||||
| chr13:23636857 | C | T | 1 | a0001c0007t0011g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.445+10065C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636857 | |||||||
| chr13:23636888 | G | C | 1 | a0002c0002t0013g0372 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.445+10096G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23636888 | |||||||
| chr13:23637040 | AGTT | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0045 others(62): Show |
71 | HG00323.hp1 HG00639.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.445+10255_445+1025 others(7): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23637040 | ||||||
| chr13:23637074 | A | G | 11 | a0001c0001t0001g0191 a0001c0001t0001g0236 a0001c0004t0025g0345 others(8): Show |
11 | HG00738.hp2 HG01074.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.445+10282A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637074 | |||||||
| chr13:23637227 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0062 others(118): Show |
127 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.445+10435T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637227 | |||||||
| chr13:23637296 | G | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0062 others(203): Show |
215 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.445+10504G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637296 | |||||||
| chr13:23637376 | C | T | 4 | a0001c0001t0033g0190 a0001c0007t0028g0189 a0002c0002t0001g0028 others(1): Show |
4 | HG03225.hp1 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+10584C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637376 | |||||||
| chr13:23637411 | A | C | 2 | a0001c0001t0027g0223 a0001c0007t0001g0163 |
2 | HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.445+10619A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637411 | |||||||
| chr13:23637418 | G | A | 1 | a0004c0006t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.445+10626G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637418 | |||||||
| chr13:23637429 | GCTGAGTC others(9): Show |
G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0314 |
3 | HG01069.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.445+10640_445+1065 others(20): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23637429 | ||||||
| chr13:23637552 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0010g0155 a0001c0001t0034g0154 others(1): Show |
4 | HG02723.hp2 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.445+10760C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637552 | |||||||
| chr13:23637553 | G | A | 34 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(31): Show |
36 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.445+10761G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637553 | |||||||
| chr13:23637659 | A | AT | 5 | a0002c0002t0001g0003 a0002c0002t0001g0038 a0002c0002t0001g0040 others(2): Show |
6 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+10874dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23637659 | ||||||
| chr13:23637836 | C | T | 1 | a0001c0001t0010g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.445+11044C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637836 | |||||||
| chr13:23637837 | G | A | 1 | a0002c0002t0016g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.445+11045G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637837 | |||||||
| chr13:23637901 | C | T | 1 | a0003c0003t0001g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.445+11109C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637901 | |||||||
| chr13:23637946 | C | T | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.445+11154C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637946 | |||||||
| chr13:23637969 | G | A | 1 | a0003c0003t0001g0083 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.445+11177G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23637969 | |||||||
| chr13:23638114 | G | T | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.445+11322G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638114 | |||||||
| chr13:23638115 | A | T | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.445+11323A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638115 | |||||||
| chr13:23638159 | A | AGACGTTA others(35): Show |
76 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(73): Show |
80 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.445+11369_445+1141 others(46): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23638159 | ||||||
| chr13:23638173 | C | CGTAGACT others(24): Show |
2 | a0001c0001t0010g0155 a0004c0006t0013g0371 |
2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.445+11406_445+1140 others(35): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23638173 | ||||||
| chr13:23638214 | G | A | 78 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445+11422G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638214 | |||||||
| chr13:23638252 | G | C | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445+11460G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638252 | |||||||
| chr13:23638273 | A | G | 28 | a0001c0001t0004g0004 a0001c0001t0004g0051 a0001c0001t0004g0055 others(25): Show |
29 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.445+11481A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638273 | |||||||
| chr13:23638347 | G | A | 82 | a0001c0001t0001g0095 a0001c0001t0001g0158 a0001c0001t0003g0012 others(79): Show |
86 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.445+11555G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638347 | |||||||
| chr13:23638594 | G | C | 5 | a0001c0001t0001g0241 a0002c0002t0005g0353 a0002c0002t0005g0358 others(2): Show |
5 | NA18979.hp1 NA18980.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+11802G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638594 | |||||||
| chr13:23638680 | C | T | 3 | a0002c0002t0015g0023 a0002c0002t0015g0026 a0002c0002t0015g0031 |
3 | HG02257.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.445+11888C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638680 | |||||||
| chr13:23638743 | A | G | 7 | a0002c0002t0006g0036 a0002c0002t0010g0013 a0002c0002t0010g0018 others(4): Show |
7 | HG02630.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.445+11951A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638743 | |||||||
| chr13:23638812 | C | T | 3 | a0001c0022t0016g0326 a0002c0002t0013g0372 a0002c0002t0026g0105 |
3 | HG01243.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.445+12020C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638812 | |||||||
| chr13:23638815 | T | C | 65 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(62): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.445+12023T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638815 | |||||||
| chr13:23638839 | C | T | 1 | a0002c0005t0039g0125 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.445+12047C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638839 | |||||||
| chr13:23638936 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.445+12144G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638936 | |||||||
| chr13:23638940 | G | A | 1 | a0003c0003t0001g0265 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.445+12148G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638940 | |||||||
| chr13:23638981 | T | C | 78 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445+12189T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23638981 | |||||||
| chr13:23639021 | A | G | 3 | a0001c0004t0017g0205 a0001c0004t0017g0240 a0001c0004t0017g0242 |
3 | HG02056.hp1 NA18939.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.445+12229A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639021 | |||||||
| chr13:23639040 | T | C | 1 | a0002c0010t0001g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.445+12248T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639040 | |||||||
| chr13:23639074 | T | C | 8 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0200 others(5): Show |
8 | HG00735.hp2 HG01099.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.445+12282T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639074 | |||||||
| chr13:23639125 | G | T | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.445+12333G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639125 | |||||||
| chr13:23639247 | G | T | 7 | a0005c0008t0007g0019 a0005c0008t0007g0022 a0005c0008t0007g0029 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.445+12455G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639247 | |||||||
| chr13:23639248 | C | T | 7 | a0005c0008t0007g0019 a0005c0008t0007g0022 a0005c0008t0007g0029 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.445+12456C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639248 | |||||||
| chr13:23639309 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(288): Show |
304 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.445+12517T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639309 | |||||||
| chr13:23639404 | T | A | 6 | a0001c0007t0030g0331 a0001c0022t0016g0326 a0002c0002t0015g0023 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+12612T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639404 | |||||||
| chr13:23639437 | C | T | 5 | a0001c0001t0010g0155 a0001c0001t0020g0330 a0001c0001t0020g0332 others(2): Show |
5 | HG02647.hp1 HG03471.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+12645C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639437 | |||||||
| chr13:23639684 | A | T | 1 | a0001c0001t0001g0317 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.445+12892A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639684 | |||||||
| chr13:23639754 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.445+12962G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639754 | |||||||
| chr13:23639780 | G | A | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445+12988G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639780 | |||||||
| chr13:23639820 | C | G | 7 | a0005c0008t0007g0019 a0005c0008t0007g0022 a0005c0008t0007g0029 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.445+13028C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639820 | |||||||
| chr13:23639893 | A | C | 2 | a0001c0022t0016g0326 a0002c0002t0026g0105 |
2 | HG01243.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.445+13101A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639893 | |||||||
| chr13:23639957 | C | T | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445+13165C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23639957 | |||||||
| chr13:23640348 | A | G | 1 | a0001c0004t0002g0210 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.445+13556A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640348 | |||||||
| chr13:23640398 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0035g0298 |
2 | NA19043.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.445+13606G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640398 | |||||||
| chr13:23640428 | A | G | 1 | a0001c0001t0004g0151 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.445+13636A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640428 | |||||||
| chr13:23640433 | T | C | 2 | a0001c0001t0006g0108 a0001c0001t0006g0109 |
2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.445+13641T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640433 | |||||||
| chr13:23640459 | G | A | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445+13667G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640459 | |||||||
| chr13:23640464 | G | A | 78 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445+13672G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640464 | |||||||
| chr13:23640518 | C | A | 78 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(75): Show |
82 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.445+13726C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640518 | |||||||
| chr13:23640628 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.445+13836T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640628 | |||||||
| chr13:23640674 | A | G | 91 | a0001c0001t0001g0158 a0001c0001t0001g0191 a0001c0001t0003g0012 others(88): Show |
95 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.445+13882A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640674 | |||||||
| chr13:23640886 | T | C | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.445+14094T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23640886 | |||||||
| chr13:23641043 | T | A | 1 | a0002c0002t0001g0129 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.445+14251T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641043 | |||||||
| chr13:23641097 | T | A | 65 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(62): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.445+14305T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641097 | |||||||
| chr13:23641219 | C | T | 1 | a0004c0006t0013g0371 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.445+14427C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641219 | |||||||
| chr13:23641226 | C | T | 10 | a0003c0003t0001g0251 a0003c0003t0001g0254 a0003c0003t0001g0263 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.445+14434C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641226 | |||||||
| chr13:23641320 | T | C | 1 | a0002c0002t0005g0349 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.445+14528T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641320 | |||||||
| chr13:23641505 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0062 others(66): Show |
73 | HG00438.hp2 HG00609.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.445+14713A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641505 | |||||||
| chr13:23641546 | G | A | 3 | a0005c0008t0007g0029 a0005c0008t0007g0030 a0005c0008t0007g0184 |
3 | HG01496.hp1 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.445+14754G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641546 | |||||||
| chr13:23641570 | A | G | 3 | a0001c0004t0002g0188 a0001c0004t0002g0210 a0001c0004t0002g0211 |
3 | NA19060.hp2 NA19085.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.445+14778A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641570 | |||||||
| chr13:23641713 | C | T | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.445+14921C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641713 | |||||||
| chr13:23641873 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0062 others(215): Show |
228 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.445+15081A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641873 | |||||||
| chr13:23641894 | C | A | 79 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.445+15102C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641894 | |||||||
| chr13:23641919 | T | C | 3 | a0002c0002t0005g0353 a0002c0002t0005g0368 a0002c0002t0005g0370 |
3 | NA18979.hp1 NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.445+15127T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23641919 | |||||||
| chr13:23642031 | C | T | 4 | a0002c0002t0001g0123 a0002c0002t0001g0244 a0002c0002t0001g0246 others(1): Show |
4 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+15239C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642031 | |||||||
| chr13:23642165 | T | C | 1 | a0001c0001t0001g0327 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.445+15373T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642165 | |||||||
| chr13:23642169 | A | G | 1 | a0002c0005t0002g0087 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.445+15377A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642169 | |||||||
| chr13:23642174 | T | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 |
3 | HG01167.hp2 HG03669.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.445+15382T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642174 | |||||||
| chr13:23642281 | T | C | 2 | a0003c0003t0001g0318 a0004c0006t0001g0041 |
2 | HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.445+15489T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642281 | |||||||
| chr13:23642816 | T | A | 79 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.445+16024T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642816 | |||||||
| chr13:23642828 | A | G | 12 | a0001c0001t0027g0223 a0001c0004t0025g0345 a0001c0004t0036g0221 others(9): Show |
12 | HG00738.hp2 HG01074.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.445+16036A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642828 | |||||||
| chr13:23642953 | C | T | 79 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(76): Show |
83 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.446-16097C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642953 | |||||||
| chr13:23642963 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.446-16087G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23642963 | |||||||
| chr13:23643021 | A | C | 6 | a0001c0004t0002g0173 a0001c0007t0011g0164 a0001c0007t0011g0165 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.446-16029A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23643021 | |||||||
| chr13:23643062 | G | A | 1 | a0002c0002t0005g0347 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.446-15988G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23643062 | |||||||
| chr13:23643262 | C | T | 1 | a0002c0002t0001g0123 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.446-15788C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23643262 | |||||||
| chr13:23643461 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446-15589T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23643461 | |||||||
| chr13:23643621 | AAC | A | 7 | a0005c0008t0007g0019 a0005c0008t0007g0022 a0005c0008t0007g0029 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-15423_446-1542 others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23643621 | ||||||
| chr13:23643724 | C | T | 4 | a0002c0002t0015g0023 a0002c0002t0015g0026 a0002c0002t0015g0031 others(1): Show |
4 | HG02257.hp1 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-15326C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23643724 | |||||||
| chr13:23643935 | G | C | 1 | a0002c0005t0002g0085 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.446-15115G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23643935 | |||||||
| chr13:23644048 | A | G | 1 | a0004c0006t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.446-15002A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23644048 | |||||||
| chr13:23644071 | T | C | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.446-14979T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23644071 | |||||||
| chr13:23644095 | A | G | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.446-14955A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23644095 | |||||||
| chr13:23644274 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.446-14776C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23644274 | |||||||
| chr13:23644300 | G | T | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.446-14750G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23644300 | |||||||
| chr13:23644366 | A | T | 5 | a0001c0007t0030g0331 a0002c0002t0015g0023 a0002c0002t0015g0026 others(2): Show |
5 | HG02257.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.446-14684A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23644366 | |||||||
| chr13:23644478 | C | G | 1 | a0001c0007t0001g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.446-14572C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23644478 | |||||||
| chr13:23644677 | T | C | 12 | a0001c0001t0027g0223 a0001c0004t0025g0345 a0001c0004t0036g0221 others(9): Show |
12 | HG00738.hp2 HG01074.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.446-14373T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23644677 | |||||||
| chr13:23644831 | GTA | G | 366 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(363): Show |
381 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(378): Show |
intron_variant | MODIFIER | c.446-14205_446-1420 others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23644831 | ||||||
| chr13:23645062 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.446-13988T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645062 | |||||||
| chr13:23645091 | G | T | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-13959G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645091 | |||||||
| chr13:23645261 | C | T | 2 | a0002c0002t0001g0128 a0004c0006t0001g0021 |
2 | HG02559.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.446-13789C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645261 | |||||||
| chr13:23645284 | C | G | 66 | a0001c0001t0001g0158 a0001c0001t0001g0301 a0001c0001t0003g0012 others(63): Show |
69 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.446-13766C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645284 | |||||||
| chr13:23645316 | C | G | 7 | a0005c0008t0007g0019 a0005c0008t0007g0022 a0005c0008t0007g0029 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-13734C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645316 | |||||||
| chr13:23645351 | A | G | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-13699A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645351 | |||||||
| chr13:23645465 | G | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0045 others(58): Show |
64 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.446-13585G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645465 | |||||||
| chr13:23645543 | G | A | 2 | a0001c0001t0033g0190 a0002c0002t0001g0028 |
2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.446-13507G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645543 | |||||||
| chr13:23645578 | A | C | 3 | a0001c0004t0025g0345 a0002c0005t0012g0182 a0002c0005t0012g0183 |
3 | HG02647.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.446-13472A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645578 | |||||||
| chr13:23645820 | C | G | 10 | a0003c0003t0001g0251 a0003c0003t0001g0254 a0003c0003t0001g0263 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-13230C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645820 | |||||||
| chr13:23645821 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(165): Show |
175 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(172): Show |
intron_variant | MODIFIER | c.446-13229G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645821 | |||||||
| chr13:23645922 | C | T | 1 | a0002c0002t0003g0005 | 2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.446-13128C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23645922 | |||||||
| chr13:23646024 | C | T | 29 | a0001c0001t0001g0301 a0001c0001t0004g0004 a0001c0001t0004g0051 others(26): Show |
30 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.446-13026C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23646024 | |||||||
| chr13:23646135 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446-12915G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23646135 | |||||||
| chr13:23646261 | C | A | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.446-12789C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23646261 | |||||||
| chr13:23646382 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.446-12668T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23646382 | |||||||
| chr13:23646525 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.446-12525G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23646525 | |||||||
| chr13:23646633 | G | A | 7 | a0003c0003t0006g0159 a0003c0003t0006g0160 a0004c0006t0006g0025 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-12417G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23646633 | |||||||
| chr13:23646677 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(248): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.446-12373T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23646677 | |||||||
| chr13:23646696 | G | A | 1 | a0003c0003t0001g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.446-12354G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23646696 | |||||||
| chr13:23647052 | T | C | 1 | a0003c0003t0001g0310 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.446-11998T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647052 | |||||||
| chr13:23647054 | G | A | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-11996G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647054 | |||||||
| chr13:23647206 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0320 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.446-11844A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647206 | |||||||
| chr13:23647350 | T | C | 7 | a0005c0008t0007g0019 a0005c0008t0007g0022 a0005c0008t0007g0029 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-11700T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647350 | |||||||
| chr13:23647408 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0002c0002t0001g0042 |
3 | HG01243.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.446-11642A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647408 | |||||||
| chr13:23647415 | T | G | 8 | a0003c0003t0006g0159 a0003c0003t0006g0160 a0004c0006t0006g0025 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-11635T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647415 | |||||||
| chr13:23647527 | C | T | 2 | a0003c0003t0001g0318 a0004c0006t0001g0041 |
2 | HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.446-11523C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647527 | |||||||
| chr13:23647530 | G | C | 1 | a0003c0003t0001g0307 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.446-11520G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647530 | |||||||
| chr13:23647569 | AT | A | 8 | a0003c0003t0006g0159 a0003c0003t0006g0160 a0004c0006t0006g0025 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-11472delT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23647569 | ||||||
| chr13:23647867 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0166 a0001c0001t0001g0170 others(9): Show |
13 | HG00735.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-11183C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647867 | |||||||
| chr13:23647912 | G | C | 46 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(43): Show |
48 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.446-11138G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647912 | |||||||
| chr13:23647947 | T | C | 1 | a0001c0001t0003g0093 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.446-11103T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23647947 | |||||||
| chr13:23648055 | A | G | 1 | a0001c0001t0033g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.446-10995A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648055 | |||||||
| chr13:23648059 | T | G | 3 | a0001c0004t0025g0345 a0002c0005t0012g0182 a0002c0005t0012g0183 |
3 | HG02647.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.446-10991T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648059 | |||||||
| chr13:23648061 | A | G | 5 | a0001c0004t0002g0274 a0002c0005t0002g0046 a0002c0005t0005g0359 others(2): Show |
5 | HG02155.hp1 NA18943.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-10989A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648061 | |||||||
| chr13:23648129 | C | T | 2 | a0003c0003t0001g0263 a0003c0003t0001g0264 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.446-10921C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648129 | |||||||
| chr13:23648143 | C | A | 9 | a0003c0003t0001g0318 a0004c0006t0001g0041 a0005c0008t0007g0019 others(6): Show |
10 | HG00280.hp1 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-10907C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648143 | |||||||
| chr13:23648215 | A | G | 1 | a0002c0002t0003g0133 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.446-10835A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648215 | |||||||
| chr13:23648234 | C | A | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-10816C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648234 | |||||||
| chr13:23648377 | C | T | 1 | a0004c0006t0013g0371 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.446-10673C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648377 | |||||||
| chr13:23648440 | T | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0062 others(124): Show |
133 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.446-10610T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648440 | |||||||
| chr13:23648499 | G | A | 1 | a0002c0005t0012g0014 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.446-10551G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648499 | |||||||
| chr13:23648549 | C | A | 41 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(38): Show |
44 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.446-10501C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648549 | |||||||
| chr13:23648577 | T | A | 1 | a0001c0022t0016g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.446-10473T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648577 | |||||||
| chr13:23648631 | A | G | 60 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0045 others(57): Show |
63 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.446-10419A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648631 | |||||||
| chr13:23648735 | A | G | 4 | a0001c0012t0001g0096 a0001c0012t0001g0097 a0002c0010t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-10315A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648735 | |||||||
| chr13:23648765 | A | C | 2 | a0005c0008t0007g0019 a0005c0008t0007g0022 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.446-10285A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648765 | |||||||
| chr13:23648848 | T | C | 9 | a0003c0003t0001g0318 a0004c0006t0001g0041 a0005c0008t0007g0019 others(6): Show |
10 | HG00280.hp1 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-10202T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23648848 | |||||||
| chr13:23649141 | A | G | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-9909A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649141 | |||||||
| chr13:23649143 | T | C | 1 | a0001c0001t0013g0343 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.446-9907T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649143 | |||||||
| chr13:23649200 | T | C | 1 | a0010c0020t0004g0297 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.446-9850T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649200 | |||||||
| chr13:23649453 | T | G | 5 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0278 others(2): Show |
5 | HG00280.hp2 HG01099.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-9597T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649453 | |||||||
| chr13:23649520 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0062 others(205): Show |
218 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.446-9530C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649520 | |||||||
| chr13:23649605 | G | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0224 |
2 | HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.446-9445G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649605 | |||||||
| chr13:23649659 | T | G | 1 | a0001c0001t0013g0343 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.446-9391T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649659 | |||||||
| chr13:23649695 | A | G | 1 | a0003c0003t0006g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.446-9355A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649695 | |||||||
| chr13:23649718 | G | A | 1 | a0001c0004t0002g0279 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.446-9332G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649718 | |||||||
| chr13:23649905 | T | A | 1 | a0001c0001t0010g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.446-9145T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649905 | |||||||
| chr13:23649927 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.446-9123T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649927 | |||||||
| chr13:23649929 | C | A | 3 | a0002c0002t0015g0023 a0002c0002t0015g0026 a0002c0002t0015g0031 |
3 | HG02257.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.446-9121C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649929 | |||||||
| chr13:23649948 | G | A | 3 | a0002c0002t0001g0244 a0002c0002t0001g0246 a0002c0002t0001g0247 |
3 | HG01167.hp1 HG01169.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.446-9102G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649948 | |||||||
| chr13:23649965 | C | G | 71 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(68): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.446-9085C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23649965 | |||||||
| chr13:23650003 | C | T | 53 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(50): Show |
55 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.446-9047C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23650003 | |||||||
| chr13:23650033 | T | C | 5 | a0003c0003t0001g0230 a0003c0003t0001g0243 a0003c0003t0001g0289 others(2): Show |
5 | HG01255.hp2 HG01256.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.446-9017T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23650033 | |||||||
| chr13:23650428 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0320 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.446-8622G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23650428 | |||||||
| chr13:23650601 | G | T | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.446-8449G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23650601 | |||||||
| chr13:23650732 | A | G | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-8318A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23650732 | |||||||
| chr13:23650850 | C | T | 1 | a0001c0004t0002g0253 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.446-8200C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23650850 | |||||||
| chr13:23651000 | T | C | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-8050T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651000 | |||||||
| chr13:23651040 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.446-8010T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651040 | |||||||
| chr13:23651330 | T | C | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-7720T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651330 | |||||||
| chr13:23651378 | C | T | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.446-7672C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651378 | |||||||
| chr13:23651499 | A | G | 2 | a0002c0005t0012g0014 a0002c0005t0012g0015 |
2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.446-7551A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651499 | |||||||
| chr13:23651632 | A | T | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-7418A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651632 | |||||||
| chr13:23651719 | T | G | 1 | a0002c0002t0005g0349 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.446-7331T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651719 | |||||||
| chr13:23651825 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.446-7225C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651825 | |||||||
| chr13:23651840 | C | CT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0229 others(21): Show |
27 | HG00639.hp1 HG01243.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.446-7189dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651840 | ||||||
| chr13:23651840 | C | CTT | 58 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0045 others(55): Show |
62 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.446-7190_446-7189d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651840 | ||||||
| chr13:23651840 | C | CTTT | 67 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0001g0225 others(64): Show |
71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.446-7191_446-7189d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651840 | ||||||
| chr13:23651840 | C | CTTTT | 12 | a0001c0001t0003g0196 a0001c0001t0003g0255 a0001c0001t0004g0066 others(9): Show |
12 | HG00423.hp1 HG00673.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.446-7192_446-7189d others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651840 | ||||||
| chr13:23651893 | T | TA | 125 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0045 others(122): Show |
130 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.446-7134dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651893 | ||||||
| chr13:23651893 | T | TAA | 33 | a0001c0001t0001g0323 a0001c0001t0003g0091 a0001c0001t0004g0004 others(30): Show |
34 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.446-7135_446-7134d others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651893 | ||||||
| chr13:23651893 | T | TAAA | 39 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(36): Show |
42 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.446-7136_446-7134d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651893 | ||||||
| chr13:23651893 | T | TAAAA | 6 | a0001c0001t0003g0341 a0001c0001t0008g0053 a0001c0001t0008g0262 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.446-7137_446-7134d others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651893 | ||||||
| chr13:23651893 | T | TAAAAA | 9 | a0001c0007t0030g0331 a0002c0002t0015g0023 a0005c0008t0007g0019 others(6): Show |
10 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-7138_446-7134d others(7): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651893 | ||||||
| chr13:23651893 | TA | T | 8 | a0001c0001t0001g0212 a0001c0001t0027g0223 a0001c0004t0025g0345 others(5): Show |
8 | HG01361.hp2 HG02683.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.446-7134delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23651893 | ||||||
| chr13:23651919 | A | G | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.446-7131A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23651919 | |||||||
| chr13:23652010 | T | C | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.446-7040T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23652010 | |||||||
| chr13:23652179 | C | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0062 others(134): Show |
142 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.446-6871C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23652179 | |||||||
| chr13:23652489 | G | A | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-6561G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23652489 | |||||||
| chr13:23652543 | G | C | 71 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(68): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.446-6507G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23652543 | |||||||
| chr13:23652643 | C | T | 1 | a0003c0003t0022g0008 | 2 | NA18950.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.446-6407C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23652643 | |||||||
| chr13:23652694 | G | A | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.446-6356G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23652694 | |||||||
| chr13:23652842 | G | A | 3 | a0002c0005t0002g0118 a0002c0005t0002g0136 a0002c0005t0002g0328 |
3 | NA18948.hp2 NA19086.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.446-6208G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23652842 | |||||||
| chr13:23652868 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.446-6182C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23652868 | |||||||
| chr13:23653401 | C | A | 1 | a0001c0001t0004g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.446-5649C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23653401 | |||||||
| chr13:23653414 | G | A | 1 | a0001c0001t0013g0343 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.446-5636G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23653414 | |||||||
| chr13:23653489 | G | A | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-5561G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23653489 | |||||||
| chr13:23653830 | C | T | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.446-5220C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23653830 | |||||||
| chr13:23653842 | A | G | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-5208A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23653842 | |||||||
| chr13:23653914 | G | C | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.446-5136G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23653914 | |||||||
| chr13:23653976 | C | T | 1 | a0001c0001t0008g0287 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.446-5074C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23653976 | |||||||
| chr13:23653980 | C | T | 2 | a0002c0002t0015g0023 a0002c0002t0015g0031 |
2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.446-5070C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23653980 | |||||||
| chr13:23654064 | G | A | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-4986G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23654064 | |||||||
| chr13:23654490 | C | G | 1 | a0002c0002t0010g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.446-4560C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23654490 | |||||||
| chr13:23654532 | C | T | 7 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(4): Show |
7 | NA18941.hp2 NA18946.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.446-4518C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23654532 | |||||||
| chr13:23654832 | C | T | 1 | a0001c0022t0016g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.446-4218C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23654832 | |||||||
| chr13:23654875 | G | A | 71 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(68): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.446-4175G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23654875 | |||||||
| chr13:23654907 | C | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(292): Show |
308 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.446-4143C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23654907 | |||||||
| chr13:23654936 | A | G | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0002c0002t0001g0042 others(2): Show |
5 | HG01243.hp2 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.446-4114A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23654936 | |||||||
| chr13:23655120 | T | C | 1 | a0001c0001t0003g0311 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.446-3930T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655120 | |||||||
| chr13:23655186 | A | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(292): Show |
308 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.446-3864A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655186 | |||||||
| chr13:23655195 | T | C | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.446-3855T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655195 | |||||||
| chr13:23655214 | G | A | 83 | a0001c0001t0001g0095 a0001c0001t0001g0158 a0001c0001t0003g0012 others(80): Show |
88 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.446-3836G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655214 | |||||||
| chr13:23655228 | C | A | 1 | a0001c0001t0003g0231 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.446-3822C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655228 | |||||||
| chr13:23655238 | A | G | 2 | a0001c0001t0027g0223 a0001c0007t0001g0163 |
2 | HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.446-3812A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655238 | |||||||
| chr13:23655398 | G | A | 71 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(68): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.446-3652G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655398 | |||||||
| chr13:23655655 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446-3395C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655655 | |||||||
| chr13:23655738 | GC | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(320): Show |
338 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.446-3302delC | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23655738 | ||||||
| chr13:23655816 | T | A | 2 | a0003c0003t0001g0263 a0003c0003t0001g0264 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.446-3234T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655816 | |||||||
| chr13:23655920 | A | C | 9 | a0003c0003t0001g0300 a0003c0003t0001g0325 a0003c0003t0022g0008 others(6): Show |
10 | HG00408.hp1 HG00438.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-3130A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655920 | |||||||
| chr13:23655932 | G | A | 1 | a0002c0017t0011g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.446-3118G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23655932 | |||||||
| chr13:23656053 | A | G | 1 | a0002c0002t0010g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.446-2997A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656053 | |||||||
| chr13:23656303 | C | T | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-2747C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656303 | |||||||
| chr13:23656429 | G | A | 2 | a0002c0010t0001g0016 a0002c0010t0001g0152 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.446-2621G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656429 | |||||||
| chr13:23656494 | A | G | 71 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(68): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.446-2556A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656494 | |||||||
| chr13:23656498 | A | C | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.446-2552A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656498 | |||||||
| chr13:23656575 | G | A | 1 | a0001c0004t0017g0205 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.446-2475G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656575 | |||||||
| chr13:23656663 | G | A | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.446-2387G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656663 | |||||||
| chr13:23656672 | G | C | 85 | a0001c0001t0001g0095 a0001c0001t0001g0158 a0001c0001t0003g0012 others(82): Show |
90 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.446-2378G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656672 | |||||||
| chr13:23656717 | C | G | 3 | a0002c0002t0015g0023 a0002c0002t0015g0026 a0002c0002t0015g0031 |
3 | HG02257.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.446-2333C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656717 | |||||||
| chr13:23656989 | A | T | 1 | a0001c0004t0002g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.446-2061A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23656989 | |||||||
| chr13:23657212 | C | T | 5 | a0001c0001t0003g0196 a0001c0001t0003g0311 a0001c0001t0003g0313 others(2): Show |
6 | HG00738.hp1 HG01074.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.446-1838C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23657212 | |||||||
| chr13:23657626 | G | T | 1 | a0002c0005t0005g0351 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.446-1424G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23657626 | |||||||
| chr13:23657643 | T | C | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-1407T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23657643 | |||||||
| chr13:23657680 | TTTC | T | 17 | a0001c0001t0001g0191 a0001c0001t0020g0330 a0001c0001t0020g0332 others(14): Show |
17 | HG01243.hp1 HG01361.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.446-1349_446-1347d others(5): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 23657680 | ||||||
| chr13:23657701 | C | T | 16 | a0001c0001t0001g0191 a0001c0001t0020g0330 a0001c0001t0020g0332 others(13): Show |
16 | HG01243.hp1 HG01361.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.446-1349C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23657701 | |||||||
| chr13:23657862 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.446-1188C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23657862 | |||||||
| chr13:23657972 | G | T | 2 | a0001c0001t0033g0190 a0002c0002t0001g0028 |
2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.446-1078G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23657972 | |||||||
| chr13:23657974 | C | T | 1 | a0001c0001t0004g0063 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.446-1076C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23657974 | |||||||
| chr13:23658044 | C | A | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.446-1006C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658044 | |||||||
| chr13:23658146 | T | C | 4 | a0005c0008t0007g0029 a0005c0008t0007g0030 a0005c0008t0007g0184 others(1): Show |
5 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.446-904T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658146 | |||||||
| chr13:23658151 | A | G | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.446-899A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658151 | |||||||
| chr13:23658254 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.446-796A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658254 | |||||||
| chr13:23658569 | A | G | 71 | a0001c0001t0001g0158 a0001c0001t0003g0012 a0001c0001t0003g0088 others(68): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.446-481A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658569 | |||||||
| chr13:23658588 | T | C | 1 | a0001c0001t0004g0078 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.446-462T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658588 | |||||||
| chr13:23658605 | C | A | 7 | a0005c0008t0007g0019 a0005c0008t0007g0022 a0005c0008t0007g0029 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-445C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658605 | |||||||
| chr13:23658709 | T | C | 3 | a0001c0001t0001g0191 a0001c0001t0027g0223 a0001c0007t0001g0163 |
3 | HG01361.hp2 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.446-341T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658709 | |||||||
| chr13:23658798 | G | A | 2 | a0001c0001t0027g0223 a0001c0007t0001g0163 |
2 | HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.446-252G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658798 | |||||||
| chr13:23658816 | G | A | 8 | a0003c0003t0006g0159 a0003c0003t0006g0160 a0003c0003t0006g0185 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.446-234G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658816 | |||||||
| chr13:23658851 | C | T | 1 | a0002c0005t0012g0017 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.446-199C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658851 | |||||||
| chr13:23658855 | T | C | 3 | a0001c0001t0003g0088 a0002c0002t0003g0135 a0002c0002t0003g0153 |
3 | HG03490.hp2 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.446-195T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658855 | |||||||
| chr13:23658990 | G | A | 1 | a0005c0008t0007g0184 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.446-60G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 5/9 | chr13 | 23658990 | |||||||
| chr13:23659631 | G | A | 3 | a0002c0002t0015g0023 a0002c0002t0015g0026 a0002c0002t0015g0031 |
3 | HG02257.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.610+417G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659631 | |||||||
| chr13:23659660 | C | T | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.610+446C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659660 | |||||||
| chr13:23659756 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.610+542C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659756 | |||||||
| chr13:23659799 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.611-566C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659799 | |||||||
| chr13:23659802 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(135): Show |
145 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.611-563C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659802 | |||||||
| chr13:23659822 | C | T | 4 | a0001c0012t0001g0096 a0001c0012t0001g0097 a0002c0010t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.611-543C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659822 | |||||||
| chr13:23659833 | C | T | 1 | a0002c0002t0013g0372 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.611-532C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659833 | |||||||
| chr13:23659904 | C | T | 1 | a0002c0002t0016g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.611-461C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659904 | |||||||
| chr13:23659918 | G | A | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0010t0001g0016 |
3 | HG02647.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.611-447G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23659918 | |||||||
| chr13:23660002 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(131): Show |
141 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.611-363C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23660002 | |||||||
| chr13:23660045 | C | T | 1 | a0001c0001t0004g0157 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.611-320C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23660045 | |||||||
| chr13:23660046 | G | A | 3 | a0002c0002t0015g0023 a0002c0002t0015g0026 a0002c0002t0015g0031 |
3 | HG02257.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.611-319G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23660046 | |||||||
| chr13:23660127 | G | A | 1 | a0001c0001t0006g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.611-238G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23660127 | |||||||
| chr13:23660230 | G | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(129): Show |
139 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.611-135G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23660230 | |||||||
| chr13:23660236 | A | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(129): Show |
139 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.611-129A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 6/9 | chr13 | 23660236 | |||||||
| chr13:23661051 | T | A | 1 | a0001c0004t0002g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.736+561T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661051 | |||||||
| chr13:23661118 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG00639.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.736+628C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661118 | |||||||
| chr13:23661162 | T | C | 6 | a0001c0007t0011g0164 a0001c0007t0011g0165 a0001c0007t0011g0193 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.736+672T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661162 | |||||||
| chr13:23661200 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.736+710C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661200 | |||||||
| chr13:23661323 | T | C | 64 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(61): Show |
66 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.736+833T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661323 | |||||||
| chr13:23661358 | C | A | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.736+868C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661358 | |||||||
| chr13:23661387 | G | A | 2 | a0001c0001t0033g0190 a0002c0002t0001g0028 |
2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.736+897G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661387 | |||||||
| chr13:23661553 | A | T | 151 | a0001c0001t0001g0095 a0001c0001t0001g0191 a0001c0001t0003g0012 others(148): Show |
157 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.736+1063A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661553 | |||||||
| chr13:23661771 | A | G | 1 | a0004c0006t0009g0361 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.736+1281A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661771 | |||||||
| chr13:23661821 | G | C | 6 | a0001c0004t0002g0002 a0001c0004t0002g0058 a0001c0004t0002g0194 others(3): Show |
8 | HG00621.hp2 HG02165.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.736+1331G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23661821 | |||||||
| chr13:23662025 | A | G | 1 | a0001c0001t0010g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.736+1535A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662025 | |||||||
| chr13:23662057 | A | G | 3 | a0002c0002t0015g0023 a0002c0002t0015g0026 a0002c0002t0015g0031 |
3 | HG02257.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.736+1567A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662057 | |||||||
| chr13:23662094 | T | A | 3 | a0002c0002t0015g0023 a0002c0002t0015g0026 a0002c0002t0015g0031 |
3 | HG02257.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.736+1604T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662094 | |||||||
| chr13:23662136 | T | C | 152 | a0001c0001t0001g0095 a0001c0001t0001g0191 a0001c0001t0003g0012 others(149): Show |
158 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+1646T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662136 | |||||||
| chr13:23662168 | T | C | 1 | a0001c0022t0016g0326 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.736+1678T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662168 | |||||||
| chr13:23662438 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.736+1948G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662438 | |||||||
| chr13:23662508 | A | G | 1 | a0003c0003t0001g0204 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.736+2018A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662508 | |||||||
| chr13:23662558 | T | A | 40 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(37): Show |
43 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.736+2068T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662558 | |||||||
| chr13:23662610 | T | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(288): Show |
304 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.736+2120T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662610 | |||||||
| chr13:23662652 | A | G | 2 | a0001c0001t0027g0223 a0001c0007t0001g0163 |
2 | HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.736+2162A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662652 | |||||||
| chr13:23662751 | C | A | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.736+2261C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662751 | |||||||
| chr13:23662805 | T | G | 1 | a0001c0001t0004g0308 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.736+2315T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662805 | |||||||
| chr13:23662819 | G | T | 1 | a0001c0001t0001g0316 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.736+2329G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662819 | |||||||
| chr13:23662826 | T | C | 1 | a0001c0001t0034g0154 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.736+2336T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662826 | |||||||
| chr13:23662848 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.736+2358A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23662848 | |||||||
| chr13:23663046 | A | G | 1 | a0001c0007t0030g0331 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.736+2556A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663046 | |||||||
| chr13:23663096 | G | C | 2 | a0004c0006t0001g0117 a0004c0006t0032g0140 |
2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.736+2606G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663096 | |||||||
| chr13:23663102 | A | G | 6 | a0001c0007t0011g0164 a0001c0007t0011g0165 a0001c0007t0011g0193 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.736+2612A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663102 | |||||||
| chr13:23663119 | C | A | 2 | a0001c0001t0027g0223 a0001c0007t0001g0163 |
2 | HG01361.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.736+2629C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663119 | |||||||
| chr13:23663211 | G | C | 7 | a0005c0008t0007g0019 a0005c0008t0007g0022 a0005c0008t0007g0029 others(4): Show |
8 | HG00280.hp1 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.736+2721G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663211 | |||||||
| chr13:23663313 | G | A | 1 | a0002c0002t0015g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.736+2823G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663313 | |||||||
| chr13:23663377 | G | A | 2 | a0002c0005t0012g0182 a0002c0005t0012g0183 |
2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.736+2887G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663377 | |||||||
| chr13:23663443 | T | C | 2 | a0001c0001t0010g0155 a0002c0002t0026g0105 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.736+2953T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663443 | |||||||
| chr13:23663515 | A | G | 55 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0045 others(52): Show |
58 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.736+3025A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663515 | |||||||
| chr13:23663696 | C | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(280): Show |
296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.736+3206C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663696 | |||||||
| chr13:23663915 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.736+3425C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663915 | |||||||
| chr13:23663982 | A | G | 1 | a0003c0003t0006g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.736+3492A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23663982 | |||||||
| chr13:23664058 | G | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0172 a0001c0001t0001g0219 |
3 | HG01167.hp2 HG03669.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.736+3568G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23664058 | |||||||
| chr13:23664059 | T | C | 2 | a0002c0005t0012g0014 a0002c0005t0012g0015 |
2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.736+3569T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23664059 | |||||||
| chr13:23664104 | T | C | 72 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(69): Show |
76 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.736+3614T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23664104 | |||||||
| chr13:23664153 | C | T | 1 | a0001c0013t0003g0260 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.736+3663C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23664153 | |||||||
| chr13:23664463 | C | T | 8 | a0003c0003t0006g0159 a0003c0003t0006g0160 a0003c0003t0006g0185 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.737-3517C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23664463 | |||||||
| chr13:23664472 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.737-3508A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23664472 | |||||||
| chr13:23664522 | C | T | 3 | a0001c0001t0003g0311 a0001c0001t0003g0313 a0001c0001t0003g0315 |
3 | HG01261.hp2 HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.737-3458C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23664522 | |||||||
| chr13:23664742 | A | T | 1 | a0001c0007t0001g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.737-3238A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23664742 | |||||||
| chr13:23665026 | G | C | 81 | a0001c0001t0001g0095 a0001c0001t0003g0012 a0001c0001t0003g0088 others(78): Show |
85 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.737-2954G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23665026 | |||||||
| chr13:23665527 | A | G | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.737-2453A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23665527 | |||||||
| chr13:23665552 | A | G | 2 | a0002c0005t0012g0014 a0002c0005t0012g0015 |
2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.737-2428A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23665552 | |||||||
| chr13:23665583 | C | CAT | 298 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(295): Show |
311 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.737-2397_737-2396i others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23665583 | |||||||
| chr13:23665686 | A | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(302): Show |
318 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.737-2294A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23665686 | |||||||
| chr13:23665773 | G | C | 9 | a0003c0003t0006g0159 a0003c0003t0006g0160 a0003c0003t0006g0185 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.737-2207G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23665773 | |||||||
| chr13:23665792 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0002c0002t0001g0042 |
3 | HG01243.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.737-2188A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23665792 | |||||||
| chr13:23665991 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.737-1989A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23665991 | |||||||
| chr13:23666012 | T | C | 95 | a0001c0001t0001g0095 a0001c0001t0001g0191 a0001c0001t0003g0012 others(92): Show |
100 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.737-1968T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666012 | |||||||
| chr13:23666070 | T | C | 4 | a0001c0001t0034g0154 a0002c0002t0015g0023 a0002c0002t0015g0026 others(1): Show |
4 | HG02257.hp1 HG02717.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-1910T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666070 | |||||||
| chr13:23666146 | A | G | 70 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(67): Show |
74 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.737-1834A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666146 | |||||||
| chr13:23666157 | G | C | 1 | a0001c0001t0004g0157 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.737-1823G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666157 | |||||||
| chr13:23666192 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(140): Show |
150 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.737-1788C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666192 | |||||||
| chr13:23666212 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.737-1768A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666212 | |||||||
| chr13:23666231 | T | C | 3 | a0001c0001t0001g0191 a0001c0001t0010g0155 a0002c0002t0026g0105 |
3 | HG01243.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737-1749T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666231 | |||||||
| chr13:23666289 | G | A | 2 | a0001c0001t0010g0155 a0002c0002t0026g0105 |
2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737-1691G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666289 | |||||||
| chr13:23666365 | T | G | 30 | a0001c0001t0004g0004 a0001c0001t0004g0051 a0001c0001t0004g0055 others(27): Show |
31 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.737-1615T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666365 | |||||||
| chr13:23666517 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.737-1463T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666517 | |||||||
| chr13:23666592 | A | G | 70 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(67): Show |
74 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.737-1388A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666592 | |||||||
| chr13:23666622 | T | C | 1 | a0002c0005t0014g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.737-1358T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666622 | |||||||
| chr13:23666670 | C | A | 1 | a0001c0007t0028g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.737-1310C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666670 | |||||||
| chr13:23666730 | C | T | 1 | a0001c0001t0003g0091 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.737-1250C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23666730 | |||||||
| chr13:23667068 | T | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0062 others(60): Show |
66 | HG00438.hp2 HG00609.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.737-912T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667068 | |||||||
| chr13:23667068 | T | TTG | 15 | a0001c0001t0008g0053 a0001c0001t0010g0155 a0001c0001t0027g0223 others(12): Show |
15 | HG01361.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.737-895_737-894dup others(2): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667068 | ||||||
| chr13:23667077 | T | C | 70 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(67): Show |
72 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.737-903T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667077 | |||||||
| chr13:23667120 | G | GAT | 4 | a0001c0001t0001g0212 a0001c0004t0002g0211 a0003c0003t0006g0159 others(1): Show |
4 | HG02258.hp1 HG02683.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-841_737-840dup others(2): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667120 | ||||||
| chr13:23667120 | G | GATAT | 9 | a0003c0003t0001g0230 a0003c0003t0006g0185 a0004c0006t0001g0103 others(6): Show |
9 | HG00438.hp1 HG01256.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.737-843_737-840dup others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667120 | ||||||
| chr13:23667120 | G | GATATAT | 42 | a0001c0001t0001g0191 a0003c0003t0001g0047 a0003c0003t0001g0048 others(39): Show |
43 | HG00639.hp1 HG00673.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.737-845_737-840dup others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667120 | ||||||
| chr13:23667120 | G | GATATATA others(1): Show |
10 | a0003c0003t0001g0083 a0003c0003t0001g0300 a0003c0003t0001g0302 others(7): Show |
11 | HG02015.hp1 HG02129.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.737-847_737-840dup others(8): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667120 | ||||||
| chr13:23667120 | G | GATATATA others(3): Show |
3 | a0003c0003t0001g0291 a0004c0006t0001g0102 a0004c0006t0009g0365 |
3 | HG02080.hp1 HG02129.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.737-849_737-840dup others(10): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667120 | ||||||
| chr13:23667120 | G | GATATATA others(5): Show |
1 | a0003c0003t0001g0325 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.737-851_737-840dup others(12): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667120 | ||||||
| chr13:23667120 | G | GATATATA others(7): Show |
1 | a0004c0006t0002g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.737-853_737-840dup others(14): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667120 | ||||||
| chr13:23667135 | ATATATG | A | 83 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(80): Show |
87 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.737-841_737-836del others(6): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667135 | ||||||
| chr13:23667137 | ATATG | A | 18 | a0001c0001t0034g0154 a0001c0004t0025g0345 a0001c0004t0036g0221 others(15): Show |
19 | HG00280.hp1 HG00738.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-835_737-832del others(4): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667137 | ||||||
| chr13:23667139 | ATG | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(103): Show |
112 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.737-839_737-838del others(2): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667139 | ||||||
| chr13:23667141 | G | A | 91 | a0001c0001t0001g0158 a0001c0001t0001g0167 a0001c0001t0001g0168 others(88): Show |
93 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.737-839G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667141 | |||||||
| chr13:23667313 | T | C | 8 | a0001c0001t0004g0055 a0001c0001t0004g0061 a0001c0001t0004g0064 others(5): Show |
8 | HG02083.hp1 NA18953.hp1 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.737-667T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667313 | |||||||
| chr13:23667357 | A | G | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.737-623A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667357 | |||||||
| chr13:23667472 | C | T | 40 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(37): Show |
43 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.737-508C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667472 | |||||||
| chr13:23667483 | C | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0002c0002t0001g0042 |
3 | HG01243.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.737-497C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667483 | |||||||
| chr13:23667579 | A | G | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.737-401A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667579 | |||||||
| chr13:23667618 | G | A | 1 | a0001c0012t0001g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.737-362G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667618 | |||||||
| chr13:23667690 | A | T | 55 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0045 others(52): Show |
58 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.737-290A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667690 | |||||||
| chr13:23667717 | C | CA | 3 | a0001c0004t0017g0205 a0001c0004t0017g0240 a0001c0004t0017g0242 |
3 | HG02056.hp1 NA18939.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.737-262dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 23667717 | ||||||
| chr13:23667726 | G | T | 68 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(65): Show |
70 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.737-254G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667726 | |||||||
| chr13:23667877 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.737-103C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667877 | |||||||
| chr13:23667884 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(281): Show |
297 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.737-96A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 7/9 | chr13 | 23667884 | |||||||
| chr13:23668373 | T | A | 72 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(69): Show |
74 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.839+291T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 8/9 | chr13 | 23668373 | |||||||
| chr13:23668457 | T | C | 6 | a0001c0001t0027g0223 a0002c0002t0010g0013 a0002c0002t0010g0018 others(3): Show |
6 | HG01361.hp2 HG02630.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.840-235T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 8/9 | chr13 | 23668457 | |||||||
| chr13:23668510 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(113): Show |
122 | HG00323.hp1 HG00438.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.840-182A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 8/9 | chr13 | 23668510 | |||||||
| chr13:23668662 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(280): Show |
296 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.840-30A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 8/9 | chr13 | 23668662 | |||||||
| chr13:23669191 | G | GT | 62 | a0001c0001t0003g0296 a0002c0005t0005g0369 a0003c0003t0001g0047 others(59): Show |
64 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.1245+104dupT | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 23669191 | ||||||
| chr13:23669192 | T | G | 1 | a0002c0002t0013g0372 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1245+95T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669192 | |||||||
| chr13:23669221 | G | A | 70 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(67): Show |
74 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1245+124G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669221 | |||||||
| chr13:23669266 | A | T | 72 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(69): Show |
74 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1245+169A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669266 | |||||||
| chr13:23669288 | A | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(271): Show |
287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1245+191A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669288 | |||||||
| chr13:23669552 | T | C | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1245+455T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669552 | |||||||
| chr13:23669561 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1245+464C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669561 | |||||||
| chr13:23669582 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(291): Show |
307 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.1245+485T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669582 | |||||||
| chr13:23669844 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1245+747T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669844 | |||||||
| chr13:23669846 | A | C | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1245+749A>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669846 | |||||||
| chr13:23669847 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1245+750A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669847 | |||||||
| chr13:23669850 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1245+753G>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669850 | |||||||
| chr13:23669854 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(292): Show |
308 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.1245+757T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669854 | |||||||
| chr13:23669855 | G | A | 63 | a0001c0001t0001g0075 a0003c0003t0001g0047 a0003c0003t0001g0048 others(60): Show |
65 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1245+758G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669855 | |||||||
| chr13:23669856 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1245+759C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669856 | |||||||
| chr13:23669857 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1245+760A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23669857 | |||||||
| chr13:23670234 | G | A | 1 | a0002c0005t0002g0328 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1245+1137G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23670234 | |||||||
| chr13:23670280 | G | A | 1 | a0003c0003t0001g0197 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1245+1183G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23670280 | |||||||
| chr13:23670414 | C | G | 2 | a0002c0002t0003g0133 a0002c0002t0003g0150 |
2 | NA19007.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1245+1317C>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23670414 | |||||||
| chr13:23670554 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1245+1457T>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23670554 | |||||||
| chr13:23670561 | A | T | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1245+1464A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23670561 | |||||||
| chr13:23670653 | C | T | 3 | a0001c0001t0003g0255 a0001c0001t0003g0258 a0001c0001t0043g0178 |
3 | HG01175.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1245+1556C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23670653 | |||||||
| chr13:23670659 | A | G | 5 | a0001c0004t0002g0080 a0001c0004t0002g0081 a0002c0005t0005g0351 others(2): Show |
5 | HG00621.hp1 NA18995.hp1 NA19088.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245+1562A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23670659 | |||||||
| chr13:23670755 | C | T | 63 | a0001c0001t0001g0319 a0003c0003t0001g0047 a0003c0003t0001g0048 others(60): Show |
65 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1245+1658C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23670755 | |||||||
| chr13:23671007 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(278): Show |
294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.1245+1910G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671007 | |||||||
| chr13:23671189 | C | T | 4 | a0001c0007t0011g0164 a0001c0007t0011g0165 a0001c0007t0011g0193 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1245+2092C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671189 | |||||||
| chr13:23671215 | A | G | 1 | a0001c0007t0001g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1245+2118A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671215 | |||||||
| chr13:23671309 | A | G | 70 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(67): Show |
74 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1246-2063A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671309 | |||||||
| chr13:23671338 | A | G | 72 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(69): Show |
74 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1246-2034A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671338 | |||||||
| chr13:23671350 | G | A | 1 | a0002c0002t0026g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1246-2022G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671350 | |||||||
| chr13:23671362 | A | G | 1 | a0004c0006t0013g0371 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1246-2010A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671362 | |||||||
| chr13:23671507 | G | GA | 6 | a0002c0002t0006g0036 a0002c0002t0010g0013 a0002c0002t0010g0018 others(3): Show |
6 | HG02630.hp2 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1246-1853dupA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 23671507 | ||||||
| chr13:23671507 | GA | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(193): Show |
204 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.1246-1853delA | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 23671507 | ||||||
| chr13:23671535 | C | A | 70 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(67): Show |
74 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1246-1837C>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671535 | |||||||
| chr13:23671818 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02074.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1246-1554G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671818 | |||||||
| chr13:23671838 | A | G | 3 | a0001c0022t0016g0326 a0002c0002t0016g0039 a0002c0002t0016g0116 |
3 | HG02486.hp2 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1246-1534A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671838 | |||||||
| chr13:23671893 | CTCACTA | C | 72 | a0003c0003t0001g0047 a0003c0003t0001g0048 a0003c0003t0001g0050 others(69): Show |
74 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1246-1477_1246-147 others(10): Show |
TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 23671893 | ||||||
| chr13:23671959 | A | G | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1246-1413A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671959 | |||||||
| chr13:23671967 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1246-1405G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23671967 | |||||||
| chr13:23672010 | G | C | 1 | a0001c0001t0027g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1246-1362G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23672010 | |||||||
| chr13:23672274 | G | A | 1 | a0001c0001t0033g0190 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1246-1098G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23672274 | |||||||
| chr13:23672761 | G | A | 1 | a0002c0002t0001g0038 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1246-611G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23672761 | |||||||
| chr13:23672802 | T | C | 3 | a0001c0022t0016g0326 a0002c0002t0016g0039 a0002c0002t0016g0116 |
3 | HG02486.hp2 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1246-570T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23672802 | |||||||
| chr13:23672821 | C | T | 4 | a0001c0001t0008g0010 a0001c0001t0008g0261 a0001c0001t0008g0262 others(1): Show |
5 | NA18957.hp2 NA18981.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1246-551C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23672821 | |||||||
| chr13:23672836 | G | C | 1 | a0001c0001t0010g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1246-536G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23672836 | |||||||
| chr13:23672955 | A | T | 2 | a0001c0001t0020g0330 a0001c0001t0020g0332 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1246-417A>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23672955 | |||||||
| chr13:23673046 | G | C | 69 | a0001c0001t0003g0012 a0001c0001t0003g0088 a0001c0001t0003g0091 others(66): Show |
73 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1246-326G>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23673046 | |||||||
| chr13:23673111 | A | G | 3 | a0001c0001t0020g0330 a0001c0001t0020g0332 a0002c0002t0026g0105 |
3 | HG01243.hp1 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1246-261A>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23673111 | |||||||
| chr13:23673120 | G | A | 2 | a0002c0005t0005g0346 a0002c0005t0005g0367 |
2 | NA18942.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1246-252G>A | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23673120 | |||||||
| chr13:23673160 | C | T | 7 | a0001c0007t0011g0164 a0001c0007t0011g0165 a0001c0007t0011g0193 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1246-212C>T | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23673160 | |||||||
| chr13:23673271 | T | G | 1 | a0001c0004t0036g0221 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1246-101T>G | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23673271 | |||||||
| chr13:23673274 | T | C | 1 | a0002c0002t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1246-98T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23673274 | |||||||
| chr13:23673306 | T | C | 1 | a0001c0007t0011g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1246-66T>C | TNFRSF19 | ENSG00000127863.16 | transcript | ENST00000248484.9 | protein_coding | 9/9 | chr13 | 23673306 |