Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84910 |
| ensemblid | ENSG00000153214.11 |
| hgncid | 25913 |
| symbol | TMEM87B |
| name | transmembrane protein 87B |
| refseq_nuc | NM_032824.3 |
| refseq_prot | NP_116213.1 |
| ensembl_nuc | ENST00000283206.9 |
| ensembl_prot | ENSP00000283206.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 112055269 |
| end | 112119314 |
| strand | + |
| ver | v1.2 |
| region | chr2:112055269-112119314 |
| region5000 | chr2:112050269-112124314 |
| regionname0 | TMEM87B_chr2_112055269_112119314 |
| regionname5000 | TMEM87B_chr2_112050269_112124314 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 555 | 233 | 59 | 51 | 86 | 7 | 28 | 63 | TMEM87B_chr2_112050269_112124314 | TMEM87B | MVAAC others(550): Show |
chr2 | 112050269 | 112124314 |
| a0002 | 0/0 | 554 | 77 | 23 | 17 | 22 | 7 | 8 | 21 | TMEM87B_chr2_112050269_112124314 | TMEM87B | MVAAC others(549): Show |
chr2 | 112050269 | 112124314 |
| a0003 | 0/0 | 555 | 6 | 0 | 2 | 0 | 2 | 2 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | MVAAC others(550): Show |
chr2 | 112050269 | 112124314 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1665 | 228 | 55 | 50 | 86 | 7 | 28 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATGGT others(1660): Show |
chr2 | 112050269 | 112124314 | ||
| a0001c0004 | 0/0 | 1665 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATGGT others(1660): Show |
chr2 | 112050269 | 112124314 | ||
| a0001c0005 | 0/0 | 1665 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATGGT others(1660): Show |
chr2 | 112050269 | 112124314 | ||
| a0002c0002 | 0/0 | 1662 | 77 | 23 | 17 | 22 | 7 | 8 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATGGT others(1657): Show |
chr2 | 112050269 | 112124314 | ||
| a0003c0003 | 0/0 | 1665 | 6 | 0 | 2 | 0 | 2 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATGGT others(1660): Show |
chr2 | 112050269 | 112124314 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5162 | 84 | 15 | 14 | 48 | 1 | 6 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0002 | 1/1 | 5162 | 80 | 3 | 30 | 24 | 4 | 17 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0003 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0004 | 0/0 | 5162 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0005 | 0/0 | 5163 | 15 | 13 | 2 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5158): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0006 | 0/0 | 5162 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0007 | 0/0 | 5163 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5158): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0011 | 0/0 | 5162 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0013 | 0/0 | 5163 | 3 | 0 | 0 | 0 | 2 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5158): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0015 | 0/0 | 5162 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0017 | 0/0 | 5162 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0019 | 0/0 | 5162 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0021 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0022 | 0/0 | 5162 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0023 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0024 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5158): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0025 | 0/0 | 5162 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0026 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5158): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0027 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5158): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0028 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0029 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0030 | 0/0 | 5162 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0031 | 0/0 | 5162 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0032 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0033 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0034 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0035 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0036 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0037 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0038 | 0/0 | 5162 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0039 | 0/0 | 5161 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5156): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0040 | 0/0 | 5162 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0001t0042 | 0/0 | 5163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5158): Show |
chr2 | 112050269 | 112124314 |
| a0001c0004t0010 | 0/0 | 5162 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0001c0005t0020 | 0/0 | 5162 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0001 | 0/0 | 5159 | 4 | 2 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5154): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0003 | 0/0 | 5159 | 40 | 5 | 4 | 20 | 5 | 6 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5154): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0004 | 0/0 | 5159 | 17 | 11 | 5 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5154): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0008 | 0/0 | 5158 | 5 | 0 | 2 | 0 | 1 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5153): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0012 | 0/0 | 5159 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5154): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0014 | 0/0 | 5158 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5153): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0018 | 0/0 | 5159 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5154): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0041 | 0/0 | 5159 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5154): Show |
chr2 | 112050269 | 112124314 |
| a0002c0002t0043 | 0/0 | 5159 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5154): Show |
chr2 | 112050269 | 112124314 |
| a0003c0003t0009 | 0/0 | 5163 | 4 | 0 | 2 | 0 | 0 | 2 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5158): Show |
chr2 | 112050269 | 112124314 |
| a0003c0003t0016 | 0/0 | 5162 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | ATCTT others(5157): Show |
chr2 | 112050269 | 112124314 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0003 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0013g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0013g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0013g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0017g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0019g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0019g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0021g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0022g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0023g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0024g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0025g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0026g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0027g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0028g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0029g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0030g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0031g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0032g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0033g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0034g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0035g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0036g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0037g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0038g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0039g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0040g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0001t0042g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0004t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0004t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0004t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0004t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0001c0005t0020g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0008g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0008g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0012g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0014g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0014g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0014g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0018g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0018g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0041g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0002c0002t0043g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0003c0003t0009g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0003c0003t0009g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0003c0003t0009g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0003c0003t0016g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| a0003c0003t0016g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0063 | EUR | GBR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0159 | EUR | GBR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00140 | hp1 | a0002 | c0002 | t0003 | g0136 | EUR | GBR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | GBR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0241 | EUR | FIN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00323 | hp1 | a0002 | c0002 | t0004 | g0122 | EUR | FIN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0283 | EUR | FIN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00408 | hp2 | a0001 | c0001 | t0023 | g0057 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00438 | hp1 | a0001 | c0001 | t0038 | g0192 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00621 | hp2 | a0001 | c0001 | t0032 | g0210 | EAS | CHS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0261 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00639 | hp2 | a0002 | c0002 | t0004 | g0116 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00642 | hp2 | a0001 | c0001 | t0030 | g0054 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00738 | hp2 | a0002 | c0002 | t0004 | g0120 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00741 | hp1 | a0002 | c0002 | t0003 | g0166 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01069 | hp1 | a0002 | c0002 | t0003 | g0135 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01070 | hp2 | a0003 | c0003 | t0009 | g0013 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0134 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01074 | hp2 | a0002 | c0002 | t0014 | g0151 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01081 | hp1 | a0002 | c0002 | t0014 | g0152 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01099 | hp1 | a0002 | c0002 | t0014 | g0177 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01109 | hp1 | a0002 | c0002 | t0008 | g0154 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01109 | hp2 | a0001 | c0005 | t0020 | g0290 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01169 | hp1 | a0002 | c0002 | t0043 | g0156 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01175 | hp1 | a0002 | c0002 | t0004 | g0032 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0259 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0092 | AMR | PUR | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01255 | hp1 | a0002 | c0002 | t0008 | g0144 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01255 | hp2 | a0001 | c0001 | t0022 | g0067 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01256 | hp2 | a0002 | c0002 | t0004 | g0117 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01257 | hp1 | a0002 | c0002 | t0018 | g0292 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01258 | hp1 | a0002 | c0002 | t0004 | g0118 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01258 | hp2 | a0002 | c0002 | t0018 | g0291 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0149 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01346 | hp2 | a0003 | c0003 | t0009 | g0013 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01515 | hp1 | a0002 | c0002 | t0008 | g0007 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0006 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01516 | hp2 | a0003 | c0003 | t0016 | g0299 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01517 | hp1 | a0003 | c0003 | t0016 | g0300 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0006 | EUR | IBS | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01884 | hp1 | a0002 | c0002 | t0004 | g0024 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG01993 | hp2 | a0001 | c0001 | t0031 | g0080 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02015 | hp2 | a0001 | c0001 | t0034 | g0213 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0239 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0131 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0141 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0119 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02145 | hp2 | a0001 | c0001 | t0027 | g0296 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CDX | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02451 | hp1 | a0002 | c0002 | t0041 | g0277 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0231 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02572 | hp2 | a0002 | c0002 | t0004 | g0115 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0224 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0170 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0171 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02698 | hp2 | a0002 | c0002 | t0008 | g0007 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02723 | hp1 | a0001 | c0001 | t0035 | g0002 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02723 | hp2 | a0001 | c0001 | t0024 | g0019 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0037 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0158 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02809 | hp1 | a0002 | c0002 | t0004 | g0121 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02809 | hp2 | a0002 | c0002 | t0003 | g0169 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02895 | hp1 | a0002 | c0002 | t0012 | g0278 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02895 | hp2 | a0001 | c0004 | t0010 | g0288 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02896 | hp2 | a0001 | c0001 | t0042 | g0297 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02897 | hp2 | a0001 | c0004 | t0010 | g0289 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02922 | hp1 | a0001 | c0001 | t0011 | g0206 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02922 | hp2 | a0001 | c0004 | t0010 | g0287 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0230 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02970 | hp1 | a0002 | c0002 | t0012 | g0280 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03041 | hp2 | a0002 | c0002 | t0004 | g0200 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03098 | hp1 | a0001 | c0004 | t0010 | g0286 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03195 | hp1 | a0002 | c0002 | t0004 | g0132 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03195 | hp2 | a0001 | c0001 | t0033 | g0093 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03209 | hp1 | a0002 | c0002 | t0004 | g0294 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03209 | hp2 | a0002 | c0002 | t0004 | g0030 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0179 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03239 | hp2 | a0001 | c0001 | t0025 | g0111 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03453 | hp1 | a0001 | c0001 | t0026 | g0022 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0174 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0216 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03490 | hp2 | a0003 | c0003 | t0009 | g0298 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03491 | hp2 | a0002 | c0002 | t0003 | g0164 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0175 | AFR | ESN | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0091 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03654 | hp1 | a0003 | c0003 | t0009 | g0301 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03654 | hp2 | a0002 | c0002 | t0003 | g0160 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0284 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03704 | hp1 | a0002 | c0002 | t0008 | g0148 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03710 | hp2 | a0001 | c0001 | t0019 | g0168 | SAS | PJL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03942 | hp2 | a0001 | c0001 | t0019 | g0133 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0143 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0146 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | STU | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18522 | hp1 | a0001 | c0001 | t0036 | g0028 | AFR | YRI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18522 | hp2 | a0002 | c0002 | t0012 | g0281 | AFR | YRI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18906 | hp1 | a0002 | c0002 | t0012 | g0279 | AFR | YRI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | YRI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18939 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18941 | hp1 | a0002 | c0002 | t0003 | g0137 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18947 | hp2 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18954 | hp1 | a0002 | c0002 | t0003 | g0150 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18954 | hp2 | a0001 | c0001 | t0037 | g0243 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18957 | hp2 | a0002 | c0002 | t0003 | g0140 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18962 | hp2 | a0001 | c0001 | t0029 | g0103 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18978 | hp2 | a0001 | c0001 | t0006 | g0233 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18984 | hp2 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18987 | hp1 | a0002 | c0002 | t0003 | g0167 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18988 | hp2 | a0002 | c0002 | t0003 | g0161 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18992 | hp2 | a0001 | c0001 | t0039 | g0201 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18993 | hp2 | a0002 | c0002 | t0003 | g0157 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18994 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18995 | hp2 | a0002 | c0002 | t0003 | g0139 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18999 | hp2 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0249 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0145 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19005 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0235 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0162 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19030 | hp1 | a0001 | c0001 | t0028 | g0023 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19043 | hp1 | a0001 | c0001 | t0040 | g0293 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0033 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19057 | hp2 | a0002 | c0002 | t0003 | g0147 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19063 | hp2 | a0002 | c0002 | t0003 | g0176 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19081 | hp1 | a0002 | c0002 | t0003 | g0181 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0178 | EUR | TSI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA20805 | hp2 | a0001 | c0001 | t0013 | g0282 | EUR | TSI | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0180 | AFR | ACB | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0172 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0173 | AFR | MSL | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA20300 | hp1 | a0002 | c0002 | t0004 | g0130 | AFR | USA | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0090 | AFR | USA | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA21309 | hp1 | a0002 | c0002 | t0004 | g0113 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0184 | AFR | LWK | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0083 | REF | REF | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | TMEM87B_chr2_112050269_112124314 | TMEM87B | chr2 | 112050269 | 112124314 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112055613 | G | C | 1 | a0003 | 6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
missense_variant | MODERATE | c.22G>C | p.Val8Leu | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 345/5162 | 22/1668 | 8/555 | chr2 | 112055613 | |||
| chr2:112074958 | CAAT | C | 1 | a0002 | 77 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(74): Show |
disruptive_inframe_deletion&splice_region_variant | MODERATE | c.498_500delAAT | p.Met167del | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/19 | 821/5162 | 498/1668 | 166/555 | chr2 | 112074958 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112055717 | G | C | 1 | a0001c0004 | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.126G>C | p.Ala42Ala | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 449/5162 | 126/1668 | 42/555 | chr2 | 112055717 | |||
| chr2:112060006 | T | C | 1 | a0001c0005 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.195T>C | p.Thr65Thr | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/19 | 518/5162 | 195/1668 | 65/555 | chr2 | 112060006 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112055279 | C | G | 8 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0019 others(5): Show |
56 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-313C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 313 | chr2 | 112055279 | ||||||
| chr2:112055305 | C | T | 3 | a0001c0001t0013 a0002c0002t0012 a0002c0002t0041 |
8 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-287C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 287 | chr2 | 112055305 | ||||||
| chr2:112055307 | C | T | 2 | a0001c0001t0040 a0002c0002t0018 |
3 | HG01257.hp1 HG01258.hp2 NA19043.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-285C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | chr2 | 112055307 | |||||||
| chr2:112055428 | G | A | 2 | a0003c0003t0009 a0003c0003t0016 |
6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-164G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 164 | chr2 | 112055428 | ||||||
| chr2:112055489 | G | C | 12 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(9): Show |
65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
5_prime_UTR_variant | MODIFIER | c.-103G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 103 | chr2 | 112055489 | ||||||
| chr2:112055586 | G | A | 13 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0015 others(10): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(66): Show |
5_prime_UTR_variant | MODIFIER | c.-6G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/19 | 6 | chr2 | 112055586 | ||||||
| chr2:112116153 | G | A | 1 | a0001c0001t0021 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 10 | chr2 | 112116153 | ||||||
| chr2:112116289 | G | C | 1 | a0001c0001t0022 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 146 | chr2 | 112116289 | ||||||
| chr2:112116307 | T | A | 1 | a0001c0001t0023 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*164T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 164 | chr2 | 112116307 | ||||||
| chr2:112116308 | A | T | 1 | a0001c0001t0023 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 165 | chr2 | 112116308 | ||||||
| chr2:112116311 | G | C | 2 | a0001c0001t0017 a0001c0004t0010 |
6 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*168G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 168 | chr2 | 112116311 | ||||||
| chr2:112116313 | T | C | 2 | a0001c0001t0013 a0001c0001t0024 |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*170T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 170 | chr2 | 112116313 | ||||||
| chr2:112116514 | T | C | 1 | a0001c0001t0025 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 371 | chr2 | 112116514 | ||||||
| chr2:112116565 | C | T | 1 | a0001c0001t0011 | 4 | HG02922.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*422C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 422 | chr2 | 112116565 | ||||||
| chr2:112116594 | G | T | 2 | a0001c0001t0005 a0003c0003t0009 |
19 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*451G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 451 | chr2 | 112116594 | ||||||
| chr2:112116676 | A | G | 1 | a0001c0001t0006 | 6 | HG02027.hp2 NA18978.hp2 NA18992.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*533A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 533 | chr2 | 112116676 | ||||||
| chr2:112116879 | G | A | 2 | a0001c0001t0017 a0001c0004t0010 |
6 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*736G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 736 | chr2 | 112116879 | ||||||
| chr2:112116910 | G | A | 3 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0024 |
9 | HG00323.hp2 HG01243.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*767G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 767 | chr2 | 112116910 | ||||||
| chr2:112117007 | T | C | 3 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0042 |
3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*864T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 864 | chr2 | 112117007 | ||||||
| chr2:112117366 | AT | A | 1 | a0002c0002t0014 | 3 | HG01074.hp2 HG01081.hp1 HG01099.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1225delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1225 | INFO_REALIGN_3_PRIME | chr2 | 112117366 | |||||
| chr2:112117462 | A | G | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*1319A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1319 | chr2 | 112117462 | ||||||
| chr2:112117514 | A | T | 1 | a0002c0002t0043 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1371A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1371 | chr2 | 112117514 | ||||||
| chr2:112117662 | GA | G | 2 | a0001c0001t0039 a0002c0002t0008 |
6 | HG01109.hp1 HG01255.hp1 HG01515.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1530delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1530 | INFO_REALIGN_3_PRIME | chr2 | 112117662 | |||||
| chr2:112117697 | A | G | 1 | a0001c0001t0027 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1554A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1554 | chr2 | 112117697 | ||||||
| chr2:112117722 | G | A | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1579G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1579 | chr2 | 112117722 | ||||||
| chr2:112117967 | T | C | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1824T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1824 | chr2 | 112117967 | ||||||
| chr2:112118021 | G | A | 1 | a0002c0002t0018 | 2 | HG01257.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1878G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1878 | chr2 | 112118021 | ||||||
| chr2:112118037 | C | CT | 8 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0013 others(5): Show |
31 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1894_*1895insT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1895 | chr2 | 112118037 | ||||||
| chr2:112118141 | G | T | 1 | a0001c0001t0038 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1998G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 1998 | chr2 | 112118141 | ||||||
| chr2:112118149 | T | C | 1 | a0001c0001t0029 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2006T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2006 | chr2 | 112118149 | ||||||
| chr2:112118231 | C | T | 1 | a0001c0001t0031 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2088 | chr2 | 112118231 | ||||||
| chr2:112118233 | T | C | 1 | a0001c0001t0032 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2090T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2090 | chr2 | 112118233 | ||||||
| chr2:112118379 | C | G | 2 | a0001c0001t0017 a0001c0004t0010 |
6 | HG02451.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2236C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2236 | chr2 | 112118379 | ||||||
| chr2:112118462 | T | C | 4 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0033 others(1): Show |
23 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2319T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2319 | chr2 | 112118462 | ||||||
| chr2:112118677 | G | T | 1 | a0001c0001t0025 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2534G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2534 | chr2 | 112118677 | ||||||
| chr2:112118734 | T | G | 1 | a0001c0001t0034 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2591T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2591 | chr2 | 112118734 | ||||||
| chr2:112118798 | T | G | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2655T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2655 | chr2 | 112118798 | ||||||
| chr2:112118893 | C | A | 1 | a0001c0001t0036 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2750C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2750 | chr2 | 112118893 | ||||||
| chr2:112119001 | T | G | 1 | a0001c0001t0033 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2858T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2858 | chr2 | 112119001 | ||||||
| chr2:112119037 | T | C | 1 | a0002c0002t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2894 | chr2 | 112119037 | ||||||
| chr2:112119045 | C | G | 1 | a0001c0001t0030 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2902C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 2902 | chr2 | 112119045 | ||||||
| chr2:112119204 | G | A | 1 | a0001c0001t0037 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3061G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 3061 | chr2 | 112119204 | ||||||
| chr2:112119212 | G | T | 1 | a0001c0001t0027 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 19/19 | 3069 | chr2 | 112119212 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112055814 | C | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(226): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.165+58C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112055814 | |||||||
| chr2:112055938 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.165+182C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112055938 | |||||||
| chr2:112056107 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.165+351G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056107 | |||||||
| chr2:112056195 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.165+439A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056195 | |||||||
| chr2:112056202 | TAGAA | T | 5 | a0003c0003t0009g0013 a0003c0003t0009g0298 a0003c0003t0009g0301 others(2): Show |
6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+449_165+452del others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112056202 | ||||||
| chr2:112056206 | A | C | 1 | a0001c0001t0005g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+450A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056206 | |||||||
| chr2:112056223 | C | A | 5 | a0003c0003t0009g0013 a0003c0003t0009g0298 a0003c0003t0009g0301 others(2): Show |
6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+467C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056223 | |||||||
| chr2:112056315 | T | C | 53 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(50): Show |
55 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.165+559T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056315 | |||||||
| chr2:112056351 | A | T | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.165+595A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056351 | |||||||
| chr2:112056356 | G | A | 1 | a0001c0001t0019g0133 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.165+600G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056356 | |||||||
| chr2:112056468 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(249): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.165+712T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056468 | |||||||
| chr2:112056749 | G | A | 52 | a0001c0001t0003g0153 a0001c0001t0015g0170 a0001c0001t0015g0173 others(49): Show |
55 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.165+993G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056749 | |||||||
| chr2:112056895 | T | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG02572.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+1139T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112056895 | |||||||
| chr2:112057044 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(100): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.165+1288T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057044 | |||||||
| chr2:112057074 | G | A | 8 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(5): Show |
8 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+1318G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057074 | |||||||
| chr2:112057144 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | NA18951.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.165+1388G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057144 | |||||||
| chr2:112057314 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.165+1558C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057314 | |||||||
| chr2:112057315 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.165+1559C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057315 | |||||||
| chr2:112057344 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.165+1588T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057344 | |||||||
| chr2:112057425 | G | A | 54 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(51): Show |
56 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.165+1669G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057425 | |||||||
| chr2:112057496 | T | C | 1 | a0001c0001t0002g0285 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.165+1740T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057496 | |||||||
| chr2:112057713 | C | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(226): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.165+1957C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057713 | |||||||
| chr2:112057827 | C | CT | 44 | a0001c0001t0001g0127 a0001c0001t0001g0276 a0001c0001t0002g0004 others(41): Show |
45 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.165+2088dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112057827 | ||||||
| chr2:112057827 | CT | C | 69 | a0001c0001t0002g0182 a0001c0001t0003g0153 a0001c0001t0013g0282 others(66): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.165+2088delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112057827 | ||||||
| chr2:112057857 | C | T | 3 | a0001c0001t0040g0293 a0002c0002t0018g0291 a0002c0002t0018g0292 |
3 | HG01257.hp1 HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.165+2101C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057857 | |||||||
| chr2:112057893 | T | G | 2 | a0002c0002t0018g0291 a0002c0002t0018g0292 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.166-2084T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057893 | |||||||
| chr2:112057908 | A | G | 8 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(5): Show |
8 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-2069A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057908 | |||||||
| chr2:112057920 | C | T | 1 | a0001c0001t0013g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-2057C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057920 | |||||||
| chr2:112057928 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(226): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.166-2049G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057928 | |||||||
| chr2:112057985 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.166-1992G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112057985 | |||||||
| chr2:112058103 | G | A | 3 | a0001c0001t0040g0293 a0002c0002t0018g0291 a0002c0002t0018g0292 |
3 | HG01257.hp1 HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.166-1874G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058103 | |||||||
| chr2:112058106 | C | T | 1 | a0001c0001t0002g0036 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.166-1871C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058106 | |||||||
| chr2:112058122 | C | T | 2 | a0002c0002t0004g0032 a0002c0002t0004g0033 |
2 | HG01175.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.166-1855C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058122 | |||||||
| chr2:112058131 | T | G | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1846T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058131 | |||||||
| chr2:112058299 | G | C | 11 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0005g0087 others(8): Show |
12 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1678G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058299 | |||||||
| chr2:112058389 | T | A | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1588T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058389 | |||||||
| chr2:112058445 | T | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0024g0019 |
3 | HG02723.hp2 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.166-1532T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058445 | |||||||
| chr2:112058470 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(226): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.166-1507T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058470 | |||||||
| chr2:112058548 | T | TAA | 119 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(116): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.166-1427_166-1426d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112058548 | ||||||
| chr2:112058557 | A | T | 5 | a0003c0003t0009g0013 a0003c0003t0009g0298 a0003c0003t0009g0301 others(2): Show |
6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-1420A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058557 | |||||||
| chr2:112058659 | G | T | 65 | a0001c0001t0003g0153 a0001c0001t0013g0282 a0001c0001t0013g0283 others(62): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.166-1318G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058659 | |||||||
| chr2:112058671 | A | G | 1 | a0001c0001t0013g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-1306A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058671 | |||||||
| chr2:112058692 | T | A | 11 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0005g0087 others(8): Show |
12 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1285T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058692 | |||||||
| chr2:112058720 | C | G | 11 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0005g0087 others(8): Show |
12 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1257C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058720 | |||||||
| chr2:112058771 | A | G | 52 | a0001c0001t0003g0153 a0001c0001t0015g0170 a0001c0001t0015g0173 others(49): Show |
55 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.166-1206A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058771 | |||||||
| chr2:112058788 | G | A | 7 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0002g0039 others(4): Show |
7 | HG01361.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1189G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112058788 | |||||||
| chr2:112059157 | G | T | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.166-820G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059157 | |||||||
| chr2:112059311 | A | G | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.166-666A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059311 | |||||||
| chr2:112059328 | G | T | 2 | a0002c0002t0018g0291 a0002c0002t0018g0292 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.166-649G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059328 | |||||||
| chr2:112059487 | G | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(13): Show |
16 | HG01175.hp1 HG02280.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.166-490G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059487 | |||||||
| chr2:112059562 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.166-415C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059562 | |||||||
| chr2:112059649 | C | T | 12 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(9): Show |
12 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-328C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059649 | |||||||
| chr2:112059881 | A | T | 53 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(50): Show |
55 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.166-96A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | chr2 | 112059881 | |||||||
| chr2:112059928 | CA | C | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-41delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr2 | 112059928 | ||||||
| chr2:112060152 | C | A | 21 | a0001c0001t0002g0004 a0001c0001t0002g0086 a0001c0001t0002g0094 others(18): Show |
22 | HG01257.hp2 HG01516.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.226+115C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060152 | |||||||
| chr2:112060251 | A | G | 12 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(9): Show |
12 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.226+214A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060251 | |||||||
| chr2:112060262 | T | C | 2 | a0002c0002t0018g0291 a0002c0002t0018g0292 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.226+225T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060262 | |||||||
| chr2:112060285 | C | G | 122 | a0001c0001t0001g0127 a0001c0001t0001g0272 a0001c0001t0001g0273 others(119): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.226+248C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060285 | |||||||
| chr2:112060339 | ACT | A | 69 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(66): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.226+305_226+306del others(2): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr2 | 112060339 | ||||||
| chr2:112060381 | A | C | 41 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(38): Show |
42 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.226+344A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060381 | |||||||
| chr2:112060408 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG02572.hp1 HG02970.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+371C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060408 | |||||||
| chr2:112060434 | A | G | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.226+397A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060434 | |||||||
| chr2:112060816 | C | T | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.226+779C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060816 | |||||||
| chr2:112060931 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.226+894A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060931 | |||||||
| chr2:112060996 | A | C | 1 | a0001c0001t0002g0112 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.226+959A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112060996 | |||||||
| chr2:112061027 | C | T | 41 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(38): Show |
42 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.226+990C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061027 | |||||||
| chr2:112061054 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.226+1017G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061054 | |||||||
| chr2:112061159 | G | C | 2 | a0002c0002t0003g0134 a0002c0002t0003g0135 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.226+1122G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061159 | |||||||
| chr2:112061439 | G | A | 52 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(49): Show |
54 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.226+1402G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061439 | |||||||
| chr2:112061778 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.226+1741G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061778 | |||||||
| chr2:112061896 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.226+1859A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061896 | |||||||
| chr2:112061925 | G | C | 1 | a0002c0002t0003g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.226+1888G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112061925 | |||||||
| chr2:112062024 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
107 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.226+1987A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062024 | |||||||
| chr2:112062049 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.226+2012C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062049 | |||||||
| chr2:112062284 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.227-1878C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062284 | |||||||
| chr2:112062426 | A | G | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.227-1736A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062426 | |||||||
| chr2:112062532 | G | A | 55 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(52): Show |
58 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.227-1630G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062532 | |||||||
| chr2:112062854 | C | G | 1 | a0002c0002t0003g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.227-1308C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062854 | |||||||
| chr2:112062885 | T | C | 122 | a0001c0001t0001g0127 a0001c0001t0001g0272 a0001c0001t0001g0273 others(119): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.227-1277T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062885 | |||||||
| chr2:112062961 | C | G | 3 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0025g0111 |
3 | HG01993.hp1 HG02129.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.227-1201C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112062961 | |||||||
| chr2:112063057 | G | A | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.227-1105G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063057 | |||||||
| chr2:112063063 | A | G | 3 | a0001c0001t0005g0131 a0002c0002t0004g0130 a0002c0002t0004g0132 |
3 | HG02055.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.227-1099A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063063 | |||||||
| chr2:112063287 | G | T | 18 | a0001c0001t0001g0127 a0001c0001t0002g0123 a0001c0001t0004g0088 others(15): Show |
19 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.227-875G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063287 | |||||||
| chr2:112063288 | C | T | 18 | a0001c0001t0001g0127 a0001c0001t0002g0123 a0001c0001t0004g0088 others(15): Show |
19 | HG01070.hp2 HG01243.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.227-874C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063288 | |||||||
| chr2:112063411 | T | A | 1 | a0001c0005t0020g0290 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.227-751T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063411 | |||||||
| chr2:112063535 | C | T | 5 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0007g0090 others(2): Show |
5 | HG01243.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-627C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063535 | |||||||
| chr2:112063649 | A | G | 70 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(67): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.227-513A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063649 | |||||||
| chr2:112063710 | A | G | 1 | a0002c0002t0004g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.227-452A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063710 | |||||||
| chr2:112063769 | C | G | 9 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(6): Show |
9 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.227-393C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112063769 | |||||||
| chr2:112064020 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.227-142G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112064020 | |||||||
| chr2:112064044 | A | T | 1 | a0001c0001t0002g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.227-118A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 2/18 | chr2 | 112064044 | |||||||
| chr2:112064303 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(102): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.318+50A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064303 | |||||||
| chr2:112064343 | A | G | 1 | a0002c0002t0003g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.318+90A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064343 | |||||||
| chr2:112064390 | T | C | 1 | a0001c0001t0011g0184 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.318+137T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064390 | |||||||
| chr2:112064398 | A | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0264 a0001c0001t0001g0265 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.318+145A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064398 | |||||||
| chr2:112064410 | T | C | 1 | a0002c0002t0004g0294 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.318+157T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064410 | |||||||
| chr2:112064507 | A | G | 122 | a0001c0001t0001g0127 a0001c0001t0001g0272 a0001c0001t0001g0273 others(119): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.318+254A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064507 | |||||||
| chr2:112064596 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.318+343A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064596 | |||||||
| chr2:112064626 | G | A | 1 | a0001c0005t0020g0290 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.318+373G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064626 | |||||||
| chr2:112064727 | C | T | 70 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(67): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.318+474C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064727 | |||||||
| chr2:112064921 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.318+668T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064921 | |||||||
| chr2:112064936 | A | G | 1 | a0001c0005t0020g0290 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.318+683A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112064936 | |||||||
| chr2:112065022 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(11): Show |
17 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.318+769G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065022 | |||||||
| chr2:112065066 | C | T | 52 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(49): Show |
54 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.318+813C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065066 | |||||||
| chr2:112065254 | A | C | 1 | a0001c0001t0001g0262 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.318+1001A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065254 | |||||||
| chr2:112065304 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.318+1051T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065304 | |||||||
| chr2:112065357 | A | G | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1104A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065357 | |||||||
| chr2:112065399 | G | T | 24 | a0001c0001t0001g0127 a0001c0001t0002g0123 a0001c0001t0004g0088 others(21): Show |
26 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+1146G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065399 | |||||||
| chr2:112065463 | A | C | 24 | a0001c0001t0001g0127 a0001c0001t0002g0123 a0001c0001t0004g0088 others(21): Show |
26 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+1210A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065463 | |||||||
| chr2:112065537 | C | T | 36 | a0001c0001t0002g0004 a0001c0001t0002g0086 a0001c0001t0002g0094 others(33): Show |
37 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.318+1284C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065537 | |||||||
| chr2:112065551 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.318+1298C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065551 | |||||||
| chr2:112065576 | T | G | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1323T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065576 | |||||||
| chr2:112065643 | C | CA | 9 | a0001c0001t0001g0191 a0001c0001t0002g0046 a0001c0001t0002g0047 others(6): Show |
9 | HG00438.hp1 HG01258.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-1270dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr2 | 112065643 | ||||||
| chr2:112065643 | C | CAA | 9 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(6): Show |
9 | HG00323.hp2 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.319-1271_319-1270d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr2 | 112065643 | ||||||
| chr2:112065643 | CA | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(90): Show |
96 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.319-1270delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr2 | 112065643 | ||||||
| chr2:112065664 | A | G | 29 | a0001c0001t0001g0010 a0001c0001t0001g0183 a0001c0001t0001g0232 others(26): Show |
30 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.319-1272A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065664 | |||||||
| chr2:112065715 | C | T | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.319-1221C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065715 | |||||||
| chr2:112065727 | A | G | 1 | a0002c0002t0004g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.319-1209A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065727 | |||||||
| chr2:112065743 | C | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.319-1193C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112065743 | |||||||
| chr2:112066048 | T | C | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-888T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066048 | |||||||
| chr2:112066249 | A | G | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.319-687A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066249 | |||||||
| chr2:112066413 | T | A | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319-523T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066413 | |||||||
| chr2:112066499 | G | T | 2 | a0001c0001t0013g0282 a0001c0001t0013g0283 |
2 | HG00323.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.319-437G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066499 | |||||||
| chr2:112066834 | A | G | 1 | a0002c0002t0004g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.319-102A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 3/18 | chr2 | 112066834 | |||||||
| chr2:112067324 | G | A | 52 | a0001c0001t0002g0004 a0001c0001t0002g0086 a0001c0001t0002g0094 others(49): Show |
53 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.450+257G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067324 | |||||||
| chr2:112067363 | C | T | 76 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(73): Show |
79 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.450+296C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067363 | |||||||
| chr2:112067742 | C | T | 1 | a0002c0002t0003g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.450+675C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067742 | |||||||
| chr2:112067939 | C | T | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+872C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067939 | |||||||
| chr2:112067969 | T | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG03688.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.450+902T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112067969 | |||||||
| chr2:112068138 | C | T | 37 | a0001c0001t0002g0004 a0001c0001t0002g0086 a0001c0001t0002g0094 others(34): Show |
38 | HG01257.hp2 HG01516.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.450+1071C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068138 | |||||||
| chr2:112068170 | C | T | 72 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(69): Show |
75 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+1103C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068170 | |||||||
| chr2:112068210 | G | A | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.450+1143G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068210 | |||||||
| chr2:112068501 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(145): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.450+1434G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068501 | |||||||
| chr2:112068564 | C | T | 1 | a0002c0002t0003g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.450+1497C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068564 | |||||||
| chr2:112068661 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1594G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068661 | |||||||
| chr2:112068663 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.450+1596C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068663 | |||||||
| chr2:112068664 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.450+1597G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068664 | |||||||
| chr2:112068678 | T | C | 1 | a0001c0001t0007g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.450+1611T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068678 | |||||||
| chr2:112068698 | C | T | 1 | a0001c0001t0005g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.450+1631C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068698 | |||||||
| chr2:112068898 | G | A | 20 | a0001c0001t0001g0127 a0001c0001t0002g0123 a0001c0001t0005g0011 others(17): Show |
22 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.450+1831G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068898 | |||||||
| chr2:112068914 | C | T | 5 | a0003c0003t0009g0013 a0003c0003t0009g0298 a0003c0003t0009g0301 others(2): Show |
6 | HG01070.hp2 HG01346.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+1847C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068914 | |||||||
| chr2:112068915 | G | A | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1848G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068915 | |||||||
| chr2:112068921 | G | A | 72 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0086 others(69): Show |
75 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+1854G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068921 | |||||||
| chr2:112068963 | C | T | 1 | a0001c0001t0026g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.450+1896C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112068963 | |||||||
| chr2:112069016 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.450+1949C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069016 | |||||||
| chr2:112069019 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.450+1952C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069019 | |||||||
| chr2:112069177 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0017g0224 a0001c0001t0017g0231 |
3 | HG02451.hp2 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.450+2110C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069177 | |||||||
| chr2:112069182 | G | C | 4 | a0002c0002t0003g0005 a0002c0002t0003g0141 a0002c0002t0003g0142 others(1): Show |
5 | HG02056.hp2 HG04115.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+2115G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069182 | |||||||
| chr2:112069198 | C | CA | 57 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0185 others(54): Show |
58 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.450+2154dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112069198 | ||||||
| chr2:112069198 | C | CAA | 44 | a0001c0001t0001g0127 a0001c0001t0002g0004 a0001c0001t0002g0094 others(41): Show |
47 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.450+2153_450+2154d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112069198 | ||||||
| chr2:112069198 | C | CAAA | 24 | a0001c0001t0002g0086 a0001c0001t0002g0095 a0001c0001t0002g0096 others(21): Show |
24 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.450+2152_450+2154d others(5): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112069198 | ||||||
| chr2:112069221 | A | C | 3 | a0001c0004t0010g0287 a0001c0004t0010g0288 a0001c0004t0010g0289 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.450+2154A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069221 | |||||||
| chr2:112069392 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.450+2325C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069392 | |||||||
| chr2:112069711 | C | T | 3 | a0001c0001t0040g0293 a0002c0002t0018g0291 a0002c0002t0018g0292 |
3 | HG01257.hp1 HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.450+2644C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069711 | |||||||
| chr2:112069834 | G | C | 53 | a0001c0001t0002g0004 a0001c0001t0002g0086 a0001c0001t0002g0094 others(50): Show |
54 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.450+2767G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069834 | |||||||
| chr2:112069862 | A | G | 53 | a0001c0001t0002g0004 a0001c0001t0002g0086 a0001c0001t0002g0094 others(50): Show |
54 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.450+2795A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112069862 | |||||||
| chr2:112070218 | T | G | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.450+3151T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070218 | |||||||
| chr2:112070242 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.450+3175C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070242 | |||||||
| chr2:112070401 | AGT | A | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG01433.hp1 NA18747.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.450+3335_450+3336d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070401 | |||||||
| chr2:112070722 | G | A | 2 | a0002c0002t0008g0144 a0002c0002t0008g0148 |
2 | HG01255.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.450+3655G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070722 | |||||||
| chr2:112070868 | C | G | 1 | a0002c0002t0004g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450+3801C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070868 | |||||||
| chr2:112070882 | C | T | 63 | a0001c0001t0001g0010 a0001c0001t0001g0183 a0001c0001t0001g0232 others(60): Show |
65 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.450+3815C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070882 | |||||||
| chr2:112070915 | G | A | 1 | a0001c0001t0039g0201 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.450+3848G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112070915 | |||||||
| chr2:112071046 | T | C | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3866T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071046 | |||||||
| chr2:112071047 | G | A | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3865G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071047 | |||||||
| chr2:112071058 | T | C | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3854T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071058 | |||||||
| chr2:112071201 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(181): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.451-3711T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071201 | |||||||
| chr2:112071297 | T | TC | 18 | a0001c0001t0001g0202 a0001c0001t0001g0226 a0001c0001t0001g0238 others(15): Show |
18 | HG01109.hp2 HG01192.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.451-3607dupC | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112071297 | ||||||
| chr2:112071306 | G | C | 4 | a0001c0001t0001g0246 a0001c0001t0001g0268 a0001c0001t0002g0070 others(1): Show |
4 | HG00642.hp1 HG03669.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3606G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071306 | |||||||
| chr2:112071306 | G | GC | 16 | a0001c0001t0001g0183 a0001c0001t0001g0191 a0001c0001t0001g0203 others(13): Show |
16 | HG00639.hp2 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.451-3599dupC | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112071306 | ||||||
| chr2:112071308 | C | G | 1 | a0002c0002t0001g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.451-3604C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071308 | |||||||
| chr2:112071314 | G | C | 1 | a0002c0002t0001g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.451-3598G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071314 | |||||||
| chr2:112071328 | T | G | 1 | a0001c0001t0038g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.451-3584T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071328 | |||||||
| chr2:112071462 | C | T | 1 | a0003c0003t0009g0301 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.451-3450C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071462 | |||||||
| chr2:112071524 | C | A | 1 | a0001c0001t0026g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.451-3388C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071524 | |||||||
| chr2:112071598 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(87): Show |
96 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.451-3314C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071598 | |||||||
| chr2:112071806 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0191 a0001c0001t0001g0193 others(30): Show |
35 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.451-3106C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071806 | |||||||
| chr2:112071810 | C | T | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.451-3102C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071810 | |||||||
| chr2:112071936 | T | TA | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-2975dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112071936 | ||||||
| chr2:112071941 | T | G | 1 | a0001c0001t0002g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.451-2971T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112071941 | |||||||
| chr2:112072105 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(235): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.451-2807G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072105 | |||||||
| chr2:112072332 | G | A | 5 | a0001c0001t0033g0093 a0001c0004t0010g0286 a0001c0004t0010g0287 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-2580G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072332 | |||||||
| chr2:112072396 | T | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(10): Show |
16 | HG00621.hp1 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.451-2516T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072396 | |||||||
| chr2:112072409 | C | G | 3 | a0001c0001t0026g0022 a0001c0001t0027g0296 a0001c0001t0042g0297 |
3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.451-2503C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072409 | |||||||
| chr2:112072410 | G | A | 1 | a0002c0002t0043g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.451-2502G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072410 | |||||||
| chr2:112072588 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(189): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.451-2324C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072588 | |||||||
| chr2:112072703 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.451-2209C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072703 | |||||||
| chr2:112072788 | A | G | 19 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.451-2124A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112072788 | |||||||
| chr2:112072895 | C | CT | 83 | a0001c0001t0001g0127 a0001c0001t0001g0214 a0001c0001t0001g0215 others(80): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.451-1995dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112072895 | ||||||
| chr2:112072895 | CT | C | 14 | a0001c0001t0001g0027 a0001c0001t0001g0187 a0001c0001t0001g0248 others(11): Show |
14 | HG01070.hp1 HG01167.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.451-1995delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr2 | 112072895 | ||||||
| chr2:112073097 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.451-1815G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073097 | |||||||
| chr2:112073244 | C | T | 1 | a0002c0002t0003g0176 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.451-1668C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073244 | |||||||
| chr2:112073259 | T | C | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.451-1653T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073259 | |||||||
| chr2:112073344 | C | T | 1 | a0001c0001t0007g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.451-1568C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073344 | |||||||
| chr2:112073414 | C | T | 1 | a0001c0004t0010g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.451-1498C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073414 | |||||||
| chr2:112073491 | T | C | 4 | a0001c0001t0011g0184 a0001c0001t0011g0206 a0001c0001t0011g0216 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1421T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073491 | |||||||
| chr2:112073558 | A | T | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.451-1354A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073558 | |||||||
| chr2:112073573 | A | G | 1 | a0001c0001t0028g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451-1339A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073573 | |||||||
| chr2:112073769 | G | A | 1 | a0001c0001t0007g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.451-1143G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073769 | |||||||
| chr2:112073848 | G | T | 1 | a0001c0001t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.451-1064G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112073848 | |||||||
| chr2:112074041 | T | C | 1 | a0002c0002t0008g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.451-871T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112074041 | |||||||
| chr2:112074085 | G | A | 22 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(19): Show |
24 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.451-827G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112074085 | |||||||
| chr2:112074106 | G | A | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.451-806G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 4/18 | chr2 | 112074106 | |||||||
| chr2:112075005 | A | T | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.501+43A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075005 | |||||||
| chr2:112075092 | A | G | 3 | a0001c0001t0011g0184 a0001c0001t0011g0206 a0001c0001t0011g0216 |
3 | HG02922.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.501+130A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075092 | |||||||
| chr2:112075245 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(87): Show |
96 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.501+283C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075245 | |||||||
| chr2:112075531 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.501+569C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075531 | |||||||
| chr2:112075534 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.501+572C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075534 | |||||||
| chr2:112075850 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.501+888G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075850 | |||||||
| chr2:112075940 | G | A | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.501+978G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112075940 | |||||||
| chr2:112076123 | G | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-1069G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076123 | |||||||
| chr2:112076426 | G | C | 1 | a0001c0001t0005g0087 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.502-766G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076426 | |||||||
| chr2:112076567 | T | C | 1 | a0001c0001t0031g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.502-625T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076567 | |||||||
| chr2:112076587 | A | C | 30 | a0001c0001t0001g0060 a0001c0001t0002g0046 a0001c0001t0002g0047 others(27): Show |
30 | HG00408.hp2 HG00558.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.502-605A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076587 | |||||||
| chr2:112076822 | C | T | 2 | a0002c0002t0003g0166 a0002c0002t0003g0178 |
2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.502-370C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076822 | |||||||
| chr2:112076841 | TTTGTGTG others(12): Show |
T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.502-349_502-331del others(19): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076841 | ||||||
| chr2:112076842 | T | TTG | 10 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0045 others(7): Show |
10 | HG01361.hp1 HG01928.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.502-304_502-303dup others(2): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | T | TTGTG | 27 | a0001c0001t0002g0003 a0001c0001t0002g0035 a0001c0001t0002g0039 others(24): Show |
27 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.502-306_502-303dup others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | T | TTGTGTG | 8 | a0001c0001t0001g0060 a0001c0001t0002g0004 a0001c0001t0002g0046 others(5): Show |
8 | HG01255.hp2 HG01516.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.502-308_502-303dup others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | T | TTGTGTGT others(1): Show |
5 | a0001c0001t0002g0004 a0001c0001t0002g0056 a0001c0001t0002g0059 others(2): Show |
5 | HG01257.hp2 HG01433.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-310_502-303dup others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0002g0063 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.502-316_502-303dup others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | TTGTGTG | T | 22 | a0001c0001t0002g0034 a0001c0001t0002g0241 a0001c0001t0004g0088 others(19): Show |
24 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.502-308_502-303del others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | TTGTGTGT others(1): Show |
T | 24 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): Show |
24 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.502-310_502-303del others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | TTGTGTGT others(3): Show |
T | 16 | a0001c0001t0001g0020 a0001c0001t0002g0094 a0001c0001t0002g0095 others(13): Show |
16 | HG00140.hp2 HG01928.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.502-312_502-303del others(10): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502-314_502-303del others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | TTGTGTGT others(7): Show |
T | 2 | a0001c0001t0002g0242 a0002c0002t0004g0294 |
2 | HG03017.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.502-316_502-303del others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0245 |
2 | NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.502-318_502-303del others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0001g0268 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.502-320_502-303del others(18): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076842 | TTGTGTGT others(13): Show |
T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(162): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.502-322_502-303del others(20): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112076842 | ||||||
| chr2:112076852 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.502-340G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076852 | |||||||
| chr2:112076929 | T | C | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.502-263T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112076929 | |||||||
| chr2:112077028 | A | G | 1 | a0001c0001t0034g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.502-164A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | chr2 | 112077028 | |||||||
| chr2:112077038 | C | CA | 81 | a0001c0001t0001g0195 a0001c0001t0001g0217 a0001c0001t0002g0075 others(78): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.502-136dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112077038 | ||||||
| chr2:112077038 | CA | C | 37 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
39 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.502-136delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr2 | 112077038 | ||||||
| chr2:112077299 | T | C | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+17T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077299 | |||||||
| chr2:112077562 | A | T | 1 | a0001c0001t0038g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.592+280A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077562 | |||||||
| chr2:112077563 | T | A | 22 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(19): Show |
24 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.592+281T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077563 | |||||||
| chr2:112077564 | T | A | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.592+282T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077564 | |||||||
| chr2:112077737 | G | T | 1 | a0001c0001t0028g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.592+455G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077737 | |||||||
| chr2:112077748 | T | G | 2 | a0002c0002t0004g0130 a0002c0002t0004g0132 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.592+466T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112077748 | |||||||
| chr2:112078061 | C | T | 6 | a0001c0001t0002g0056 a0001c0001t0002g0058 a0001c0001t0002g0066 others(3): Show |
6 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+779C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078061 | |||||||
| chr2:112078096 | G | A | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.592+814G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078096 | |||||||
| chr2:112078126 | G | A | 1 | a0001c0001t0002g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.592+844G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078126 | |||||||
| chr2:112078274 | G | A | 1 | a0001c0001t0005g0126 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.592+992G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078274 | |||||||
| chr2:112078285 | G | A | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.592+1003G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078285 | |||||||
| chr2:112078360 | C | T | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.592+1078C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078360 | |||||||
| chr2:112078435 | G | A | 19 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.592+1153G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078435 | |||||||
| chr2:112078533 | C | G | 6 | a0002c0002t0001g0025 a0002c0002t0012g0278 a0002c0002t0012g0279 others(3): Show |
6 | HG02451.hp1 HG02895.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+1251C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078533 | |||||||
| chr2:112078538 | C | T | 1 | a0002c0002t0003g0164 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.592+1256C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078538 | |||||||
| chr2:112078736 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.592+1454C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078736 | |||||||
| chr2:112078749 | A | G | 3 | a0001c0001t0002g0073 a0001c0001t0002g0078 a0001c0001t0002g0085 |
3 | HG00558.hp1 NA18948.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.592+1467A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112078749 | |||||||
| chr2:112079005 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.592+1723T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079005 | |||||||
| chr2:112079083 | A | G | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.592+1801A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079083 | |||||||
| chr2:112079311 | C | T | 6 | a0001c0001t0005g0031 a0001c0001t0007g0029 a0001c0001t0007g0090 others(3): Show |
6 | HG01243.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.593-1746C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079311 | |||||||
| chr2:112079384 | C | A | 5 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0015g0170 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1673C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079384 | |||||||
| chr2:112079763 | C | T | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.593-1294C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079763 | |||||||
| chr2:112079926 | C | CT | 74 | a0001c0001t0001g0195 a0001c0001t0002g0065 a0001c0001t0002g0075 others(71): Show |
77 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.593-1110dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr2 | 112079926 | ||||||
| chr2:112079926 | C | CTT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(99): Show |
108 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.593-1111_593-1110d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr2 | 112079926 | ||||||
| chr2:112079926 | CT | C | 24 | a0001c0001t0001g0127 a0001c0001t0002g0048 a0001c0001t0002g0095 others(21): Show |
26 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.593-1110delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr2 | 112079926 | ||||||
| chr2:112079962 | C | T | 19 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.593-1095C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079962 | |||||||
| chr2:112079981 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.593-1076G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112079981 | |||||||
| chr2:112080079 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(92): Show |
101 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.593-978G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080079 | |||||||
| chr2:112080149 | G | A | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.593-908G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080149 | |||||||
| chr2:112080252 | A | T | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.593-805A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080252 | |||||||
| chr2:112080452 | T | G | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.593-605T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080452 | |||||||
| chr2:112080461 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.593-596G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080461 | |||||||
| chr2:112080481 | G | C | 4 | a0001c0001t0002g0056 a0001c0001t0002g0069 a0001c0001t0002g0182 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.593-576G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080481 | |||||||
| chr2:112080626 | T | C | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.593-431T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080626 | |||||||
| chr2:112080728 | A | T | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.593-329A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080728 | |||||||
| chr2:112080771 | G | A | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.593-286G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080771 | |||||||
| chr2:112080796 | A | C | 5 | a0001c0001t0026g0022 a0001c0001t0027g0296 a0001c0001t0042g0297 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-261A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 6/18 | chr2 | 112080796 | |||||||
| chr2:112081268 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.655-67A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 7/18 | chr2 | 112081268 | |||||||
| chr2:112081710 | A | G | 5 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0194 others(2): Show |
5 | HG01175.hp2 HG01346.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+192A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081710 | |||||||
| chr2:112081888 | T | C | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.838+370T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081888 | |||||||
| chr2:112081891 | C | T | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.838+373C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081891 | |||||||
| chr2:112081892 | C | T | 3 | a0001c0001t0026g0022 a0001c0001t0027g0296 a0001c0001t0042g0297 |
3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838+374C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081892 | |||||||
| chr2:112081918 | G | A | 6 | a0001c0001t0005g0031 a0001c0001t0007g0029 a0001c0001t0007g0090 others(3): Show |
6 | HG01243.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+400G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112081918 | |||||||
| chr2:112082056 | C | T | 3 | a0001c0001t0026g0022 a0001c0001t0027g0296 a0001c0001t0042g0297 |
3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838+538C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082056 | |||||||
| chr2:112082086 | A | G | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.838+568A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082086 | |||||||
| chr2:112082088 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.838+570G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082088 | |||||||
| chr2:112082111 | T | C | 3 | a0001c0001t0026g0022 a0001c0001t0027g0296 a0001c0001t0042g0297 |
3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838+593T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082111 | |||||||
| chr2:112082112 | G | A | 6 | a0001c0001t0005g0031 a0001c0001t0007g0029 a0001c0001t0007g0090 others(3): Show |
6 | HG01243.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+594G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082112 | |||||||
| chr2:112082216 | A | G | 20 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(17): Show |
22 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.838+698A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082216 | |||||||
| chr2:112082284 | G | A | 3 | a0001c0001t0005g0131 a0001c0001t0017g0224 a0001c0001t0017g0231 |
3 | HG02055.hp2 HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.838+766G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082284 | |||||||
| chr2:112082301 | G | A | 1 | a0001c0001t0028g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.838+783G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082301 | |||||||
| chr2:112082657 | G | GGT | 6 | a0001c0001t0002g0212 a0001c0004t0010g0286 a0001c0004t0010g0287 others(3): Show |
6 | HG02165.hp1 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+1157_838+1158d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112082657 | ||||||
| chr2:112082657 | GGTGT | G | 6 | a0001c0001t0005g0031 a0001c0001t0007g0029 a0001c0001t0007g0090 others(3): Show |
6 | HG01243.hp2 HG03098.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+1155_838+1158d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112082657 | ||||||
| chr2:112082657 | GGTGTGT | G | 3 | a0001c0001t0002g0098 a0001c0001t0002g0104 a0001c0001t0002g0105 |
3 | HG01928.hp2 HG01934.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.838+1153_838+1158d others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112082657 | ||||||
| chr2:112082841 | T | C | 3 | a0001c0001t0026g0022 a0001c0001t0027g0296 a0001c0001t0042g0297 |
3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838+1323T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082841 | |||||||
| chr2:112082926 | C | T | 20 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(17): Show |
22 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.838+1408C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112082926 | |||||||
| chr2:112083102 | A | G | 1 | a0001c0001t0007g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.838+1584A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112083102 | |||||||
| chr2:112083344 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.838+1826C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112083344 | |||||||
| chr2:112083568 | G | A | 5 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(2): Show |
5 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.838+2050G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112083568 | |||||||
| chr2:112084029 | A | G | 1 | a0001c0001t0005g0087 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.839-1976A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084029 | |||||||
| chr2:112084183 | G | A | 20 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(17): Show |
22 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-1822G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084183 | |||||||
| chr2:112084225 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.839-1780G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084225 | |||||||
| chr2:112084261 | G | T | 5 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0015g0170 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-1744G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084261 | |||||||
| chr2:112084269 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.839-1736A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084269 | |||||||
| chr2:112084279 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(193): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.839-1726T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084279 | |||||||
| chr2:112084470 | T | C | 23 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(20): Show |
25 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.839-1535T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084470 | |||||||
| chr2:112084473 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.839-1532C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084473 | |||||||
| chr2:112084513 | C | T | 1 | a0002c0002t0008g0154 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.839-1492C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084513 | |||||||
| chr2:112084589 | A | AGATCTAT others(7): Show |
6 | a0001c0001t0001g0197 a0001c0001t0001g0214 a0001c0001t0001g0215 others(3): Show |
6 | HG00438.hp2 NA18939.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.839-1414_839-1401d others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112084589 | ||||||
| chr2:112084642 | A | G | 1 | a0002c0002t0004g0024 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.839-1363A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112084642 | |||||||
| chr2:112085231 | A | C | 21 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0097 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.839-774A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085231 | |||||||
| chr2:112085346 | T | A | 71 | a0002c0002t0001g0025 a0002c0002t0001g0199 a0002c0002t0001g0207 others(68): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.839-659T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085346 | |||||||
| chr2:112085667 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(169): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.839-338A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085667 | |||||||
| chr2:112085672 | A | C | 1 | a0001c0001t0001g0262 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.839-333A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085672 | |||||||
| chr2:112085768 | G | A | 1 | a0002c0002t0003g0159 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.839-237G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085768 | |||||||
| chr2:112085820 | G | T | 23 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0087 others(20): Show |
25 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.839-185G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085820 | |||||||
| chr2:112085825 | G | A | 2 | a0002c0002t0018g0291 a0002c0002t0018g0292 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.839-180G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | chr2 | 112085825 | |||||||
| chr2:112085988 | AT | A | 48 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(45): Show |
52 | HG00558.hp2 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.839-10delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr2 | 112085988 | ||||||
| chr2:112086398 | G | A | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.938+294G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112086398 | |||||||
| chr2:112086514 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(230): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.938+410T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112086514 | |||||||
| chr2:112087066 | G | A | 3 | a0001c0001t0026g0022 a0001c0001t0027g0296 a0001c0001t0042g0297 |
3 | HG02145.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.938+962G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087066 | |||||||
| chr2:112087291 | A | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.938+1187A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087291 | |||||||
| chr2:112087390 | A | G | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.938+1286A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087390 | |||||||
| chr2:112087407 | T | TC | 18 | a0001c0001t0005g0011 a0001c0001t0005g0087 a0001c0001t0005g0124 others(15): Show |
20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.938+1303_938+1304i others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087407 | |||||||
| chr2:112087416 | ACT | A | 3 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0024g0019 |
3 | HG00323.hp2 HG02723.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.938+1315_938+1316d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr2 | 112087416 | ||||||
| chr2:112087422 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.938+1318C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087422 | |||||||
| chr2:112087526 | G | A | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.938+1422G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087526 | |||||||
| chr2:112087756 | C | G | 1 | a0002c0002t0003g0167 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.938+1652C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087756 | |||||||
| chr2:112087818 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(171): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.938+1714A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112087818 | |||||||
| chr2:112088017 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.939-1608C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088017 | |||||||
| chr2:112088027 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.939-1598C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088027 | |||||||
| chr2:112088487 | A | G | 4 | a0001c0001t0001g0195 a0001c0001t0001g0202 a0001c0001t0001g0223 others(1): Show |
4 | NA18948.hp1 NA18960.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.939-1138A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088487 | |||||||
| chr2:112088674 | A | G | 1 | a0001c0001t0019g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.939-951A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088674 | |||||||
| chr2:112088783 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(172): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.939-842A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088783 | |||||||
| chr2:112088798 | G | A | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939-827G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088798 | |||||||
| chr2:112088846 | C | G | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939-779C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088846 | |||||||
| chr2:112088861 | C | T | 1 | a0001c0001t0013g0282 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.939-764C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088861 | |||||||
| chr2:112088962 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.939-663C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112088962 | |||||||
| chr2:112089416 | A | C | 18 | a0001c0001t0005g0011 a0001c0001t0005g0087 a0001c0001t0005g0124 others(15): Show |
20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.939-209A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089416 | |||||||
| chr2:112089454 | C | T | 1 | a0001c0001t0023g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.939-171C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089454 | |||||||
| chr2:112089511 | A | C | 18 | a0001c0001t0005g0011 a0001c0001t0005g0087 a0001c0001t0005g0124 others(15): Show |
20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.939-114A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089511 | |||||||
| chr2:112089577 | C | G | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.939-48C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089577 | |||||||
| chr2:112089587 | C | T | 73 | a0002c0002t0001g0025 a0002c0002t0001g0199 a0002c0002t0001g0207 others(70): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.939-38C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 9/18 | chr2 | 112089587 | |||||||
| chr2:112090020 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1032+302G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090020 | |||||||
| chr2:112090041 | T | A | 2 | a0001c0001t0001g0197 a0001c0001t0039g0201 |
2 | NA18978.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1032+323T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090041 | |||||||
| chr2:112090169 | A | G | 3 | a0002c0002t0004g0030 a0002c0002t0004g0130 a0002c0002t0004g0132 |
3 | HG03195.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1032+451A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090169 | |||||||
| chr2:112090324 | T | G | 1 | a0001c0001t0002g0075 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1032+606T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090324 | |||||||
| chr2:112090379 | A | ATTGG | 24 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0097 others(21): Show |
24 | HG00140.hp2 HG00280.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.1032+704_1032+707d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112090379 | ||||||
| chr2:112090379 | ATTGG | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(98): Show |
107 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1032+704_1032+707d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112090379 | ||||||
| chr2:112090379 | ATTGGTTG others(1): Show |
A | 5 | a0001c0001t0001g0218 a0001c0001t0001g0270 a0001c0001t0002g0212 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+700_1032+707d others(10): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112090379 | ||||||
| chr2:112090379 | ATTGGTTG others(5): Show |
A | 70 | a0001c0001t0037g0243 a0002c0002t0001g0025 a0002c0002t0001g0199 others(67): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1032+696_1032+707d others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112090379 | ||||||
| chr2:112090522 | A | G | 18 | a0001c0001t0005g0011 a0001c0001t0005g0087 a0001c0001t0005g0124 others(15): Show |
20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1032+804A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090522 | |||||||
| chr2:112090627 | A | C | 5 | a0002c0002t0001g0025 a0002c0002t0012g0278 a0002c0002t0012g0280 others(2): Show |
5 | HG02451.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1032+909A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090627 | |||||||
| chr2:112090821 | A | G | 1 | a0001c0001t0028g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1033-891A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090821 | |||||||
| chr2:112090903 | G | A | 18 | a0001c0001t0005g0011 a0001c0001t0005g0087 a0001c0001t0005g0124 others(15): Show |
20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1033-809G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112090903 | |||||||
| chr2:112091196 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1033-516C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091196 | |||||||
| chr2:112091240 | CA | C | 7 | a0001c0001t0001g0027 a0001c0001t0002g0074 a0001c0001t0005g0261 others(4): Show |
7 | HG00639.hp1 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1033-456delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr2 | 112091240 | ||||||
| chr2:112091256 | A | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0211 |
2 | NA18994.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1033-456A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091256 | |||||||
| chr2:112091328 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0218 a0001c0001t0001g0221 |
3 | NA18747.hp2 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1033-384C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091328 | |||||||
| chr2:112091516 | AT | A | 18 | a0001c0001t0005g0011 a0001c0001t0005g0087 a0001c0001t0005g0124 others(15): Show |
20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1033-195delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091516 | |||||||
| chr2:112091656 | C | T | 3 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0015g0170 |
3 | HG02615.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1033-56C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 10/18 | chr2 | 112091656 | |||||||
| chr2:112092310 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1104+527A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112092310 | |||||||
| chr2:112092429 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1104+646C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112092429 | |||||||
| chr2:112092734 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1104+951T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112092734 | |||||||
| chr2:112093004 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(99): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1104+1221T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093004 | |||||||
| chr2:112093056 | C | T | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1104+1273C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093056 | |||||||
| chr2:112093066 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1104+1283T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093066 | |||||||
| chr2:112093202 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1104+1419G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093202 | |||||||
| chr2:112093319 | G | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1104+1536G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093319 | |||||||
| chr2:112093354 | T | G | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1104+1571T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093354 | |||||||
| chr2:112093430 | A | T | 1 | a0002c0002t0004g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1104+1647A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093430 | |||||||
| chr2:112093488 | T | C | 1 | a0001c0001t0015g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1104+1705T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093488 | |||||||
| chr2:112093847 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1104+2064A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093847 | |||||||
| chr2:112093947 | G | A | 1 | a0002c0002t0004g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1104+2164G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093947 | |||||||
| chr2:112093987 | T | C | 1 | a0002c0002t0012g0280 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1104+2204T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112093987 | |||||||
| chr2:112094112 | A | G | 1 | a0002c0002t0004g0121 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1104+2329A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094112 | |||||||
| chr2:112094161 | C | CT | 8 | a0001c0001t0001g0225 a0001c0001t0001g0263 a0001c0001t0002g0050 others(5): Show |
8 | HG00621.hp1 HG01074.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1104+2397dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112094161 | ||||||
| chr2:112094194 | G | A | 2 | a0002c0002t0004g0130 a0002c0002t0004g0132 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1104+2411G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094194 | |||||||
| chr2:112094246 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1104+2463C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094246 | |||||||
| chr2:112094380 | C | G | 1 | a0002c0002t0003g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1104+2597C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094380 | |||||||
| chr2:112094409 | C | T | 3 | a0002c0002t0004g0032 a0002c0002t0004g0033 a0002c0002t0004g0121 |
3 | HG01175.hp1 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1104+2626C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094409 | |||||||
| chr2:112094953 | G | A | 2 | a0001c0001t0002g0123 a0001c0001t0002g0229 |
2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1105-2091G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112094953 | |||||||
| chr2:112095051 | A | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1105-1993A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095051 | |||||||
| chr2:112095140 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1105-1904C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095140 | |||||||
| chr2:112095141 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(95): Show |
104 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1105-1903G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095141 | |||||||
| chr2:112095161 | CTTTCTTT others(10): Show |
C | 1 | a0001c0001t0002g0047 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1105-1879_1105-186 others(21): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095161 | ||||||
| chr2:112095165 | C | CT | 7 | a0001c0001t0002g0071 a0001c0001t0002g0075 a0001c0001t0002g0076 others(4): Show |
7 | HG00140.hp1 HG01081.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-1832dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(2): Show |
7 | a0002c0002t0003g0134 a0002c0002t0003g0135 a0002c0002t0003g0138 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-1840_1105-183 others(13): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(3): Show |
2 | a0002c0002t0003g0150 a0002c0002t0003g0164 |
2 | HG03491.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1105-1841_1105-183 others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(5): Show |
3 | a0001c0005t0020g0290 a0002c0002t0001g0199 a0002c0002t0003g0160 |
3 | HG01109.hp2 HG03654.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1105-1843_1105-183 others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(6): Show |
2 | a0002c0002t0001g0222 a0002c0002t0008g0007 |
2 | HG02698.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1105-1844_1105-183 others(17): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(7): Show |
1 | a0002c0002t0008g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1105-1845_1105-183 others(18): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(8): Show |
1 | a0002c0002t0003g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1105-1846_1105-183 others(19): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(9): Show |
1 | a0002c0002t0003g0155 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1105-1847_1105-183 others(20): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(12): Show |
3 | a0002c0002t0003g0159 a0002c0002t0014g0151 a0002c0002t0014g0152 |
3 | HG00099.hp2 HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1105-1850_1105-183 others(23): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | C | CTTTTTTT others(13): Show |
1 | a0002c0002t0014g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1105-1851_1105-183 others(24): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTT | C | 6 | a0001c0001t0002g0084 a0001c0001t0007g0029 a0001c0001t0007g0091 others(3): Show |
6 | HG01109.hp1 HG02922.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-1834_1105-183 others(7): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTT | C | 15 | a0001c0001t0001g0060 a0001c0001t0002g0049 a0001c0001t0002g0051 others(12): Show |
15 | HG01175.hp2 HG01192.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1105-1835_1105-183 others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTT | C | 14 | a0001c0001t0002g0034 a0001c0001t0002g0046 a0001c0001t0002g0050 others(11): Show |
14 | HG00099.hp1 HG00408.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1105-1836_1105-183 others(9): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT | C | 7 | a0001c0001t0002g0045 a0001c0001t0002g0106 a0001c0001t0002g0253 others(4): Show |
7 | HG00140.hp2 HG01257.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-1838_1105-183 others(11): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0002g0095 a0001c0001t0002g0097 a0001c0001t0002g0099 others(7): Show |
10 | HG02129.hp2 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1105-1839_1105-183 others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0015g0173 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-1841_1105-183 others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0003g0005 a0002c0002t0003g0143 |
2 | HG04115.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1105-1842_1105-183 others(15): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(5): Show |
C | 4 | a0002c0002t0003g0005 a0002c0002t0003g0141 a0002c0002t0003g0142 others(1): Show |
4 | HG02056.hp2 HG03195.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-1843_1105-183 others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0002g0101 a0002c0002t0004g0118 a0002c0002t0004g0130 others(1): Show |
4 | HG01258.hp1 HG02135.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-1844_1105-183 others(17): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0002g0102 a0002c0002t0001g0025 a0002c0002t0004g0117 |
3 | HG01256.hp2 HG02965.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1105-1845_1105-183 others(18): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(8): Show |
C | 5 | a0002c0002t0004g0115 a0002c0002t0004g0116 a0002c0002t0004g0120 others(2): Show |
5 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105-1846_1105-183 others(19): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(9): Show |
C | 9 | a0001c0001t0005g0087 a0001c0001t0005g0129 a0001c0001t0005g0257 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1105-1847_1105-183 others(20): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(10): Show |
C | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0124 others(16): Show |
20 | HG00639.hp1 HG01346.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1105-1848_1105-183 others(21): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1105-1849_1105-183 others(22): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1105-1850_1105-183 others(23): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(13): Show |
C | 1 | a0002c0002t0003g0172 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1105-1851_1105-183 others(24): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(14): Show |
C | 6 | a0001c0001t0026g0022 a0001c0001t0042g0297 a0002c0002t0001g0207 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-1852_1105-183 others(25): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0040g0293 a0002c0002t0004g0024 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1105-1853_1105-183 others(26): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(16): Show |
C | 10 | a0001c0001t0001g0190 a0001c0001t0001g0225 a0001c0001t0001g0238 others(7): Show |
10 | HG00438.hp1 HG00438.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1105-1854_1105-183 others(27): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(17): Show |
C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(85): Show |
94 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1105-1855_1105-183 others(28): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(18): Show |
C | 7 | a0001c0001t0001g0185 a0001c0001t0001g0221 a0001c0001t0001g0228 others(4): Show |
7 | HG00323.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105-1856_1105-183 others(29): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(19): Show |
C | 6 | a0001c0001t0002g0036 a0001c0001t0002g0064 a0001c0001t0002g0065 others(3): Show |
6 | HG02145.hp2 NA18942.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1105-1857_1105-183 others(30): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(20): Show |
C | 1 | a0001c0001t0002g0035 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1105-1858_1105-183 others(31): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(21): Show |
C | 1 | a0002c0002t0003g0006 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1105-1859_1105-183 others(32): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(25): Show |
C | 1 | a0001c0001t0007g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1105-1863_1105-183 others(36): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095165 | CTTTTTTT others(28): Show |
C | 1 | a0002c0002t0008g0148 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1105-1866_1105-183 others(39): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095165 | ||||||
| chr2:112095195 | T | C | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1105-1849T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095195 | |||||||
| chr2:112095208 | TTTTTG | T | 7 | a0001c0001t0002g0039 a0001c0001t0002g0044 a0001c0001t0002g0056 others(4): Show |
7 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105-1835_1105-183 others(9): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095208 | |||||||
| chr2:112095213 | G | T | 1 | a0001c0001t0002g0254 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1105-1831G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095213 | |||||||
| chr2:112095281 | C | T | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1105-1763C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095281 | |||||||
| chr2:112095464 | C | A | 1 | a0001c0001t0034g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1105-1580C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095464 | |||||||
| chr2:112095508 | A | AT | 6 | a0001c0001t0001g0060 a0001c0001t0002g0046 a0001c0001t0002g0048 others(3): Show |
6 | HG02132.hp2 HG02165.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105-1527dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr2 | 112095508 | ||||||
| chr2:112095642 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1105-1402T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095642 | |||||||
| chr2:112095725 | T | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(171): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1105-1319T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095725 | |||||||
| chr2:112095762 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1105-1282A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095762 | |||||||
| chr2:112095840 | G | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1105-1204G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112095840 | |||||||
| chr2:112096037 | G | C | 1 | a0001c0001t0001g0218 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1105-1007G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096037 | |||||||
| chr2:112096068 | C | T | 2 | a0002c0002t0001g0199 a0002c0002t0001g0222 |
2 | NA18940.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1105-976C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096068 | |||||||
| chr2:112096118 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0236 others(9): Show |
13 | HG00558.hp2 HG01978.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1105-926A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096118 | |||||||
| chr2:112096146 | G | A | 71 | a0002c0002t0001g0025 a0002c0002t0001g0199 a0002c0002t0001g0207 others(68): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1105-898G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096146 | |||||||
| chr2:112096166 | G | A | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1105-878G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096166 | |||||||
| chr2:112096336 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(193): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1105-708G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096336 | |||||||
| chr2:112096401 | A | G | 4 | a0001c0001t0011g0184 a0001c0001t0011g0206 a0001c0001t0011g0216 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1105-643A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096401 | |||||||
| chr2:112096477 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(193): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1105-567G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096477 | |||||||
| chr2:112096490 | G | A | 1 | a0002c0002t0004g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1105-554G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096490 | |||||||
| chr2:112096507 | A | G | 1 | a0002c0002t0004g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1105-537A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096507 | |||||||
| chr2:112096758 | G | A | 1 | a0001c0001t0028g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1105-286G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096758 | |||||||
| chr2:112096819 | G | A | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1105-225G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112096819 | |||||||
| chr2:112097007 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(93): Show |
102 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1105-37A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 11/18 | chr2 | 112097007 | |||||||
| chr2:112097354 | C | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1272+63C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097354 | |||||||
| chr2:112097356 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1272+65A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097356 | |||||||
| chr2:112097390 | A | T | 1 | a0001c0001t0001g0236 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1272+99A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097390 | |||||||
| chr2:112097554 | G | A | 1 | a0002c0002t0001g0025 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1272+263G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097554 | |||||||
| chr2:112097582 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0185 |
3 | NA18980.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1272+291G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097582 | |||||||
| chr2:112097712 | C | CA | 24 | a0001c0001t0001g0238 a0001c0001t0002g0036 a0001c0001t0002g0049 others(21): Show |
24 | HG01069.hp2 HG01109.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1272+446dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr2 | 112097712 | ||||||
| chr2:112097712 | CA | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(148): Show |
161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1272+446delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr2 | 112097712 | ||||||
| chr2:112097731 | A | C | 2 | a0001c0001t0001g0267 a0001c0001t0038g0192 |
2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1272+440A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097731 | |||||||
| chr2:112097737 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1272+446A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097737 | |||||||
| chr2:112097818 | T | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1272+527T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097818 | |||||||
| chr2:112097908 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1272+617A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097908 | |||||||
| chr2:112097956 | C | G | 4 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0001t0007g0092 others(1): Show |
4 | HG01243.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273-639C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097956 | |||||||
| chr2:112097981 | TC | T | 5 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(2): Show |
5 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-613delC | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112097981 | |||||||
| chr2:112098376 | C | T | 21 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0097 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.1273-219C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112098376 | |||||||
| chr2:112098520 | G | A | 1 | a0001c0001t0004g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1273-75G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112098520 | |||||||
| chr2:112098588 | C | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(194): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(205): Show |
splice_region_variant&intron_variant | LOW | c.1273-7C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 13/18 | chr2 | 112098588 | |||||||
| chr2:112098731 | G | A | 6 | a0001c0001t0006g0233 a0001c0001t0006g0234 a0001c0001t0006g0235 others(3): Show |
6 | HG02027.hp2 NA18978.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1376+33G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098731 | |||||||
| chr2:112098745 | C | T | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1376+47C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098745 | |||||||
| chr2:112098749 | T | C | 1 | a0002c0002t0003g0006 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1376+51T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098749 | |||||||
| chr2:112098757 | C | A | 5 | a0002c0002t0004g0116 a0002c0002t0004g0117 a0002c0002t0004g0118 others(2): Show |
5 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376+59C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098757 | |||||||
| chr2:112098790 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1376+92C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098790 | |||||||
| chr2:112098908 | C | T | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1376+210C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098908 | |||||||
| chr2:112098915 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1376+217C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098915 | |||||||
| chr2:112098917 | A | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1376+219A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112098917 | |||||||
| chr2:112099020 | T | C | 1 | a0001c0001t0007g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1376+322T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099020 | |||||||
| chr2:112099178 | C | T | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1376+480C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099178 | |||||||
| chr2:112099351 | T | C | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1376+653T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099351 | |||||||
| chr2:112099499 | G | A | 8 | a0001c0001t0001g0127 a0001c0001t0001g0196 a0001c0001t0001g0225 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1376+801G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099499 | |||||||
| chr2:112099525 | C | CAT | 20 | a0001c0001t0001g0020 a0001c0001t0001g0219 a0001c0001t0001g0228 others(17): Show |
21 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1376+857_1376+858d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | C | CATAT | 6 | a0001c0001t0001g0021 a0001c0001t0002g0040 a0001c0001t0002g0043 others(3): Show |
6 | HG01361.hp1 HG01496.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376+855_1376+858d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | C | CATATAT | 6 | a0001c0001t0002g0097 a0001c0001t0002g0099 a0001c0001t0002g0100 others(3): Show |
6 | HG02698.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376+853_1376+858d others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | C | CATATATA others(1): Show |
5 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0106 others(2): Show |
5 | HG02056.hp1 HG03017.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1376+851_1376+858d others(10): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | C | CATATATA others(3): Show |
6 | a0001c0001t0002g0096 a0001c0001t0002g0105 a0001c0001t0002g0229 others(3): Show |
6 | HG00280.hp1 HG01934.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376+849_1376+858d others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | C | CATATATA others(5): Show |
1 | a0001c0001t0002g0104 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1376+847_1376+858d others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | C | CATATATA others(7): Show |
2 | a0001c0001t0002g0107 a0001c0001t0002g0253 |
2 | HG00140.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1376+845_1376+858d others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | C | CATATATA others(9): Show |
1 | a0001c0001t0002g0098 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1376+843_1376+858d others(18): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | CAT | C | 3 | a0001c0001t0001g0183 a0001c0001t0002g0075 a0001c0001t0011g0230 |
3 | HG02027.hp1 HG02148.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1376+857_1376+858d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | CATATAT | C | 10 | a0001c0001t0026g0022 a0002c0002t0004g0113 a0002c0002t0004g0115 others(7): Show |
10 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1376+853_1376+858d others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099525 | CATATATA others(3): Show |
C | 1 | a0001c0001t0002g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1376+849_1376+858d others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099525 | ||||||
| chr2:112099527 | T | C | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1376+829T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099527 | |||||||
| chr2:112099529 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0039g0201 |
2 | NA18978.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1376+831T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099529 | |||||||
| chr2:112099545 | TATATATA others(5): Show |
T | 2 | a0001c0001t0027g0296 a0003c0003t0009g0301 |
2 | HG02145.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1376+849_1376+860d others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099545 | ||||||
| chr2:112099547 | TATATATA others(3): Show |
T | 18 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(15): Show |
20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1376+851_1376+860d others(12): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099547 | ||||||
| chr2:112099549 | TATATATA others(1): Show |
T | 8 | a0002c0002t0003g0137 a0002c0002t0003g0138 a0002c0002t0003g0140 others(5): Show |
8 | NA18941.hp1 NA18957.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+853_1376+860d others(10): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099549 | ||||||
| chr2:112099551 | TATATAC | T | 52 | a0001c0001t0001g0205 a0001c0001t0013g0282 a0001c0001t0013g0284 others(49): Show |
55 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.1376+855_1376+860d others(8): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099551 | ||||||
| chr2:112099553 | TATAC | T | 8 | a0001c0001t0001g0225 a0001c0001t0001g0272 a0001c0001t0013g0283 others(5): Show |
8 | HG00323.hp2 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+857_1376+860d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099553 | ||||||
| chr2:112099555 | T | C | 5 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0015g0170 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376+857T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099555 | |||||||
| chr2:112099555 | TAC | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(71): Show |
80 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1376+868_1376+869d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099555 | ||||||
| chr2:112099557 | C | T | 18 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0001t0001g0211 others(15): Show |
18 | HG00621.hp2 HG00642.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1376+859C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099557 | |||||||
| chr2:112099854 | G | T | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1377-768G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099854 | |||||||
| chr2:112099882 | C | CA | 49 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0001t0001g0246 others(46): Show |
51 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1377-722dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099882 | ||||||
| chr2:112099882 | CA | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0208 others(10): Show |
13 | HG02056.hp1 HG02109.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.1377-722delA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr2 | 112099882 | ||||||
| chr2:112099956 | T | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1377-666T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112099956 | |||||||
| chr2:112100021 | A | G | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1377-601A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100021 | |||||||
| chr2:112100065 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(171): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1377-557A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100065 | |||||||
| chr2:112100233 | C | T | 1 | a0001c0001t0040g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1377-389C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100233 | |||||||
| chr2:112100288 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(196): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1377-334A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100288 | |||||||
| chr2:112100545 | C | T | 71 | a0002c0002t0001g0025 a0002c0002t0001g0199 a0002c0002t0001g0207 others(68): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1377-77C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 14/18 | chr2 | 112100545 | |||||||
| chr2:112100908 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(97): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1450+213C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112100908 | |||||||
| chr2:112101442 | T | C | 2 | a0002c0002t0003g0172 a0002c0002t0003g0180 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1450+747T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112101442 | |||||||
| chr2:112101442 | T | G | 2 | a0002c0002t0018g0291 a0002c0002t0018g0292 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1450+747T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112101442 | |||||||
| chr2:112101457 | T | G | 3 | a0001c0001t0001g0127 a0001c0001t0002g0285 a0001c0001t0002g0295 |
3 | HG01167.hp2 HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1450+762T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112101457 | |||||||
| chr2:112101617 | T | C | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+922T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112101617 | |||||||
| chr2:112101890 | GACAAGTT others(11): Show |
G | 1 | a0001c0001t0006g0239 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1450+1217_1450+123 others(22): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr2 | 112101890 | ||||||
| chr2:112102007 | T | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1450+1312T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102007 | |||||||
| chr2:112102118 | T | C | 5 | a0001c0001t0007g0029 a0001c0001t0007g0090 a0001c0001t0007g0091 others(2): Show |
5 | HG01243.hp2 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450+1423T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102118 | |||||||
| chr2:112102186 | A | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1450+1491A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102186 | |||||||
| chr2:112102346 | G | GCAAGGCT others(2956): Show |
1 | a0001c0001t0001g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1450+1663_1450+166 others(2967): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr2 | 112102346 | ||||||
| chr2:112102387 | C | T | 2 | a0002c0002t0004g0115 a0002c0002t0004g0119 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1450+1692C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102387 | |||||||
| chr2:112102421 | C | T | 1 | a0001c0001t0034g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1450+1726C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102421 | |||||||
| chr2:112102491 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1450+1796C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102491 | |||||||
| chr2:112102644 | A | C | 2 | a0002c0002t0018g0291 a0002c0002t0018g0292 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1450+1949A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102644 | |||||||
| chr2:112102658 | A | T | 2 | a0001c0001t0004g0088 a0001c0001t0004g0089 |
2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1450+1963A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102658 | |||||||
| chr2:112102733 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG03688.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1450+2038T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102733 | |||||||
| chr2:112102923 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1450+2228C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112102923 | |||||||
| chr2:112103357 | C | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(193): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1451-2645C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103357 | |||||||
| chr2:112103382 | A | G | 1 | a0002c0002t0012g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1451-2620A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103382 | |||||||
| chr2:112103543 | A | C | 1 | a0001c0001t0002g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1451-2459A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103543 | |||||||
| chr2:112103575 | T | G | 2 | a0001c0001t0007g0090 a0001c0001t0007g0092 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1451-2427T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103575 | |||||||
| chr2:112103576 | T | G | 2 | a0001c0001t0007g0090 a0001c0001t0007g0092 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1451-2426T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103576 | |||||||
| chr2:112103578 | T | C | 2 | a0001c0001t0007g0090 a0001c0001t0007g0092 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1451-2424T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103578 | |||||||
| chr2:112103579 | G | T | 2 | a0001c0001t0007g0090 a0001c0001t0007g0092 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1451-2423G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103579 | |||||||
| chr2:112103610 | C | T | 5 | a0002c0002t0001g0207 a0002c0002t0003g0171 a0002c0002t0003g0172 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451-2392C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112103610 | |||||||
| chr2:112104385 | T | C | 1 | a0001c0001t0030g0054 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1451-1617T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112104385 | |||||||
| chr2:112104510 | A | G | 1 | a0001c0001t0011g0230 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1451-1492A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112104510 | |||||||
| chr2:112104575 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1451-1427A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112104575 | |||||||
| chr2:112104642 | G | A | 4 | a0001c0001t0002g0074 a0001c0001t0002g0077 a0001c0001t0002g0079 others(1): Show |
4 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1451-1360G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112104642 | |||||||
| chr2:112105094 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(173): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1451-908T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105094 | |||||||
| chr2:112105218 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0003g0153 |
2 | HG00558.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1451-784C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105218 | |||||||
| chr2:112105317 | G | A | 3 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0043 |
3 | HG01361.hp1 HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1451-685G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105317 | |||||||
| chr2:112105390 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1451-612A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105390 | |||||||
| chr2:112105567 | T | G | 2 | a0001c0001t0001g0021 a0002c0002t0012g0279 |
2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1451-435T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105567 | |||||||
| chr2:112105698 | T | C | 1 | a0002c0002t0004g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1451-304T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105698 | |||||||
| chr2:112105913 | T | C | 2 | a0001c0001t0006g0233 a0001c0001t0006g0239 |
2 | HG02027.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1451-89T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 15/18 | chr2 | 112105913 | |||||||
| chr2:112106161 | C | G | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1524+86C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106161 | |||||||
| chr2:112106225 | T | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1524+150T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106225 | |||||||
| chr2:112106250 | A | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1524+175A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106250 | |||||||
| chr2:112106274 | A | G | 1 | a0002c0002t0004g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1524+199A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106274 | |||||||
| chr2:112106353 | C | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1524+278C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106353 | |||||||
| chr2:112106515 | A | G | 1 | a0001c0005t0020g0290 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1524+440A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106515 | |||||||
| chr2:112106568 | A | AT | 11 | a0001c0001t0001g0195 a0001c0001t0001g0226 a0001c0001t0002g0040 others(8): Show |
11 | HG00323.hp2 HG01978.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+507dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 112106568 | ||||||
| chr2:112106684 | A | G | 5 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(2): Show |
5 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+609A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106684 | |||||||
| chr2:112106792 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(197): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1524+717C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112106792 | |||||||
| chr2:112107085 | C | T | 2 | a0002c0002t0008g0144 a0002c0002t0008g0148 |
2 | HG01255.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1525-703C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107085 | |||||||
| chr2:112107156 | G | A | 1 | a0001c0001t0028g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1525-632G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107156 | |||||||
| chr2:112107290 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(233): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1525-498A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107290 | |||||||
| chr2:112107317 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0218 a0001c0001t0001g0221 |
3 | NA18747.hp2 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1525-471C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107317 | |||||||
| chr2:112107357 | C | CA | 36 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0001g0193 others(33): Show |
37 | HG00140.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1525-412dupA | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 112107357 | ||||||
| chr2:112107357 | C | CAA | 69 | a0001c0001t0001g0203 a0001c0001t0001g0209 a0001c0001t0001g0215 others(66): Show |
73 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.1525-413_1525-412d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 112107357 | ||||||
| chr2:112107396 | A | AT | 8 | a0001c0001t0001g0215 a0002c0002t0003g0138 a0002c0002t0003g0140 others(5): Show |
8 | NA18957.hp1 NA18957.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-384dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr2 | 112107396 | ||||||
| chr2:112107496 | A | G | 1 | a0001c0001t0038g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1525-292A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107496 | |||||||
| chr2:112107514 | G | T | 1 | a0001c0001t0001g0245 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1525-274G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107514 | |||||||
| chr2:112107677 | A | G | 5 | a0002c0002t0001g0207 a0002c0002t0003g0171 a0002c0002t0003g0172 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-111A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 16/18 | chr2 | 112107677 | |||||||
| chr2:112107886 | G | A | 1 | a0001c0001t0005g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1577+46G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112107886 | |||||||
| chr2:112107953 | T | G | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1577+113T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112107953 | |||||||
| chr2:112108055 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG03688.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1577+215G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108055 | |||||||
| chr2:112108089 | A | G | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1577+249A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108089 | |||||||
| chr2:112108262 | A | G | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1577+422A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108262 | |||||||
| chr2:112108393 | T | C | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1577+553T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108393 | |||||||
| chr2:112108527 | A | C | 1 | a0001c0001t0002g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1577+687A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108527 | |||||||
| chr2:112108646 | T | C | 3 | a0002c0002t0004g0030 a0002c0002t0004g0130 a0002c0002t0004g0132 |
3 | HG03195.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1577+806T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108646 | |||||||
| chr2:112108743 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0003g0153 |
2 | HG00558.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1577+903C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108743 | |||||||
| chr2:112108926 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0185 |
3 | NA18980.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1577+1086C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108926 | |||||||
| chr2:112108981 | T | C | 20 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(17): Show |
23 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1577+1141T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112108981 | |||||||
| chr2:112109020 | A | T | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1180A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109020 | |||||||
| chr2:112109068 | G | A | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1228G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109068 | |||||||
| chr2:112109129 | AT | A | 4 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0006g0249 others(1): Show |
4 | NA18992.hp1 NA19003.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1292delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109129 | ||||||
| chr2:112109272 | C | A | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+1432C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109272 | |||||||
| chr2:112109409 | T | C | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1577+1569T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109409 | |||||||
| chr2:112109425 | C | T | 5 | a0001c0001t0007g0029 a0001c0001t0007g0090 a0001c0001t0007g0091 others(2): Show |
5 | HG01243.hp2 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1577+1585C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109425 | |||||||
| chr2:112109664 | C | CT | 23 | a0001c0001t0001g0041 a0001c0001t0001g0217 a0001c0001t0001g0232 others(20): Show |
24 | HG01109.hp1 HG01109.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1577+1846dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109664 | ||||||
| chr2:112109664 | CT | C | 10 | a0001c0001t0001g0248 a0001c0001t0002g0062 a0001c0001t0005g0260 others(7): Show |
10 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1577+1846delT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109664 | ||||||
| chr2:112109664 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0007g0090 a0001c0001t0007g0092 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1577+1836_1577+184 others(15): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109664 | ||||||
| chr2:112109699 | T | C | 5 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0015g0170 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1577+1859T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109699 | |||||||
| chr2:112109759 | C | CT | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
126 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1577+1939dupT | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109759 | ||||||
| chr2:112109759 | C | CTT | 9 | a0001c0001t0001g0211 a0001c0001t0001g0215 a0001c0001t0001g0238 others(6): Show |
9 | HG01192.hp2 HG01517.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1577+1938_1577+193 others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112109759 | ||||||
| chr2:112109828 | G | A | 1 | a0002c0002t0001g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1577+1988G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109828 | |||||||
| chr2:112109915 | C | T | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577+2075C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109915 | |||||||
| chr2:112109982 | C | T | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1577+2142C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112109982 | |||||||
| chr2:112110270 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1577+2430C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110270 | |||||||
| chr2:112110358 | T | C | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1577+2518T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110358 | |||||||
| chr2:112110584 | C | A | 9 | a0001c0001t0007g0029 a0001c0001t0007g0090 a0001c0001t0007g0091 others(6): Show |
9 | HG00323.hp2 HG01243.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1578-2315C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110584 | |||||||
| chr2:112110732 | G | A | 5 | a0001c0001t0004g0088 a0001c0001t0004g0089 a0001c0001t0015g0170 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578-2167G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110732 | |||||||
| chr2:112110738 | C | G | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0013g0284 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-2161C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110738 | |||||||
| chr2:112110780 | A | G | 2 | a0002c0002t0008g0144 a0002c0002t0008g0148 |
2 | HG01255.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1578-2119A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110780 | |||||||
| chr2:112110791 | A | G | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1578-2108A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110791 | |||||||
| chr2:112110836 | G | A | 5 | a0001c0001t0007g0090 a0001c0001t0007g0092 a0001c0001t0011g0184 others(2): Show |
5 | HG01243.hp2 HG02922.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578-2063G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110836 | |||||||
| chr2:112110849 | G | A | 28 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(25): Show |
30 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1578-2050G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110849 | |||||||
| chr2:112110892 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1578-2007G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112110892 | |||||||
| chr2:112111271 | C | G | 1 | a0002c0002t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1578-1628C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111271 | |||||||
| chr2:112111464 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(206): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1578-1435C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111464 | |||||||
| chr2:112111695 | GTGGAAAT others(31): Show |
G | 1 | a0002c0002t0001g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1578-1202_1578-116 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr2 | 112111695 | ||||||
| chr2:112111869 | G | A | 2 | a0001c0001t0002g0123 a0001c0001t0002g0229 |
2 | HG02257.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1578-1030G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111869 | |||||||
| chr2:112111889 | A | G | 4 | a0001c0004t0010g0286 a0001c0004t0010g0287 a0001c0004t0010g0288 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1578-1010A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111889 | |||||||
| chr2:112111995 | C | T | 1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1578-904C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112111995 | |||||||
| chr2:112112038 | A | T | 1 | a0001c0005t0020g0290 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1578-861A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112038 | |||||||
| chr2:112112185 | C | G | 23 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0097 others(20): Show |
23 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1578-714C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112185 | |||||||
| chr2:112112278 | G | C | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1578-621G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112278 | |||||||
| chr2:112112284 | C | T | 5 | a0002c0002t0001g0025 a0002c0002t0012g0278 a0002c0002t0012g0280 others(2): Show |
5 | HG02451.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578-615C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112284 | |||||||
| chr2:112112431 | C | T | 6 | a0002c0002t0004g0024 a0002c0002t0004g0032 a0002c0002t0004g0033 others(3): Show |
6 | HG01175.hp1 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1578-468C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112431 | |||||||
| chr2:112112448 | A | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0185 |
3 | NA18980.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1578-451A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112448 | |||||||
| chr2:112112467 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1578-432C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112467 | |||||||
| chr2:112112539 | A | G | 2 | a0001c0001t0026g0022 a0001c0001t0042g0297 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1578-360A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112539 | |||||||
| chr2:112112596 | G | C | 5 | a0001c0001t0007g0029 a0001c0001t0007g0090 a0001c0001t0007g0091 others(2): Show |
5 | HG01243.hp2 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578-303G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112596 | |||||||
| chr2:112112724 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1578-175A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112724 | |||||||
| chr2:112112832 | C | T | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1578-67C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 17/18 | chr2 | 112112832 | |||||||
| chr2:112112973 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1608+44C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112112973 | |||||||
| chr2:112113042 | CAG | C | 4 | a0001c0001t0011g0184 a0001c0001t0011g0206 a0001c0001t0011g0216 others(1): Show |
4 | HG02922.hp1 HG02965.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+115_1608+116d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113042 | ||||||
| chr2:112113125 | ATACT | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(169): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1608+201_1608+204d others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113125 | ||||||
| chr2:112113153 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(230): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1608+224G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113153 | |||||||
| chr2:112113424 | C | A | 2 | a0001c0001t0002g0285 a0001c0001t0002g0295 |
2 | HG01167.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1608+495C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113424 | |||||||
| chr2:112113564 | GGGATGGG others(7): Show |
G | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1608+637_1608+650d others(16): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113564 | ||||||
| chr2:112113573 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1608+644A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113573 | |||||||
| chr2:112113575 | G | T | 1 | a0001c0001t0002g0061 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1608+646G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113575 | |||||||
| chr2:112113578 | T | A | 1 | a0001c0001t0002g0061 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1608+649T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113578 | |||||||
| chr2:112113610 | CAAGATTC others(31): Show |
C | 2 | a0001c0001t0026g0022 a0001c0005t0020g0290 |
2 | HG01109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1608+782_1608+819d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113610 | ||||||
| chr2:112113617 | C | G | 1 | a0001c0001t0002g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1608+688C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113617 | |||||||
| chr2:112113700 | CTACAGAA others(11): Show |
C | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+783_1608+800d others(20): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113700 | ||||||
| chr2:112113711 | T | G | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1608+782T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113711 | |||||||
| chr2:112113735 | A | C | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+806A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113735 | |||||||
| chr2:112113736 | C | T | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+807C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113736 | |||||||
| chr2:112113749 | G | T | 3 | a0001c0001t0005g0131 a0001c0001t0015g0174 a0001c0001t0042g0297 |
3 | HG02055.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1608+820G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113749 | |||||||
| chr2:112113749 | GGTAGCAT others(31): Show |
G | 3 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0001t0013g0283 |
3 | HG00323.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1608+896_1608+933d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113749 | ||||||
| chr2:112113761 | G | GAAAGATT others(69): Show |
1 | a0001c0001t0013g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1608+895_1608+896i others(78): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113761 | ||||||
| chr2:112113785 | GATGTAGC others(33): Show |
G | 1 | a0001c0001t0005g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1608+857_1608+896d others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113785 | |||||||
| chr2:112113787 | T | G | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+858T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113787 | |||||||
| chr2:112113787 | TGTAGCAT others(107): Show |
T | 5 | a0001c0001t0005g0011 a0001c0001t0005g0257 a0001c0001t0005g0259 others(2): Show |
6 | HG00639.hp1 HG01243.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608+972_1608+1085 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113787 | ||||||
| chr2:112113787 | TGTAGCAT others(183): Show |
T | 1 | a0001c0001t0028g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1608+934_1608+1123 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113787 | ||||||
| chr2:112113825 | T | G | 6 | a0001c0001t0007g0029 a0001c0001t0007g0092 a0001c0001t0007g0114 others(3): Show |
6 | HG01243.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+896T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113825 | |||||||
| chr2:112113825 | TGTAGCAT others(31): Show |
T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(167): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1608+972_1608+1009 others(41): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113825 | ||||||
| chr2:112113825 | TGTAGCAT others(1361): Show |
T | 1 | a0002c0002t0004g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1608+972_1609-816d others(2): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113825 | ||||||
| chr2:112113837 | G | A | 5 | a0001c0001t0007g0029 a0001c0001t0007g0092 a0001c0001t0007g0114 others(2): Show |
5 | HG01243.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1608+908G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113837 | |||||||
| chr2:112113863 | G | GGTAGCAT others(31): Show |
2 | a0001c0001t0001g0127 a0001c0001t0027g0296 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1608+971_1608+972i others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113863 | ||||||
| chr2:112113863 | G | T | 8 | a0001c0001t0002g0061 a0001c0001t0007g0029 a0001c0001t0007g0092 others(5): Show |
8 | HG01243.hp2 HG02132.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1608+934G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113863 | |||||||
| chr2:112113875 | G | A | 3 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0001t0013g0283 |
3 | HG00323.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1608+946G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113875 | |||||||
| chr2:112113901 | G | GGTAGCAT others(69): Show |
1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1608+1047_1608+104 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113901 | ||||||
| chr2:112113901 | G | T | 49 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(46): Show |
49 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.1608+972G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113901 | |||||||
| chr2:112113901 | GGTAGCAT others(31): Show |
G | 3 | a0002c0002t0003g0169 a0002c0002t0008g0007 a0002c0002t0008g0154 |
4 | HG01109.hp1 HG01515.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+1010_1608+104 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113901 | ||||||
| chr2:112113901 | GGTAGCAT others(107): Show |
G | 1 | a0001c0001t0005g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1608+1048_1608+116 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113901 | ||||||
| chr2:112113903 | T | TAGCATTA others(6): Show |
1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+981_1608+982i others(15): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113903 | ||||||
| chr2:112113925 | ACTCTACA others(33): Show |
A | 2 | a0002c0002t0004g0117 a0002c0002t0004g0118 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1608+999_1608+1038 others(43): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113925 | ||||||
| chr2:112113939 | T | G | 43 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(40): Show |
43 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.1608+1010T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113939 | |||||||
| chr2:112113949 | C | T | 12 | a0001c0001t0005g0087 a0001c0001t0005g0124 a0001c0001t0005g0125 others(9): Show |
13 | HG01070.hp2 HG01346.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1608+1020C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113949 | |||||||
| chr2:112113971 | G | T | 1 | a0001c0001t0002g0073 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1042G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113971 | |||||||
| chr2:112113973 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1044A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113973 | |||||||
| chr2:112113977 | G | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
44 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1608+1048G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113977 | |||||||
| chr2:112113977 | GGTAGCAT others(31): Show |
G | 13 | a0001c0001t0001g0038 a0001c0001t0002g0035 a0001c0001t0002g0036 others(10): Show |
13 | HG00323.hp1 HG01175.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1608+1314_1608+135 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113977 | ||||||
| chr2:112113977 | GGTAGCAT others(69): Show |
G | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1608+1276_1608+135 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112113977 | ||||||
| chr2:112113983 | A | T | 1 | a0001c0001t0002g0073 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1054A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113983 | |||||||
| chr2:112113984 | T | A | 1 | a0001c0001t0002g0073 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1055T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113984 | |||||||
| chr2:112113984 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1055T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113984 | |||||||
| chr2:112113986 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1057A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113986 | |||||||
| chr2:112113986 | A | T | 1 | a0001c0001t0002g0073 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1608+1057A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112113986 | |||||||
| chr2:112114010 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1608+1081A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114010 | |||||||
| chr2:112114015 | T | G | 5 | a0001c0001t0002g0045 a0001c0001t0002g0073 a0001c0001t0007g0090 others(2): Show |
5 | HG00558.hp1 HG03239.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608+1086T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114015 | |||||||
| chr2:112114021 | A | T | 1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+1092A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114021 | |||||||
| chr2:112114022 | T | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
7 | HG02165.hp1 HG02886.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1608+1093T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114022 | |||||||
| chr2:112114022 | T | TACGAAGC others(13): Show |
1 | a0001c0001t0015g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1608+1093_1608+109 others(24): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114022 | |||||||
| chr2:112114025 | C | T | 6 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0257 others(3): Show |
7 | HG00639.hp1 HG01243.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1608+1096C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114025 | |||||||
| chr2:112114032 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1608+1103A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114032 | |||||||
| chr2:112114046 | A | C | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1117A>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114046 | |||||||
| chr2:112114047 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1118G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114047 | |||||||
| chr2:112114048 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1119A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114048 | |||||||
| chr2:112114053 | T | G | 7 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0257 others(4): Show |
8 | HG00639.hp1 HG01243.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+1124T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114053 | |||||||
| chr2:112114060 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(141): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1608+1131T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114060 | |||||||
| chr2:112114075 | T | C | 1 | a0001c0001t0026g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1608+1146T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114075 | |||||||
| chr2:112114085 | G | C | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1156G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114085 | |||||||
| chr2:112114091 | T | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0061 others(3): Show |
6 | HG02055.hp2 HG02132.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+1162T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114091 | |||||||
| chr2:112114093 | T | G | 1 | a0001c0001t0002g0045 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1608+1164T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114093 | |||||||
| chr2:112114098 | T | C | 10 | a0001c0001t0001g0038 a0002c0002t0004g0024 a0002c0002t0004g0032 others(7): Show |
10 | HG00323.hp1 HG01175.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1608+1169T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114098 | |||||||
| chr2:112114104 | AAAGATTC others(867): Show |
A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0002c0002t0012g0279 |
3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1608+1200_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114104 | ||||||
| chr2:112114110 | T | G | 2 | a0002c0002t0003g0172 a0002c0002t0003g0180 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1608+1181T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114110 | |||||||
| chr2:112114113 | T | C | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1608+1184T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114113 | |||||||
| chr2:112114115 | ACTCTACA others(375): Show |
A | 1 | a0001c0001t0005g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1608+1189_1608+157 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114115 | ||||||
| chr2:112114129 | T | G | 7 | a0001c0001t0025g0111 a0002c0002t0003g0139 a0002c0002t0003g0145 others(4): Show |
7 | HG03239.hp2 NA18984.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.1608+1200T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114129 | |||||||
| chr2:112114167 | T | TGTAGCAT others(107): Show |
1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1275_1608+127 others(118): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114167 | ||||||
| chr2:112114174 | T | C | 1 | a0002c0002t0003g0165 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1608+1245T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114174 | |||||||
| chr2:112114205 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1276T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114205 | |||||||
| chr2:112114205 | T | G | 2 | a0001c0001t0013g0283 a0001c0001t0013g0284 |
2 | HG00323.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1608+1276T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114205 | |||||||
| chr2:112114205 | T | TGTAGCAT others(69): Show |
2 | a0001c0001t0002g0095 a0001c0001t0002g0112 |
2 | NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1608+1313_1608+131 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114205 | ||||||
| chr2:112114205 | TGTAGCAT others(107): Show |
T | 1 | a0002c0002t0003g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1608+1352_1608+146 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114205 | ||||||
| chr2:112114205 | TGTAGCAT others(221): Show |
T | 1 | a0001c0001t0007g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1608+1352_1609-157 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114205 | ||||||
| chr2:112114212 | T | C | 5 | a0002c0002t0003g0139 a0002c0002t0003g0145 a0002c0002t0003g0167 others(2): Show |
5 | NA18987.hp1 NA18995.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608+1283T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114212 | |||||||
| chr2:112114238 | AAAGATGT others(34): Show |
A | 1 | a0002c0002t0003g0157 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1608+1311_1608+135 others(45): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114238 | ||||||
| chr2:112114243 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1314T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114243 | |||||||
| chr2:112114243 | T | G | 45 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(42): Show |
45 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1608+1314T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114243 | |||||||
| chr2:112114243 | TGTAGCAT others(31): Show |
T | 3 | a0001c0001t0001g0027 a0001c0001t0007g0091 a0002c0002t0003g0181 |
3 | HG02280.hp2 HG03579.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1608+1390_1608+142 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114243 | ||||||
| chr2:112114243 | TGTAGCAT others(69): Show |
T | 1 | a0002c0002t0003g0176 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1608+1352_1608+142 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114243 | ||||||
| chr2:112114243 | TGTAGCAT others(145): Show |
T | 3 | a0002c0002t0003g0139 a0002c0002t0003g0165 a0002c0002t0003g0167 |
3 | NA18947.hp2 NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1608+1352_1608+150 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114243 | ||||||
| chr2:112114281 | G | C | 2 | a0001c0001t0002g0095 a0001c0001t0002g0112 |
2 | NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1608+1352G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114281 | |||||||
| chr2:112114281 | G | T | 25 | a0001c0001t0002g0073 a0001c0001t0005g0011 a0001c0001t0005g0031 others(22): Show |
27 | HG00558.hp1 HG00639.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1608+1352G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114281 | |||||||
| chr2:112114319 | G | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(7): Show |
10 | HG02886.hp1 HG02970.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608+1390G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114319 | |||||||
| chr2:112114319 | G | T | 31 | a0001c0001t0002g0061 a0001c0001t0002g0094 a0001c0001t0002g0096 others(28): Show |
31 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1608+1390G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114319 | |||||||
| chr2:112114319 | GGTAGCAT others(31): Show |
G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(62): Show |
67 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1608+1428_1608+146 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114319 | ||||||
| chr2:112114319 | GGTAGCAT others(69): Show |
G | 1 | a0002c0002t0004g0117 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1608+1428_1608+150 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114319 | ||||||
| chr2:112114319 | GGTAGCAT others(145): Show |
G | 1 | a0001c0005t0020g0290 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1608+1466_1609-153 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114319 | ||||||
| chr2:112114319 | GGTAGCAT others(1055): Show |
G | 1 | a0001c0001t0001g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1608+1466_1609-628 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114319 | ||||||
| chr2:112114326 | T | C | 1 | a0002c0002t0003g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1608+1397T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114326 | |||||||
| chr2:112114357 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1608+1428T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114357 | |||||||
| chr2:112114357 | T | G | 33 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0005g0011 others(30): Show |
35 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1608+1428T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114357 | |||||||
| chr2:112114357 | T | TGTAGCAT others(31): Show |
1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1608+1465_1608+146 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114357 | ||||||
| chr2:112114357 | TGTAGCAT others(31): Show |
G | 1 | a0001c0001t0026g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1608+1428_1608+146 others(47): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114357 | |||||||
| chr2:112114357 | TGTAGCAT others(69): Show |
G | 2 | a0001c0001t0007g0029 a0001c0001t0007g0114 |
2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1608+1428_1608+150 others(85): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114357 | |||||||
| chr2:112114357 | TGTAGCAT others(69): Show |
T | 2 | a0001c0001t0005g0258 a0001c0001t0013g0283 |
2 | HG00323.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1608+1466_1608+154 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114357 | ||||||
| chr2:112114381 | ACTCTACA others(33): Show |
A | 1 | a0002c0002t0004g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1608+1455_1608+149 others(44): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114381 | ||||||
| chr2:112114395 | C | G | 24 | a0001c0001t0001g0127 a0001c0001t0005g0011 a0001c0001t0005g0031 others(21): Show |
26 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1608+1466C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114395 | |||||||
| chr2:112114395 | C | T | 4 | a0001c0001t0013g0284 a0002c0002t0003g0163 a0002c0002t0003g0176 others(1): Show |
4 | HG03669.hp2 NA18984.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+1466C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114395 | |||||||
| chr2:112114395 | CGTAGCAT others(107): Show |
T | 1 | a0002c0002t0003g0145 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1608+1466_1609-157 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114395 | |||||||
| chr2:112114403 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1608+1474T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114403 | |||||||
| chr2:112114408 | AAAGATTC others(563): Show |
A | 2 | a0001c0004t0010g0286 a0001c0004t0010g0287 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1608+1504_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114408 | ||||||
| chr2:112114433 | C | CGTAGCAT others(145): Show |
2 | a0001c0004t0010g0288 a0001c0004t0010g0289 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1608+1541_1608+154 others(156): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | ||||||
| chr2:112114433 | C | CGTAGCAT others(601): Show |
1 | a0002c0002t0003g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1608+1541_1608+154 others(612): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | ||||||
| chr2:112114433 | C | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(7): Show |
10 | HG02109.hp1 HG02165.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1608+1504C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114433 | |||||||
| chr2:112114433 | C | T | 46 | a0001c0001t0002g0034 a0001c0001t0002g0094 a0001c0001t0002g0096 others(43): Show |
48 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.1608+1504C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114433 | |||||||
| chr2:112114433 | CGTAGCAT others(31): Show |
C | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1609-1537_1609-150 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | ||||||
| chr2:112114433 | CGTAGCAT others(31): Show |
T | 1 | a0002c0002t0003g0163 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1608+1504_1608+154 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114433 | |||||||
| chr2:112114433 | CGTAGCAT others(69): Show |
C | 4 | a0001c0001t0001g0187 a0001c0001t0001g0302 a0002c0002t0004g0115 others(1): Show |
4 | HG02145.hp1 HG02572.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-1575_1609-150 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | ||||||
| chr2:112114433 | CGTAGCAT others(221): Show |
C | 5 | a0001c0001t0001g0209 a0002c0002t0003g0143 a0002c0002t0003g0158 others(2): Show |
5 | HG01109.hp1 HG02735.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1608+1542_1609-138 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114433 | ||||||
| chr2:112114471 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(133): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1608+1542T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114471 | |||||||
| chr2:112114471 | T | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(46): Show |
51 | HG00408.hp1 HG00738.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.1608+1542T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114471 | |||||||
| chr2:112114497 | T | TCTACAGA others(865): Show |
2 | a0001c0001t0002g0099 a0001c0001t0002g0100 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1609-1538_1609-153 others(876): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114497 | ||||||
| chr2:112114509 | T | C | 38 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0127 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1609-1575T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114509 | |||||||
| chr2:112114509 | T | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(125): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1609-1575T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114509 | |||||||
| chr2:112114510 | GTAGCATT others(30): Show |
G | 1 | a0001c0001t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1609-1573_1609-153 others(41): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114510 | |||||||
| chr2:112114547 | T | C | 9 | a0001c0001t0001g0127 a0001c0001t0001g0187 a0001c0001t0001g0302 others(6): Show |
9 | HG01256.hp2 HG01258.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1609-1537T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114547 | |||||||
| chr2:112114547 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(145): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1609-1537T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114547 | |||||||
| chr2:112114585 | G | C | 6 | a0002c0002t0003g0171 a0002c0002t0003g0172 a0002c0002t0003g0176 others(3): Show |
6 | HG01257.hp1 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1609-1499G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114585 | |||||||
| chr2:112114585 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1609-1499G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114585 | |||||||
| chr2:112114609 | ACT | A | 18 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(15): Show |
20 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1609-1472_1609-147 others(6): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114609 | ||||||
| chr2:112114623 | G | C | 5 | a0002c0002t0001g0207 a0002c0002t0003g0145 a0002c0002t0003g0165 others(2): Show |
5 | HG02257.hp1 NA18947.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-1461G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114623 | |||||||
| chr2:112114623 | G | T | 56 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0218 others(53): Show |
56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1609-1461G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114623 | |||||||
| chr2:112114636 | AAAGATTC others(335): Show |
A | 31 | a0002c0002t0001g0025 a0002c0002t0003g0005 a0002c0002t0003g0006 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1609-1423_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114636 | ||||||
| chr2:112114661 | T | C | 8 | a0002c0002t0003g0139 a0002c0002t0003g0145 a0002c0002t0003g0157 others(5): Show |
8 | NA18947.hp2 NA18984.hp2 NA18987.hp1 others(5): Show |
intron_variant | MODIFIER | c.1609-1423T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114661 | |||||||
| chr2:112114661 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(166): Show |
177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1609-1423T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114661 | |||||||
| chr2:112114674 | AAAGATTC others(297): Show |
A | 28 | a0001c0001t0001g0218 a0001c0001t0001g0221 a0002c0002t0001g0199 others(25): Show |
28 | HG00323.hp1 HG01081.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.1609-1271_1609-968 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114674 | ||||||
| chr2:112114674 | AAAGATTC others(335): Show |
A | 1 | a0002c0002t0003g0171 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1609-1271_1609-930 others(3): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114674 | ||||||
| chr2:112114699 | G | C | 11 | a0001c0001t0001g0209 a0002c0002t0003g0139 a0002c0002t0003g0143 others(8): Show |
11 | HG01109.hp1 HG02735.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.1609-1385G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114699 | |||||||
| chr2:112114699 | G | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(45): Show |
50 | HG00408.hp1 HG00738.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.1609-1385G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114699 | |||||||
| chr2:112114712 | AAAGATTC others(259): Show |
A | 1 | a0002c0002t0004g0117 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1609-1271_1609-100 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114712 | ||||||
| chr2:112114728 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1609-1356A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114728 | |||||||
| chr2:112114737 | G | C | 5 | a0002c0002t0003g0139 a0002c0002t0003g0145 a0002c0002t0003g0163 others(2): Show |
5 | NA18947.hp2 NA18984.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1609-1347G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114737 | |||||||
| chr2:112114737 | G | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(85): Show |
93 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1609-1347G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114737 | |||||||
| chr2:112114775 | G | C | 3 | a0002c0002t0003g0139 a0002c0002t0003g0163 a0002c0002t0003g0167 |
3 | NA18984.hp2 NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1609-1309G>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114775 | |||||||
| chr2:112114775 | G | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(78): Show |
83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1609-1309G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114775 | |||||||
| chr2:112114788 | AAAGATTC others(183): Show |
A | 2 | a0002c0002t0004g0115 a0002c0002t0004g0119 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1609-1271_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114788 | ||||||
| chr2:112114813 | T | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(55): Show |
60 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1609-1271T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114813 | |||||||
| chr2:112114826 | AAAGATTC others(145): Show |
A | 1 | a0002c0002t0003g0181 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1609-1233_1609-108 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114826 | ||||||
| chr2:112114851 | T | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
55 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.1609-1233T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114851 | |||||||
| chr2:112114851 | T | TGTAGCAT others(31): Show |
1 | a0001c0001t0002g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1609-1157_1609-112 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114851 | ||||||
| chr2:112114851 | TGTAGCAT others(31): Show |
T | 4 | a0001c0001t0013g0282 a0001c0001t0013g0283 a0001c0001t0024g0019 others(1): Show |
4 | HG00323.hp2 HG02723.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-1157_1609-112 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114851 | ||||||
| chr2:112114858 | T | TCGACCTA others(3): Show |
1 | a0001c0001t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1609-1226_1609-122 others(14): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114858 | |||||||
| chr2:112114864 | AAAGATTC others(107): Show |
A | 6 | a0001c0001t0001g0014 a0001c0001t0036g0028 a0002c0002t0003g0158 others(3): Show |
6 | HG01109.hp1 HG02735.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609-1119_1609-100 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114864 | ||||||
| chr2:112114889 | G | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(44): Show |
49 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1609-1195G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114889 | |||||||
| chr2:112114902 | AAAGATTC others(69): Show |
A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(36): Show |
41 | HG00408.hp1 HG00738.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1609-1119_1609-104 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114902 | ||||||
| chr2:112114902 | AAAGATTC others(107): Show |
A | 1 | a0002c0002t0003g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1609-1119_1609-100 others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114902 | ||||||
| chr2:112114927 | G | GGTAGCAT others(31): Show |
1 | a0001c0001t0027g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1609-1144_1609-110 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114927 | ||||||
| chr2:112114927 | G | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0026 others(45): Show |
50 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1609-1157G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114927 | |||||||
| chr2:112114935 | T | C | 2 | a0001c0004t0010g0288 a0001c0004t0010g0289 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1609-1149T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114935 | |||||||
| chr2:112114940 | AAAGATTC others(31): Show |
A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(52): Show |
57 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1609-1119_1609-108 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114940 | ||||||
| chr2:112114940 | AAAGATTC others(69): Show |
A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0268 a0002c0002t0003g0145 |
3 | HG04115.hp2 NA18974.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1609-1119_1609-104 others(80): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114940 | ||||||
| chr2:112114949 | T | C | 1 | a0001c0001t0042g0297 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1609-1135T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114949 | |||||||
| chr2:112114965 | T | G | 37 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0026 others(34): Show |
37 | HG00140.hp2 HG00280.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1609-1119T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114965 | |||||||
| chr2:112114965 | T | TGTAGCAT others(31): Show |
4 | a0001c0001t0001g0127 a0001c0001t0002g0058 a0001c0001t0002g0099 others(1): Show |
4 | HG02109.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-1107_1609-110 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114965 | ||||||
| chr2:112114965 | TGTAGCAT others(31): Show |
T | 2 | a0001c0001t0001g0302 a0001c0001t0026g0022 |
2 | HG03453.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1609-1106_1609-106 others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112114965 | ||||||
| chr2:112114978 | G | A | 128 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0026 others(125): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1609-1106G>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112114978 | |||||||
| chr2:112115071 | C | A | 4 | a0002c0002t0001g0199 a0002c0002t0001g0222 a0002c0002t0003g0141 others(1): Show |
4 | HG02056.hp2 HG04115.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1609-1013C>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115071 | |||||||
| chr2:112115079 | G | T | 1 | a0001c0001t0007g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1609-1005G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115079 | |||||||
| chr2:112115117 | G | T | 1 | a0001c0001t0013g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1609-967G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115117 | |||||||
| chr2:112115141 | ACTCTACA others(33): Show |
A | 1 | a0001c0001t0001g0209 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1609-940_1609-901d others(42): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115141 | ||||||
| chr2:112115155 | G | T | 4 | a0001c0001t0005g0131 a0001c0001t0007g0029 a0001c0001t0007g0091 others(1): Show |
4 | HG02055.hp2 HG03098.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-929G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115155 | |||||||
| chr2:112115155 | GGTAGCAT others(107): Show |
G | 1 | a0001c0001t0007g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1609-891_1609-778d others(2): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115155 | ||||||
| chr2:112115193 | G | T | 4 | a0001c0001t0001g0225 a0001c0001t0002g0212 a0001c0001t0013g0284 others(1): Show |
4 | HG02145.hp2 HG02165.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-891G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115193 | |||||||
| chr2:112115231 | G | T | 25 | a0001c0001t0001g0225 a0001c0001t0002g0212 a0001c0001t0005g0011 others(22): Show |
27 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1609-853G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115231 | |||||||
| chr2:112115231 | GGTAGCAT others(31): Show |
G | 3 | a0001c0001t0001g0250 a0001c0001t0007g0029 a0001c0001t0007g0091 |
3 | HG01074.hp1 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1609-750_1609-713d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115231 | ||||||
| chr2:112115269 | T | G | 31 | a0001c0001t0001g0187 a0001c0001t0001g0246 a0001c0001t0002g0123 others(28): Show |
33 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1609-815T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115269 | |||||||
| chr2:112115269 | T | GGTAGCAT others(31): Show |
1 | a0002c0002t0003g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1609-853_1609-816d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115269 | |||||||
| chr2:112115269 | T | TGTAGCAT others(219): Show |
1 | a0001c0001t0002g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1609-789_1609-788i others(228): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115269 | ||||||
| chr2:112115269 | T | TGTAGCAT others(219): Show |
1 | a0001c0001t0013g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1609-789_1609-788i others(228): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115269 | ||||||
| chr2:112115295 | TCTACAGA others(67): Show |
T | 2 | a0001c0001t0005g0131 a0001c0001t0042g0297 |
2 | HG02055.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1609-712_1609-639d others(76): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115295 | ||||||
| chr2:112115307 | T | G | 21 | a0001c0001t0002g0212 a0001c0001t0005g0011 a0001c0001t0005g0031 others(18): Show |
23 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1609-777T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115307 | |||||||
| chr2:112115309 | T | G | 4 | a0001c0001t0001g0225 a0002c0002t0014g0151 a0002c0002t0014g0152 others(1): Show |
4 | HG01074.hp2 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-775T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115309 | |||||||
| chr2:112115331 | ACTCTACA others(69): Show |
A | 1 | a0001c0001t0007g0114 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1609-750_1609-675d others(78): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115331 | ||||||
| chr2:112115333 | TCTACAGA others(29): Show |
T | 1 | a0001c0001t0026g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1609-712_1609-677d others(38): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115333 | ||||||
| chr2:112115369 | A | ACT | 25 | a0001c0001t0001g0225 a0001c0001t0002g0212 a0001c0001t0005g0011 others(22): Show |
27 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1609-714_1609-713d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115369 | ||||||
| chr2:112115380 | A | T | 3 | a0001c0001t0007g0029 a0001c0001t0007g0090 a0001c0001t0007g0091 |
3 | HG03098.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1609-704A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115380 | |||||||
| chr2:112115381 | T | G | 1 | a0001c0001t0002g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1609-703T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115381 | |||||||
| chr2:112115383 | T | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(168): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1609-701T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115383 | |||||||
| chr2:112115405 | ACT | A | 5 | a0001c0001t0007g0092 a0001c0001t0013g0282 a0001c0001t0013g0283 others(2): Show |
5 | HG00323.hp2 HG01243.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1609-676_1609-675d others(4): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115405 | ||||||
| chr2:112115418 | A | T | 2 | a0001c0001t0007g0092 a0001c0001t0007g0114 |
2 | HG01243.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1609-666A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115418 | |||||||
| chr2:112115419 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1609-665T>C | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115419 | |||||||
| chr2:112115419 | T | G | 1 | a0001c0001t0002g0212 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1609-665T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115419 | |||||||
| chr2:112115419 | TGTAGCAT others(31): Show |
T | 3 | a0001c0001t0007g0029 a0001c0001t0007g0090 a0001c0001t0007g0091 |
3 | HG03098.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1609-627_1609-590d others(40): Show |
TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr2 | 112115419 | ||||||
| chr2:112115457 | G | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(202): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1609-627G>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115457 | |||||||
| chr2:112115470 | A | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0031 a0001c0001t0005g0087 others(16): Show |
21 | HG00639.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1609-614A>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115470 | |||||||
| chr2:112115604 | A | T | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1609-480A>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115604 | |||||||
| chr2:112115834 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1609-250C>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115834 | |||||||
| chr2:112115834 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1609-250C>T | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115834 | |||||||
| chr2:112115955 | T | A | 1 | a0001c0001t0002g0064 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1609-129T>A | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112115955 | |||||||
| chr2:112116020 | T | G | 1 | a0001c0001t0002g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1609-64T>G | TMEM87B | ENSG00000153214.11 | transcript | ENST00000283206.9 | protein_coding | 18/18 | chr2 | 112116020 |