Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1955 |
| ensemblid | ENSG00000106780.9 |
| hgncid | 3234 |
| symbol | MEGF9 |
| name | multiple EGF like domains 9 |
| refseq_nuc | NM_001080497.3 |
| refseq_prot | NP_001073966.2 |
| ensembl_nuc | ENST00000373930.4 |
| ensembl_prot | ENSP00000363040.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 120600811 |
| end | 120714470 |
| strand | - |
| ver | v1.2 |
| region | chr9:120600811-120714470 |
| region5000 | chr9:120595811-120719470 |
| regionname0 | MEGF9_chr9_120600811_120714470 |
| regionname5000 | MEGF9_chr9_120595811_120719470 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 600 | 150 | 55 | 21 | 61 | 3 | 9 | 43 | MEGF9_chr9_120595811_120719470 | MEGF9 | MNGGA others(595): Show |
chr9 | 120595811 | 120719470 |
| a0002 | 1/0 | 602 | 139 | 33 | 23 | 69 | 3 | 10 | 53 | MEGF9_chr9_120595811_120719470 | MEGF9 | MNGGA others(597): Show |
chr9 | 120595811 | 120719470 |
| a0003 | 0/0 | 602 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | MNGGA others(597): Show |
chr9 | 120595811 | 120719470 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 1800 | 120 | 27 | 20 | 61 | 2 | 9 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1795): Show |
chr9 | 120595811 | 120719470 | ||
| a0001c0003 | 0/0 | 1800 | 23 | 22 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1795): Show |
chr9 | 120595811 | 120719470 | ||
| a0001c0004 | 0/0 | 1800 | 4 | 4 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1795): Show |
chr9 | 120595811 | 120719470 | ||
| a0001c0008 | 0/0 | 1800 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1795): Show |
chr9 | 120595811 | 120719470 | ||
| a0001c0009 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1795): Show |
chr9 | 120595811 | 120719470 | ||
| a0001c0010 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1795): Show |
chr9 | 120595811 | 120719470 | ||
| a0002c0001 | 1/0 | 1806 | 136 | 33 | 21 | 69 | 2 | 10 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1801): Show |
chr9 | 120595811 | 120719470 | ||
| a0002c0005 | 0/0 | 1806 | 2 | 0 | 1 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1801): Show |
chr9 | 120595811 | 120719470 | ||
| a0002c0006 | 0/0 | 1806 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1801): Show |
chr9 | 120595811 | 120719470 | ||
| a0003c0007 | 0/0 | 1806 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | ATGAA others(1801): Show |
chr9 | 120595811 | 120719470 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 6294 | 2 | 1 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0002 | 0/0 | 6294 | 99 | 22 | 17 | 49 | 2 | 9 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0006 | 0/0 | 6294 | 7 | 0 | 0 | 7 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0012 | 0/0 | 6294 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0014 | 0/0 | 6294 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0015 | 0/0 | 6294 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0016 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0020 | 0/1 | 6294 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0021 | 0/0 | 6294 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0023 | 0/0 | 6294 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0002t0024 | 0/0 | 6294 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0003t0003 | 0/0 | 6295 | 9 | 9 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6290): Show |
chr9 | 120595811 | 120719470 |
| a0001c0003t0005 | 0/0 | 6294 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0003t0008 | 0/0 | 6294 | 4 | 4 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0003t0011 | 0/0 | 6294 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0003t0017 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0003t0018 | 0/0 | 6294 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0003t0019 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6290): Show |
chr9 | 120595811 | 120719470 |
| a0001c0003t0027 | 0/0 | 6295 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6290): Show |
chr9 | 120595811 | 120719470 |
| a0001c0004t0005 | 0/0 | 6294 | 4 | 4 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0008t0002 | 0/0 | 6294 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0009t0002 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0001c0010t0005 | 0/0 | 6294 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6289): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0001 | 1/0 | 6300 | 107 | 26 | 15 | 55 | 1 | 9 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0002 | 0/0 | 6300 | 5 | 1 | 3 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0004 | 0/0 | 6300 | 9 | 0 | 0 | 9 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0007 | 0/0 | 6300 | 4 | 3 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0009 | 0/0 | 6300 | 3 | 2 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0010 | 0/0 | 6300 | 3 | 1 | 1 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0013 | 0/0 | 6300 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0022 | 0/0 | 6300 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0025 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0001t0026 | 0/0 | 6300 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0005t0001 | 0/0 | 6300 | 2 | 0 | 1 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0002c0006t0001 | 0/0 | 6300 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| a0003c0007t0001 | 0/0 | 6300 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | AGAGG others(6295): Show |
chr9 | 120595811 | 120719470 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0012g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0012g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0014g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0014g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0015g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0015g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0016g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0020g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0021g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0023g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0002t0024g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0011g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0017g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0018g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0019g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0003t0027g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0004t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0004t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0004t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0004t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0008t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0009t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0001c0010t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0007g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0010g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0010g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0013g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0022g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0025g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0001t0026g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0005t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0002c0006t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| a0003c0007t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0042 | EUR | GBR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0243 | EUR | GBR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00323 | hp1 | a0002 | c0005 | t0001 | g0045 | EUR | FIN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00323 | hp2 | a0001 | c0008 | t0002 | g0163 | EUR | FIN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0023 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0071 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0119 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0108 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00609 | hp1 | a0002 | c0001 | t0004 | g0083 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00639 | hp1 | a0001 | c0003 | t0018 | g0157 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0224 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0256 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0046 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | CHS | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0239 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0047 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00738 | hp1 | a0002 | c0001 | t0002 | g0131 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG00738 | hp2 | a0002 | c0006 | t0001 | g0049 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0056 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0275 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0057 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0015 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01081 | hp2 | a0001 | c0002 | t0021 | g0238 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0107 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01099 | hp2 | a0002 | c0001 | t0010 | g0053 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0051 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0278 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01109 | hp2 | a0002 | c0001 | t0009 | g0100 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01167 | hp1 | a0002 | c0001 | t0002 | g0067 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0061 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0176 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0048 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0050 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01169 | hp2 | a0002 | c0001 | t0002 | g0066 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0058 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0193 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0059 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01243 | hp2 | a0001 | c0002 | t0015 | g0289 | AMR | PUR | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0097 | AMR | CLM | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0270 | AMR | CLM | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0185 | AMR | CLM | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0031 | AMR | CLM | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01496 | hp1 | a0002 | c0001 | t0007 | g0088 | AMR | CLM | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0223 | AMR | CLM | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01884 | hp1 | a0002 | c0001 | t0007 | g0091 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0282 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0141 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0183 | AMR | PEL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01975 | hp2 | a0002 | c0005 | t0001 | g0016 | AMR | PEL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0196 | AMR | PEL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG01981 | hp2 | a0001 | c0002 | t0024 | g0181 | AMR | PEL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0038 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02055 | hp2 | a0002 | c0001 | t0010 | g0095 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0122 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0137 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02132 | hp1 | a0002 | c0001 | t0004 | g0082 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02135 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0073 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02155 | hp1 | a0002 | c0001 | t0001 | g0026 | EAS | CDX | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | CDX | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0121 | EAS | CDX | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | CDX | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0281 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0136 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0214 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0039 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0074 | AMR | PEL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0262 | AMR | PEL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02451 | hp1 | a0001 | c0003 | t0019 | g0148 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02451 | hp2 | a0002 | c0001 | t0001 | g0069 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02523 | hp1 | a0001 | c0002 | t0016 | g0247 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0008 | EAS | KHV | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02572 | hp1 | a0002 | c0001 | t0001 | g0068 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02572 | hp2 | a0001 | c0003 | t0005 | g0162 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02615 | hp2 | a0001 | c0002 | t0012 | g0286 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0276 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02622 | hp2 | a0002 | c0001 | t0001 | g0105 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02630 | hp1 | a0002 | c0001 | t0002 | g0132 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0128 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0144 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0194 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02717 | hp1 | a0001 | c0002 | t0012 | g0287 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02717 | hp2 | a0002 | c0001 | t0007 | g0092 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0098 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02735 | hp1 | a0002 | c0001 | t0022 | g0070 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02738 | hp1 | a0002 | c0001 | t0001 | g0093 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0211 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02809 | hp1 | a0001 | c0003 | t0011 | g0156 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02809 | hp2 | a0001 | c0003 | t0017 | g0149 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0164 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0145 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0143 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02922 | hp1 | a0001 | c0002 | t0015 | g0288 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0044 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02965 | hp1 | a0001 | c0004 | t0005 | g0165 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0036 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02970 | hp1 | a0001 | c0004 | t0005 | g0166 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0064 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0024 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0065 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03041 | hp1 | a0001 | c0003 | t0008 | g0152 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03041 | hp2 | a0001 | c0004 | t0005 | g0168 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03098 | hp1 | a0001 | c0003 | t0008 | g0153 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03098 | hp2 | a0001 | c0010 | t0005 | g0169 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03130 | hp1 | a0001 | c0003 | t0005 | g0161 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03130 | hp2 | a0001 | c0003 | t0003 | g0142 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0089 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03139 | hp2 | a0001 | c0003 | t0011 | g0155 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03195 | hp1 | a0002 | c0001 | t0001 | g0013 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0184 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0147 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0134 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0055 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03225 | hp2 | a0001 | c0003 | t0003 | g0159 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03453 | hp1 | a0001 | c0004 | t0005 | g0167 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03453 | hp2 | a0002 | c0001 | t0001 | g0052 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0269 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0182 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0226 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03516 | hp2 | a0002 | c0001 | t0009 | g0099 | AFR | ESN | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0279 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03540 | hp2 | a0001 | c0003 | t0008 | g0151 | AFR | GWD | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0146 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0172 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0126 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0215 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03704 | hp2 | a0003 | c0007 | t0001 | g0139 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0043 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0268 | SAS | PJL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0170 | SAS | BEB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0034 | SAS | BEB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0192 | SAS | STU | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG04115 | hp2 | a0002 | c0001 | t0001 | g0127 | SAS | STU | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18522 | hp1 | a0002 | c0001 | t0009 | g0101 | AFR | YRI | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18522 | hp2 | a0002 | c0001 | t0001 | g0037 | AFR | YRI | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | CHB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0072 | EAS | CHB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18906 | hp1 | a0001 | c0003 | t0008 | g0150 | AFR | YRI | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0235 | AFR | YRI | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0118 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18943 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18947 | hp2 | a0002 | c0001 | t0026 | g0087 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18949 | hp2 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18954 | hp1 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18962 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18964 | hp1 | a0002 | c0001 | t0002 | g0138 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18964 | hp2 | a0002 | c0001 | t0004 | g0080 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18971 | hp1 | a0001 | c0002 | t0006 | g0266 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0035 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18975 | hp2 | a0001 | c0002 | t0014 | g0199 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18977 | hp1 | a0002 | c0001 | t0013 | g0076 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0041 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18984 | hp1 | a0001 | c0002 | t0006 | g0271 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18986 | hp1 | a0002 | c0001 | t0004 | g0085 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18988 | hp1 | a0001 | c0002 | t0014 | g0255 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18990 | hp2 | a0002 | c0001 | t0013 | g0077 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18993 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18993 | hp2 | a0001 | c0002 | t0023 | g0240 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19003 | hp2 | a0002 | c0001 | t0001 | g0120 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19004 | hp2 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19006 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19009 | hp1 | a0001 | c0002 | t0006 | g0209 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19009 | hp2 | a0002 | c0001 | t0004 | g0081 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0237 | AFR | LWK | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0054 | AFR | LWK | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19060 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19062 | hp1 | a0002 | c0001 | t0004 | g0011 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19065 | hp1 | a0001 | c0002 | t0006 | g0258 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19065 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19066 | hp1 | a0002 | c0001 | t0004 | g0086 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19070 | hp1 | a0002 | c0001 | t0004 | g0079 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19070 | hp2 | a0002 | c0001 | t0025 | g0133 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19074 | hp2 | a0001 | c0002 | t0006 | g0204 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19077 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19078 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19078 | hp2 | a0002 | c0001 | t0004 | g0125 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19085 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19085 | hp2 | a0001 | c0002 | t0006 | g0265 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19086 | hp2 | a0001 | c0002 | t0006 | g0210 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | YRI | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA19240 | hp2 | a0001 | c0002 | t0012 | g0285 | AFR | YRI | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0040 | AFR | ASW | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA20129 | hp2 | a0001 | c0009 | t0002 | g0280 | AFR | ASW | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA20752 | hp1 | a0002 | c0001 | t0010 | g0094 | EUR | TSI | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0267 | EUR | TSI | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02109 | hp1 | a0001 | c0003 | t0003 | g0140 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0135 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0062 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0063 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG02559 | hp2 | a0002 | c0001 | t0001 | g0075 | AFR | ACB | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0277 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG03471 | hp2 | a0001 | c0003 | t0011 | g0154 | AFR | MSL | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG06807 | hp1 | a0001 | c0003 | t0005 | g0160 | AFR | USA | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0129 | AFR | USA | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA20300 | hp1 | a0002 | c0001 | t0007 | g0090 | AFR | USA | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | USA | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA21309 | hp1 | a0002 | c0001 | t0001 | g0096 | AFR | LWK | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| NA21309 | hp2 | a0001 | c0003 | t0027 | g0158 | AFR | LWK | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0020 | g0244 | REF | REF | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0060 | REF | REF | MEGF9_chr9_120595811_120719470 | MEGF9 | chr9 | 120595811 | 120719470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:120713857 | T | C | 1 | a0003 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.502A>G | p.Thr168Ala | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/6 | 614/6300 | 502/1809 | 168/602 | chr9 | 120713857 | |||
| chr9:120714022 | A | C | 1 | a0001 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.337T>G | p.Ser113Ala | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/6 | 449/6300 | 337/1809 | 113/602 | chr9 | 120714022 | |||
| chr9:120714025 | A | C | 1 | a0001 | 23 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(20): Show |
missense_variant | MODERATE | c.334T>G | p.Ser112Ala | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/6 | 446/6300 | 334/1809 | 112/602 | chr9 | 120714025 | |||
| chr9:120714264 | ACGGCGG | A | 1 | a0001 | 149 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(146): Show |
disruptive_inframe_deletion | MODERATE | c.89_94delCCGCCG | p.Ala30_Ala31del | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/6 | 206/6300 | 89/1809 | 30/602 | chr9 | 120714264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:120605274 | C | T | 1 | a0002c0006 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1725G>A | p.Ser575Ser | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1837/6300 | 1725/1809 | 575/602 | chr9 | 120605274 | |||
| chr9:120605403 | C | G | 1 | a0002c0005 | 2 | HG00323.hp1 HG01975.hp2 |
synonymous_variant | LOW | c.1596G>C | p.Val532Val | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1708/6300 | 1596/1809 | 532/602 | chr9 | 120605403 | |||
| chr9:120605592 | G | C | 1 | a0001c0009 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1407C>G | p.Ala469Ala | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1519/6300 | 1407/1809 | 469/602 | chr9 | 120605592 | |||
| chr9:120659454 | G | A | 2 | a0001c0004 a0001c0010 |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.723C>T | p.Gly241Gly | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/6 | 835/6300 | 723/1809 | 241/602 | chr9 | 120659454 | |||
| chr9:120659487 | A | G | 1 | a0001c0004 | 4 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.690T>C | p.Tyr230Tyr | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/6 | 802/6300 | 690/1809 | 230/602 | chr9 | 120659487 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:120600847 | G | A | 4 | a0001c0003t0003 a0001c0003t0017 a0001c0003t0018 others(1): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4343C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 4343 | chr9 | 120600847 | ||||||
| chr9:120600915 | A | C | 1 | a0001c0002t0006 | 7 | NA18971.hp1 NA18984.hp1 NA19009.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4275T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 4275 | chr9 | 120600915 | ||||||
| chr9:120601255 | T | C | 12 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0014 others(9): Show |
122 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*3935A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 3935 | chr9 | 120601255 | ||||||
| chr9:120601414 | T | C | 1 | a0001c0003t0018 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3776A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 3776 | chr9 | 120601414 | ||||||
| chr9:120601796 | G | A | 1 | a0001c0003t0017 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3394C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 3394 | chr9 | 120601796 | ||||||
| chr9:120602098 | C | T | 1 | a0001c0002t0024 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3092G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 3092 | chr9 | 120602098 | ||||||
| chr9:120602164 | C | T | 5 | a0001c0003t0003 a0001c0003t0017 a0001c0003t0018 others(2): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3026G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 3026 | chr9 | 120602164 | ||||||
| chr9:120602223 | C | T | 1 | a0001c0003t0017 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2967G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 2967 | chr9 | 120602223 | ||||||
| chr9:120602291 | C | T | 2 | a0001c0002t0023 a0002c0001t0022 |
2 | HG02735.hp1 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2899G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 2899 | chr9 | 120602291 | ||||||
| chr9:120602365 | C | T | 1 | a0001c0002t0021 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2825G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 2825 | chr9 | 120602365 | ||||||
| chr9:120602507 | C | A | 5 | a0001c0003t0003 a0001c0003t0017 a0001c0003t0018 others(2): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2683G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 2683 | chr9 | 120602507 | ||||||
| chr9:120602773 | G | A | 1 | a0002c0001t0007 | 4 | HG01496.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2417C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 2417 | chr9 | 120602773 | ||||||
| chr9:120602881 | T | C | 1 | a0002c0001t0025 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2309A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 2309 | chr9 | 120602881 | ||||||
| chr9:120603052 | C | T | 4 | a0002c0001t0004 a0002c0001t0010 a0002c0001t0013 others(1): Show |
15 | HG00609.hp1 HG01099.hp2 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2138G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 2138 | chr9 | 120603052 | ||||||
| chr9:120603114 | T | C | 2 | a0001c0003t0008 a0001c0003t0011 |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2076A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 2076 | chr9 | 120603114 | ||||||
| chr9:120603325 | A | G | 1 | a0002c0001t0009 | 3 | HG01109.hp2 HG03516.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1865T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1865 | chr9 | 120603325 | ||||||
| chr9:120603359 | T | C | 3 | a0001c0003t0005 a0001c0004t0005 a0001c0010t0005 |
8 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1831A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1831 | chr9 | 120603359 | ||||||
| chr9:120603400 | C | T | 1 | a0002c0001t0010 | 3 | HG01099.hp2 HG02055.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1790G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1790 | chr9 | 120603400 | ||||||
| chr9:120603516 | T | TC | 3 | a0001c0003t0003 a0001c0003t0019 a0001c0003t0027 |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1673dupG | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1673 | chr9 | 120603516 | ||||||
| chr9:120603586 | T | C | 2 | a0001c0002t0015 a0001c0003t0011 |
5 | HG01243.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1604A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1604 | chr9 | 120603586 | ||||||
| chr9:120603635 | A | G | 5 | a0001c0003t0003 a0001c0003t0017 a0001c0003t0018 others(2): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1555T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 1555 | chr9 | 120603635 | ||||||
| chr9:120604672 | C | T | 1 | a0002c0001t0009 | 3 | HG01109.hp2 HG03516.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*518G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 518 | chr9 | 120604672 | ||||||
| chr9:120604762 | T | C | 1 | a0002c0001t0026 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*428A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 428 | chr9 | 120604762 | ||||||
| chr9:120605000 | C | T | 1 | a0001c0002t0016 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 190 | chr9 | 120605000 | ||||||
| chr9:120605013 | T | A | 1 | a0001c0003t0027 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*177A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 177 | chr9 | 120605013 | ||||||
| chr9:120605048 | T | C | 1 | a0001c0002t0014 | 2 | NA18975.hp2 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*142A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 142 | chr9 | 120605048 | ||||||
| chr9:120605106 | C | T | 3 | a0001c0003t0005 a0001c0004t0005 a0001c0010t0005 |
8 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*84G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 6/6 | 84 | chr9 | 120605106 | ||||||
| chr9:120714446 | G | A | 2 | a0001c0002t0012 a0001c0002t0015 |
5 | HG01243.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-88C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/6 | chr9 | 120714446 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:120606033 | G | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1358-392C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606033 | |||||||
| chr9:120606040 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1358-399G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606040 | |||||||
| chr9:120606049 | G | A | 118 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(115): Show |
119 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1358-408C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606049 | |||||||
| chr9:120606078 | A | G | 2 | a0001c0003t0005g0160 a0001c0003t0005g0161 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1358-437T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606078 | |||||||
| chr9:120606160 | G | T | 1 | a0001c0003t0003g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1358-519C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606160 | |||||||
| chr9:120606170 | C | CA | 18 | a0001c0002t0002g0191 a0001c0002t0002g0211 a0001c0002t0002g0216 others(15): Show |
18 | HG01081.hp2 HG01169.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1358-530dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606170 | |||||||
| chr9:120606170 | CA | C | 25 | a0001c0002t0002g0176 a0001c0002t0002g0276 a0002c0001t0001g0002 others(22): Show |
25 | HG00323.hp1 HG00408.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1358-530delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606170 | |||||||
| chr9:120606170 | CAA | C | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1358-531_1358-530d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606170 | |||||||
| chr9:120606187 | A | C | 1 | a0002c0001t0001g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1358-546T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606187 | |||||||
| chr9:120606214 | G | A | 1 | a0001c0002t0002g0223 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1358-573C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606214 | |||||||
| chr9:120606542 | A | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1358-901T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606542 | |||||||
| chr9:120606633 | C | G | 116 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1358-992G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120606633 | |||||||
| chr9:120607449 | A | G | 9 | a0001c0002t0015g0288 a0001c0002t0015g0289 a0001c0003t0008g0150 others(6): Show |
9 | HG01243.hp2 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1357+292T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120607449 | |||||||
| chr9:120607575 | A | G | 1 | a0002c0001t0001g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1357+166T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 5/5 | chr9 | 120607575 | |||||||
| chr9:120608067 | C | G | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1088-57G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120608067 | |||||||
| chr9:120608263 | T | G | 1 | a0001c0003t0005g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1088-253A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120608263 | |||||||
| chr9:120608456 | T | C | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1088-446A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120608456 | |||||||
| chr9:120608544 | T | C | 180 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1088-534A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120608544 | |||||||
| chr9:120608553 | G | T | 4 | a0002c0001t0007g0088 a0002c0001t0007g0090 a0002c0001t0007g0091 others(1): Show |
4 | HG01496.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1088-543C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120608553 | |||||||
| chr9:120608707 | A | G | 188 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1088-697T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120608707 | |||||||
| chr9:120608730 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1088-720A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120608730 | |||||||
| chr9:120608880 | C | T | 1 | a0001c0002t0002g0273 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1088-870G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120608880 | |||||||
| chr9:120609002 | C | T | 3 | a0001c0002t0002g0212 a0001c0002t0002g0213 a0001c0002t0002g0246 |
3 | HG02129.hp2 NA18942.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1088-992G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120609002 | |||||||
| chr9:120609063 | C | CA | 9 | a0001c0002t0015g0288 a0001c0002t0015g0289 a0001c0003t0008g0150 others(6): Show |
9 | HG01243.hp2 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1088-1054dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120609063 | |||||||
| chr9:120609300 | T | C | 2 | a0001c0003t0005g0160 a0001c0003t0005g0161 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1088-1290A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120609300 | |||||||
| chr9:120609305 | CTCTT | C | 176 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1088-1299_1088-129 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120609305 | |||||||
| chr9:120609506 | T | C | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1088-1496A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120609506 | |||||||
| chr9:120609862 | A | G | 1 | a0002c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1088-1852T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120609862 | |||||||
| chr9:120610007 | TAAAG | T | 42 | a0001c0002t0001g0189 a0001c0002t0012g0285 a0001c0002t0012g0286 others(39): Show |
43 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1088-2001_1088-199 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120610007 | |||||||
| chr9:120610116 | G | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1088-2106C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120610116 | |||||||
| chr9:120610770 | G | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1087+1626C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120610770 | |||||||
| chr9:120611076 | T | C | 1 | a0001c0003t0003g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1087+1320A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611076 | |||||||
| chr9:120611147 | G | A | 2 | a0001c0003t0005g0160 a0001c0003t0005g0161 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1087+1249C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611147 | |||||||
| chr9:120611278 | T | C | 3 | a0002c0001t0001g0063 a0002c0001t0001g0128 a0002c0001t0001g0129 |
3 | HG02559.hp1 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1087+1118A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611278 | |||||||
| chr9:120611379 | T | C | 1 | a0001c0002t0002g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1087+1017A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611379 | |||||||
| chr9:120611400 | A | G | 5 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1087+996T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611400 | |||||||
| chr9:120611452 | G | C | 1 | a0001c0002t0002g0264 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1087+944C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611452 | |||||||
| chr9:120611716 | A | T | 3 | a0002c0001t0009g0099 a0002c0001t0009g0100 a0002c0001t0009g0101 |
3 | HG01109.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1087+680T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611716 | |||||||
| chr9:120611808 | G | GA | 10 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1087+587dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611808 | |||||||
| chr9:120611808 | G | GAAAGA | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1087+583_1087+587d others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611808 | |||||||
| chr9:120611823 | A | AAAG | 5 | a0001c0003t0003g0143 a0001c0003t0003g0144 a0001c0003t0003g0145 others(2): Show |
5 | HG02451.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1087+572_1087+573i others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611823 | |||||||
| chr9:120611824 | A | AAGAAAGG | 4 | a0001c0003t0003g0141 a0001c0003t0003g0142 a0001c0003t0003g0159 others(1): Show |
4 | HG01891.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087+571_1087+572i others(9): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611824 | |||||||
| chr9:120611824 | A | AAGAAAGG others(4): Show |
1 | a0001c0003t0003g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1087+571_1087+572i others(13): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611824 | |||||||
| chr9:120611828 | A | G | 10 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1087+568T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611828 | |||||||
| chr9:120611832 | A | AAAGG | 41 | a0001c0002t0001g0171 a0002c0001t0001g0002 a0002c0001t0001g0003 others(38): Show |
41 | HG00408.hp2 HG00673.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.1087+560_1087+563d others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611832 | |||||||
| chr9:120611832 | A | AAAGGAAG others(9): Show |
4 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0153 others(1): Show |
4 | HG03098.hp1 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087+548_1087+563d others(18): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611832 | |||||||
| chr9:120611832 | A | AAAGGAAG others(13): Show |
1 | a0001c0003t0008g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1087+544_1087+563d others(22): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611832 | |||||||
| chr9:120611832 | A | AAAGGAAG others(17): Show |
1 | a0001c0003t0011g0156 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1087+540_1087+563d others(26): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611832 | |||||||
| chr9:120611832 | A | AAAGGAAG others(25): Show |
1 | a0001c0003t0011g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1087+563_1087+564i others(34): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611832 | |||||||
| chr9:120611832 | A | G | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1087+564T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611832 | |||||||
| chr9:120611860 | G | A | 4 | a0001c0002t0002g0182 a0001c0002t0002g0217 a0001c0002t0002g0268 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087+536C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611860 | |||||||
| chr9:120611860 | G | GAAGGAAG others(1): Show |
7 | a0001c0002t0002g0216 a0001c0002t0021g0238 a0001c0004t0005g0165 others(4): Show |
7 | HG01081.hp2 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+535_1087+536i others(10): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611860 | |||||||
| chr9:120611860 | G | GAAGGAAG others(9): Show |
2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1087+535_1087+536i others(18): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611860 | |||||||
| chr9:120611861 | A | AAGGAAGA others(3): Show |
2 | a0001c0003t0005g0160 a0001c0003t0005g0161 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1087+534_1087+535i others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611861 | |||||||
| chr9:120611861 | A | AAGGAAGA others(5): Show |
1 | a0001c0002t0002g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1087+534_1087+535i others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611861 | |||||||
| chr9:120611863 | G | GGGAGGAA others(11): Show |
1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1087+532_1087+533i others(20): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611863 | |||||||
| chr9:120611864 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1087+532T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611864 | |||||||
| chr9:120611865 | A | AAGAG | 107 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(104): Show |
107 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1087+527_1087+530d others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611865 | |||||||
| chr9:120611865 | A | G | 21 | a0001c0002t0002g0182 a0001c0002t0002g0203 a0001c0002t0002g0216 others(18): Show |
21 | HG00408.hp1 HG00639.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1087+531T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611865 | |||||||
| chr9:120611865 | AAG | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1087+529_1087+530d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611865 | |||||||
| chr9:120611866 | A | AGG | 7 | a0001c0003t0003g0140 a0001c0003t0003g0143 a0001c0003t0003g0144 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+529_1087+530i others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611866 | |||||||
| chr9:120611883 | G | A | 1 | a0002c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1087+513C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611883 | |||||||
| chr9:120611883 | G | GAGAA | 7 | a0002c0001t0001g0043 a0002c0001t0001g0065 a0002c0001t0001g0074 others(4): Show |
7 | HG01099.hp1 HG01099.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087+509_1087+512d others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611883 | |||||||
| chr9:120611887 | A | G | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1087+509T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611887 | |||||||
| chr9:120611891 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1087+505T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611891 | |||||||
| chr9:120611907 | A | G | 8 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(5): Show |
8 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1087+489T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120611907 | |||||||
| chr9:120612112 | G | A | 8 | a0001c0002t0002g0174 a0001c0002t0002g0175 a0001c0002t0002g0176 others(5): Show |
8 | HG00597.hp1 HG00673.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1087+284C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120612112 | |||||||
| chr9:120612192 | T | C | 1 | a0001c0002t0002g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1087+204A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120612192 | |||||||
| chr9:120612226 | T | A | 8 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(5): Show |
8 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1087+170A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120612226 | |||||||
| chr9:120612361 | T | C | 116 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1087+35A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 4/5 | chr9 | 120612361 | |||||||
| chr9:120612581 | T | C | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.944-42A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120612581 | |||||||
| chr9:120612686 | C | G | 1 | a0002c0001t0001g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.944-147G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120612686 | |||||||
| chr9:120612718 | A | G | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.944-179T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120612718 | |||||||
| chr9:120612832 | C | T | 147 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(144): Show |
147 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.944-293G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120612832 | |||||||
| chr9:120612851 | T | C | 1 | a0002c0001t0001g0023 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.944-312A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120612851 | |||||||
| chr9:120612925 | C | CT | 10 | a0002c0001t0001g0084 a0002c0001t0001g0111 a0002c0001t0004g0079 others(7): Show |
10 | HG00609.hp1 HG02132.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.944-387dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120612925 | |||||||
| chr9:120612925 | CT | C | 25 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.944-387delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120612925 | |||||||
| chr9:120612925 | CTT | C | 118 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(115): Show |
118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.944-388_944-387del others(2): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120612925 | |||||||
| chr9:120613074 | T | C | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.944-535A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613074 | |||||||
| chr9:120613100 | G | A | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.944-561C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613100 | |||||||
| chr9:120613115 | G | A | 1 | a0002c0001t0001g0109 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.944-576C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613115 | |||||||
| chr9:120613160 | T | G | 2 | a0001c0003t0005g0160 a0001c0003t0005g0161 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.944-621A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613160 | |||||||
| chr9:120613249 | T | C | 1 | a0001c0002t0002g0274 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.944-710A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613249 | |||||||
| chr9:120613273 | T | C | 8 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(5): Show |
8 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.944-734A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613273 | |||||||
| chr9:120613309 | T | C | 1 | a0001c0002t0002g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.944-770A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613309 | |||||||
| chr9:120613311 | C | T | 125 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(122): Show |
125 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.944-772G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613311 | |||||||
| chr9:120613376 | C | G | 24 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(21): Show |
24 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.944-837G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613376 | |||||||
| chr9:120613376 | C | T | 1 | a0002c0001t0001g0020 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.944-837G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613376 | |||||||
| chr9:120613431 | A | G | 1 | a0001c0002t0002g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.944-892T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613431 | |||||||
| chr9:120613544 | T | C | 21 | a0001c0002t0002g0164 a0001c0002t0002g0184 a0001c0002t0002g0194 others(18): Show |
21 | HG00639.hp2 HG00735.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.944-1005A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613544 | |||||||
| chr9:120613616 | G | A | 2 | a0001c0003t0003g0141 a0001c0003t0003g0142 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.944-1077C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613616 | |||||||
| chr9:120613948 | A | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.944-1409T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120613948 | |||||||
| chr9:120614017 | AT | A | 131 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(128): Show |
131 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.944-1479delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614017 | |||||||
| chr9:120614143 | C | G | 9 | a0001c0002t0015g0288 a0001c0002t0015g0289 a0001c0003t0008g0150 others(6): Show |
9 | HG01243.hp2 HG02809.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.944-1604G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614143 | |||||||
| chr9:120614180 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.944-1641G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614180 | |||||||
| chr9:120614243 | G | A | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.944-1704C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614243 | |||||||
| chr9:120614331 | C | T | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.944-1792G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614331 | |||||||
| chr9:120614425 | T | C | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.944-1886A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614425 | |||||||
| chr9:120614456 | C | T | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.944-1917G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614456 | |||||||
| chr9:120614489 | A | C | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.944-1950T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614489 | |||||||
| chr9:120614766 | T | G | 1 | a0002c0001t0001g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.944-2227A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614766 | |||||||
| chr9:120614922 | T | C | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.944-2383A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614922 | |||||||
| chr9:120614949 | A | G | 3 | a0001c0003t0003g0159 a0001c0003t0017g0149 a0001c0003t0027g0158 |
3 | HG02809.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.944-2410T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120614949 | |||||||
| chr9:120615086 | A | G | 1 | a0002c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.944-2547T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120615086 | |||||||
| chr9:120615283 | GTGTGCA | G | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.944-2750_944-2745d others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120615283 | |||||||
| chr9:120615315 | G | GCA | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.944-2778_944-2777d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120615315 | |||||||
| chr9:120615328 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.944-2789G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120615328 | |||||||
| chr9:120615598 | A | G | 1 | a0001c0002t0002g0259 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.944-3059T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120615598 | |||||||
| chr9:120615723 | T | C | 1 | a0002c0001t0022g0070 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.944-3184A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120615723 | |||||||
| chr9:120615757 | C | T | 1 | a0002c0001t0007g0088 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.944-3218G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120615757 | |||||||
| chr9:120615844 | T | C | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.944-3305A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120615844 | |||||||
| chr9:120616063 | G | A | 1 | a0002c0001t0009g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.944-3524C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616063 | |||||||
| chr9:120616079 | C | T | 5 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.944-3540G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616079 | |||||||
| chr9:120616146 | ATTACC | A | 4 | a0001c0002t0002g0260 a0001c0002t0002g0261 a0001c0002t0002g0262 others(1): Show |
4 | HG02293.hp2 NA19003.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.944-3612_944-3608d others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616146 | |||||||
| chr9:120616150 | C | T | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.944-3611G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616150 | |||||||
| chr9:120616568 | A | C | 2 | a0001c0003t0017g0149 a0001c0003t0027g0158 |
2 | HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.944-4029T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616568 | |||||||
| chr9:120616571 | C | T | 1 | a0001c0002t0002g0173 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.944-4032G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616571 | |||||||
| chr9:120616677 | C | CA | 8 | a0002c0001t0001g0014 a0002c0001t0001g0019 a0002c0001t0001g0022 others(5): Show |
8 | HG02055.hp2 HG03704.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.944-4139dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616677 | |||||||
| chr9:120616677 | CA | C | 40 | a0001c0002t0001g0189 a0001c0002t0002g0180 a0001c0002t0012g0287 others(37): Show |
41 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.944-4139delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616677 | |||||||
| chr9:120616677 | CAA | C | 17 | a0001c0002t0002g0192 a0001c0002t0002g0193 a0001c0002t0002g0196 others(14): Show |
17 | HG00738.hp1 HG01192.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.944-4140_944-4139d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616677 | |||||||
| chr9:120616677 | CAAA | C | 106 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(103): Show |
106 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.944-4141_944-4139d others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616677 | |||||||
| chr9:120616677 | CAAAA | C | 10 | a0001c0002t0002g0220 a0001c0002t0002g0263 a0001c0002t0006g0271 others(7): Show |
10 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.944-4142_944-4139d others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616677 | |||||||
| chr9:120616677 | CAAAAAA | C | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.944-4144_944-4139d others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616677 | |||||||
| chr9:120616876 | A | G | 3 | a0001c0002t0002g0193 a0001c0002t0002g0198 a0001c0002t0002g0217 |
3 | HG01106.hp1 HG01192.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.944-4337T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120616876 | |||||||
| chr9:120617011 | T | TAAAAATA others(325): Show |
1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.944-4473_944-4472i others(334): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120617011 | |||||||
| chr9:120617304 | T | C | 1 | a0002c0001t0007g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.944-4765A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120617304 | |||||||
| chr9:120617948 | A | G | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.943+4668T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120617948 | |||||||
| chr9:120618010 | T | C | 1 | a0001c0002t0002g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.943+4606A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618010 | |||||||
| chr9:120618065 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.943+4551G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618065 | |||||||
| chr9:120618330 | T | C | 1 | a0001c0002t0002g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.943+4286A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618330 | |||||||
| chr9:120618668 | T | C | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.943+3948A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618668 | |||||||
| chr9:120618773 | G | A | 1 | a0002c0001t0001g0119 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.943+3843C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618773 | |||||||
| chr9:120618815 | G | C | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.943+3801C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618815 | |||||||
| chr9:120618854 | C | G | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.943+3762G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618854 | |||||||
| chr9:120618855 | G | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.943+3761C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618855 | |||||||
| chr9:120618897 | CA | C | 8 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(5): Show |
8 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.943+3718delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618897 | |||||||
| chr9:120618944 | C | T | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.943+3672G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120618944 | |||||||
| chr9:120619204 | G | A | 1 | a0002c0001t0001g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.943+3412C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120619204 | |||||||
| chr9:120619332 | G | A | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.943+3284C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120619332 | |||||||
| chr9:120619500 | A | G | 2 | a0002c0001t0007g0091 a0002c0001t0007g0092 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.943+3116T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120619500 | |||||||
| chr9:120619684 | T | C | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.943+2932A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120619684 | |||||||
| chr9:120619853 | C | T | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.943+2763G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120619853 | |||||||
| chr9:120619894 | G | T | 1 | a0001c0002t0014g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.943+2722C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120619894 | |||||||
| chr9:120619964 | TAA | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+2650_943+2651d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120619964 | |||||||
| chr9:120620343 | C | T | 2 | a0001c0003t0003g0159 a0001c0003t0027g0158 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.943+2273G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120620343 | |||||||
| chr9:120620658 | G | A | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.943+1958C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120620658 | |||||||
| chr9:120620681 | G | T | 2 | a0002c0001t0007g0091 a0002c0001t0007g0092 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.943+1935C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120620681 | |||||||
| chr9:120620699 | T | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.943+1917A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120620699 | |||||||
| chr9:120620854 | G | GA | 147 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(144): Show |
147 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.943+1761dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120620854 | |||||||
| chr9:120620915 | TA | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.943+1700delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120620915 | |||||||
| chr9:120620929 | G | A | 2 | a0002c0001t0002g0066 a0002c0001t0002g0067 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.943+1687C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120620929 | |||||||
| chr9:120621306 | T | C | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.943+1310A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621306 | |||||||
| chr9:120621352 | T | C | 151 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(148): Show |
151 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.943+1264A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621352 | |||||||
| chr9:120621368 | G | A | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.943+1248C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621368 | |||||||
| chr9:120621460 | A | G | 2 | a0001c0003t0003g0159 a0001c0003t0027g0158 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.943+1156T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621460 | |||||||
| chr9:120621513 | A | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.943+1103T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621513 | |||||||
| chr9:120621631 | C | T | 87 | a0001c0002t0002g0170 a0001c0002t0002g0172 a0001c0002t0002g0173 others(84): Show |
87 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.943+985G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621631 | |||||||
| chr9:120621673 | C | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.943+943G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621673 | |||||||
| chr9:120621828 | C | T | 1 | a0001c0002t0002g0256 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.943+788G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621828 | |||||||
| chr9:120621895 | C | CATGACCC others(17): Show |
16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.943+720_943+721ins others(24): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621895 | |||||||
| chr9:120621938 | G | A | 1 | a0001c0002t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.943+678C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621938 | |||||||
| chr9:120621993 | T | G | 3 | a0002c0001t0004g0011 a0002c0001t0004g0079 a0002c0001t0004g0080 |
3 | NA18964.hp2 NA19062.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.943+623A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120621993 | |||||||
| chr9:120622124 | C | T | 1 | a0002c0001t0001g0051 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.943+492G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622124 | |||||||
| chr9:120622202 | T | C | 1 | a0001c0003t0011g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.943+414A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622202 | |||||||
| chr9:120622417 | C | CTTTTTTT | 12 | a0001c0002t0002g0174 a0001c0002t0002g0183 a0001c0002t0002g0191 others(9): Show |
12 | HG00323.hp2 HG00558.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+192_943+198dup others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622417 | |||||||
| chr9:120622417 | C | CTTTTTTT others(1): Show |
99 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(96): Show |
99 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.943+191_943+198dup others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622417 | |||||||
| chr9:120622417 | C | CTTTTTTT others(2): Show |
12 | a0001c0002t0002g0211 a0001c0002t0002g0261 a0001c0002t0015g0288 others(9): Show |
12 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.943+190_943+198dup others(9): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622417 | |||||||
| chr9:120622417 | C | T | 7 | a0002c0001t0001g0041 a0002c0001t0001g0043 a0002c0001t0001g0065 others(4): Show |
7 | HG02293.hp1 HG02735.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.943+199G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622417 | |||||||
| chr9:120622434 | T | TTTTTTTT others(4): Show |
1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.943+181_943+182ins others(11): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622434 | |||||||
| chr9:120622442 | G | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.943+174C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622442 | |||||||
| chr9:120622471 | T | C | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.943+145A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622471 | |||||||
| chr9:120622510 | A | G | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.943+106T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 3/5 | chr9 | 120622510 | |||||||
| chr9:120623190 | C | T | 1 | a0001c0010t0005g0169 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.804-435G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120623190 | |||||||
| chr9:120623259 | C | CAAATAAC others(316): Show |
2 | a0001c0003t0003g0159 a0001c0003t0027g0158 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.804-505_804-504ins others(323): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120623259 | |||||||
| chr9:120623578 | T | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-823A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120623578 | |||||||
| chr9:120623589 | A | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-834T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120623589 | |||||||
| chr9:120623615 | G | A | 1 | a0002c0001t0001g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.804-860C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120623615 | |||||||
| chr9:120623702 | T | C | 5 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-947A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120623702 | |||||||
| chr9:120623758 | C | G | 8 | a0001c0002t0015g0288 a0001c0002t0015g0289 a0001c0003t0008g0150 others(5): Show |
8 | HG01243.hp2 HG02809.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.804-1003G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120623758 | |||||||
| chr9:120623915 | A | G | 1 | a0002c0001t0009g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.804-1160T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120623915 | |||||||
| chr9:120624223 | G | A | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-1468C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624223 | |||||||
| chr9:120624376 | C | T | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-1621G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624376 | |||||||
| chr9:120624384 | C | T | 1 | a0002c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.804-1629G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624384 | |||||||
| chr9:120624508 | A | G | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-1753T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624508 | |||||||
| chr9:120624572 | T | G | 1 | a0002c0001t0001g0078 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.804-1817A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624572 | |||||||
| chr9:120624588 | C | T | 1 | a0001c0002t0002g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.804-1833G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624588 | |||||||
| chr9:120624594 | G | A | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-1839C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624594 | |||||||
| chr9:120624655 | T | A | 1 | a0001c0002t0002g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.804-1900A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624655 | |||||||
| chr9:120624679 | G | A | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-1924C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624679 | |||||||
| chr9:120624688 | A | G | 3 | a0001c0003t0008g0151 a0001c0003t0008g0152 a0001c0003t0008g0153 |
3 | HG03041.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.804-1933T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624688 | |||||||
| chr9:120624798 | A | G | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-2043T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624798 | |||||||
| chr9:120624872 | CA | C | 120 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(117): Show |
120 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.804-2118delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624872 | |||||||
| chr9:120624872 | CAA | C | 24 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(21): Show |
24 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.804-2119_804-2118d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120624872 | |||||||
| chr9:120625427 | T | TG | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-2673dupC | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625427 | |||||||
| chr9:120625438 | G | A | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-2683C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625438 | |||||||
| chr9:120625519 | G | A | 1 | a0001c0002t0023g0240 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.804-2764C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625519 | |||||||
| chr9:120625535 | TA | T | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-2781delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625535 | |||||||
| chr9:120625617 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.804-2862G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625617 | |||||||
| chr9:120625662 | C | T | 3 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0179 |
3 | HG00597.hp1 NA19004.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.804-2907G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625662 | |||||||
| chr9:120625689 | C | T | 1 | a0001c0002t0002g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.804-2934G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625689 | |||||||
| chr9:120625735 | G | C | 1 | a0001c0002t0002g0269 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804-2980C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625735 | |||||||
| chr9:120625807 | C | A | 1 | a0001c0003t0005g0160 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.804-3052G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625807 | |||||||
| chr9:120625807 | C | G | 3 | a0001c0003t0005g0161 a0001c0003t0005g0162 a0001c0003t0018g0157 |
3 | HG00639.hp1 HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.804-3052G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625807 | |||||||
| chr9:120625833 | C | CA | 13 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(10): Show |
13 | HG01169.hp2 HG01358.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.804-3079dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625833 | |||||||
| chr9:120625833 | CA | C | 48 | a0001c0002t0001g0189 a0001c0003t0008g0150 a0001c0003t0008g0151 others(45): Show |
49 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.804-3079delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625833 | |||||||
| chr9:120625849 | A | AAAAG | 105 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(102): Show |
105 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.804-3095_804-3094i others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625849 | |||||||
| chr9:120625849 | A | G | 1 | a0001c0003t0005g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.804-3094T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625849 | |||||||
| chr9:120625853 | A | AAG | 10 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.804-3099_804-3098i others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625853 | |||||||
| chr9:120625853 | A | AG | 3 | a0001c0003t0017g0149 a0001c0003t0018g0157 a0001c0003t0027g0158 |
3 | HG00639.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.804-3099_804-3098i others(3): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625853 | |||||||
| chr9:120625853 | A | AGAAAG | 8 | a0001c0002t0002g0192 a0001c0002t0002g0207 a0001c0002t0002g0242 others(5): Show |
8 | HG01981.hp2 HG02074.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.804-3099_804-3098i others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625853 | |||||||
| chr9:120625853 | A | G | 129 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.804-3098T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625853 | |||||||
| chr9:120625890 | T | C | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-3135A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120625890 | |||||||
| chr9:120626029 | G | A | 1 | a0002c0001t0001g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.804-3274C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626029 | |||||||
| chr9:120626055 | T | C | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-3300A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626055 | |||||||
| chr9:120626112 | G | A | 1 | a0002c0001t0001g0014 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.804-3357C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626112 | |||||||
| chr9:120626115 | T | G | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.804-3360A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626115 | |||||||
| chr9:120626186 | C | T | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.804-3431G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626186 | |||||||
| chr9:120626245 | C | G | 1 | a0001c0002t0002g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.804-3490G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626245 | |||||||
| chr9:120626400 | C | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-3645G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626400 | |||||||
| chr9:120626683 | T | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.804-3928A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626683 | |||||||
| chr9:120626724 | G | A | 1 | a0002c0001t0001g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.804-3969C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626724 | |||||||
| chr9:120626741 | T | C | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-3986A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626741 | |||||||
| chr9:120626926 | G | A | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.804-4171C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120626926 | |||||||
| chr9:120627195 | T | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-4440A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627195 | |||||||
| chr9:120627310 | T | C | 1 | a0001c0002t0002g0194 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.804-4555A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627310 | |||||||
| chr9:120627407 | T | C | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-4652A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627407 | |||||||
| chr9:120627421 | C | G | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-4666G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627421 | |||||||
| chr9:120627555 | T | C | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-4800A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627555 | |||||||
| chr9:120627565 | C | T | 1 | a0001c0003t0003g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.804-4810G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627565 | |||||||
| chr9:120627616 | T | C | 1 | a0002c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.804-4861A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627616 | |||||||
| chr9:120627619 | C | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.804-4864G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627619 | |||||||
| chr9:120627736 | T | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-4981A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627736 | |||||||
| chr9:120627894 | G | T | 3 | a0002c0001t0010g0053 a0002c0001t0010g0094 a0002c0001t0010g0095 |
3 | HG01099.hp2 HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.804-5139C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627894 | |||||||
| chr9:120627899 | T | C | 2 | a0002c0001t0001g0071 a0002c0001t0001g0072 |
2 | HG00438.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.804-5144A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120627899 | |||||||
| chr9:120628021 | A | G | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804-5266T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628021 | |||||||
| chr9:120628080 | G | A | 11 | a0001c0002t0002g0186 a0001c0002t0002g0187 a0001c0002t0002g0228 others(8): Show |
11 | HG00558.hp1 HG00621.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-5325C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628080 | |||||||
| chr9:120628118 | C | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.804-5363G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628118 | |||||||
| chr9:120628211 | T | C | 2 | a0001c0002t0002g0250 a0001c0002t0002g0253 |
2 | HG00558.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.804-5456A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628211 | |||||||
| chr9:120628371 | T | C | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-5616A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628371 | |||||||
| chr9:120628467 | TG | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-5713delC | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628467 | |||||||
| chr9:120628468 | G | GT | 41 | a0001c0002t0001g0171 a0001c0002t0002g0183 a0001c0002t0002g0186 others(38): Show |
41 | HG00642.hp2 HG00673.hp1 HG01975.hp1 others(38): Show |
intron_variant | MODIFIER | c.804-5714dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628468 | |||||||
| chr9:120628468 | G | GTT | 114 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(111): Show |
114 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.804-5715_804-5714d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628468 | |||||||
| chr9:120628468 | G | GTTT | 18 | a0001c0002t0001g0189 a0001c0002t0002g0173 a0001c0002t0002g0190 others(15): Show |
18 | HG00408.hp1 HG00438.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.804-5716_804-5714d others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628468 | |||||||
| chr9:120628468 | G | T | 1 | a0001c0002t0002g0230 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.804-5713C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628468 | |||||||
| chr9:120628468 | GT | G | 9 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0008g0150 others(6): Show |
9 | HG02572.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-5714delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628468 | |||||||
| chr9:120628495 | T | C | 2 | a0001c0002t0015g0288 a0001c0003t0017g0149 |
2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.804-5740A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628495 | |||||||
| chr9:120628683 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.804-5928C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628683 | |||||||
| chr9:120628715 | G | A | 1 | a0002c0001t0001g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.804-5960C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628715 | |||||||
| chr9:120628819 | G | A | 1 | a0002c0001t0002g0131 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.804-6064C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628819 | |||||||
| chr9:120628824 | A | T | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-6069T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628824 | |||||||
| chr9:120628834 | A | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.804-6079T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628834 | |||||||
| chr9:120628980 | G | GT | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-6226dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120628980 | |||||||
| chr9:120629030 | C | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-6275G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629030 | |||||||
| chr9:120629175 | A | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-6420T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629175 | |||||||
| chr9:120629325 | G | A | 2 | a0002c0001t0001g0023 a0002c0001t0001g0137 |
2 | HG00408.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.804-6570C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629325 | |||||||
| chr9:120629415 | A | G | 15 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(12): Show |
15 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-6660T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629415 | |||||||
| chr9:120629445 | G | C | 8 | a0001c0002t0002g0174 a0001c0002t0002g0175 a0001c0002t0002g0176 others(5): Show |
8 | HG00597.hp1 HG00673.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.804-6690C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629445 | |||||||
| chr9:120629539 | G | A | 2 | a0002c0001t0002g0066 a0002c0001t0002g0067 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.804-6784C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629539 | |||||||
| chr9:120629569 | C | T | 43 | a0001c0002t0001g0171 a0002c0001t0001g0002 a0002c0001t0001g0003 others(40): Show |
43 | HG00408.hp2 HG00673.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.804-6814G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629569 | |||||||
| chr9:120629723 | C | G | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804-6968G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629723 | |||||||
| chr9:120629762 | G | A | 1 | a0002c0001t0001g0130 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.804-7007C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629762 | |||||||
| chr9:120629843 | G | A | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.804-7088C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629843 | |||||||
| chr9:120629870 | T | G | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804-7115A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629870 | |||||||
| chr9:120629914 | C | T | 1 | a0003c0007t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.804-7159G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629914 | |||||||
| chr9:120629932 | CA | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-7178delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120629932 | |||||||
| chr9:120630078 | C | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-7323G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630078 | |||||||
| chr9:120630152 | A | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.804-7397T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630152 | |||||||
| chr9:120630200 | C | T | 17 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(14): Show |
17 | HG00408.hp2 HG02040.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.804-7445G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630200 | |||||||
| chr9:120630209 | C | A | 5 | a0002c0001t0001g0014 a0002c0001t0001g0019 a0002c0001t0001g0027 others(2): Show |
5 | NA18966.hp2 NA18975.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-7454G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630209 | |||||||
| chr9:120630430 | G | T | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804-7675C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630430 | |||||||
| chr9:120630470 | T | C | 118 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(115): Show |
118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.804-7715A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630470 | |||||||
| chr9:120630519 | T | C | 8 | a0001c0002t0002g0235 a0001c0002t0002g0277 a0001c0002t0002g0278 others(5): Show |
8 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.804-7764A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630519 | |||||||
| chr9:120630559 | A | G | 1 | a0002c0001t0001g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.804-7804T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630559 | |||||||
| chr9:120630729 | G | T | 6 | a0001c0002t0002g0214 a0001c0002t0002g0224 a0001c0002t0002g0225 others(3): Show |
6 | HG00639.hp2 HG00735.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.804-7974C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630729 | |||||||
| chr9:120630831 | A | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-8076T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630831 | |||||||
| chr9:120630956 | C | T | 1 | a0002c0001t0001g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.804-8201G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120630956 | |||||||
| chr9:120631071 | C | T | 5 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-8316G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631071 | |||||||
| chr9:120631107 | T | G | 1 | a0002c0001t0001g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.804-8352A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631107 | |||||||
| chr9:120631400 | C | T | 1 | a0002c0001t0001g0028 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.804-8645G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631400 | |||||||
| chr9:120631487 | A | AT | 131 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0173 others(128): Show |
131 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.804-8733dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631487 | |||||||
| chr9:120631487 | A | ATT | 7 | a0001c0002t0002g0172 a0001c0002t0002g0182 a0001c0003t0005g0160 others(4): Show |
7 | HG00639.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.804-8734_804-8733d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631487 | |||||||
| chr9:120631528 | G | A | 1 | a0001c0002t0002g0227 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.804-8773C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631528 | |||||||
| chr9:120631660 | A | T | 276 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0002t0002g0164 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.804-8905T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631660 | |||||||
| chr9:120631767 | A | G | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.804-9012T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631767 | |||||||
| chr9:120631776 | T | C | 1 | a0002c0001t0001g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.804-9021A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120631776 | |||||||
| chr9:120632336 | G | GT | 15 | a0001c0002t0015g0288 a0001c0002t0015g0289 a0002c0001t0001g0033 others(12): Show |
15 | HG01243.hp2 HG01261.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-9582dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632336 | |||||||
| chr9:120632336 | GT | G | 128 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(125): Show |
128 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.804-9582delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632336 | |||||||
| chr9:120632336 | GTT | G | 9 | a0001c0002t0002g0234 a0001c0002t0002g0272 a0001c0002t0002g0273 others(6): Show |
9 | HG02040.hp2 HG02615.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-9583_804-9582d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632336 | |||||||
| chr9:120632336 | GTTT | G | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-9584_804-9582d others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632336 | |||||||
| chr9:120632337 | T | G | 1 | a0002c0001t0001g0031 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.804-9582A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632337 | |||||||
| chr9:120632615 | G | C | 2 | a0001c0003t0003g0159 a0001c0003t0027g0158 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.804-9860C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632615 | |||||||
| chr9:120632616 | C | G | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.804-9861G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632616 | |||||||
| chr9:120632632 | T | C | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-9877A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632632 | |||||||
| chr9:120632798 | G | A | 2 | a0002c0001t0002g0066 a0002c0001t0002g0067 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.804-10043C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120632798 | |||||||
| chr9:120633056 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.804-10301A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120633056 | |||||||
| chr9:120633310 | G | T | 1 | a0002c0001t0001g0025 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.804-10555C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120633310 | |||||||
| chr9:120633474 | G | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-10719C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120633474 | |||||||
| chr9:120634074 | A | G | 3 | a0001c0002t0002g0260 a0001c0002t0002g0261 a0001c0002t0002g0263 |
3 | NA19003.hp1 NA19083.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.804-11319T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634074 | |||||||
| chr9:120634093 | G | A | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-11338C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634093 | |||||||
| chr9:120634314 | C | T | 1 | a0001c0002t0012g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.804-11559G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634314 | |||||||
| chr9:120634438 | TGGAATAT others(128): Show |
T | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-11818_804-1168 others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634438 | |||||||
| chr9:120634446 | C | CT | 20 | a0001c0002t0001g0189 a0002c0001t0001g0010 a0002c0001t0001g0021 others(17): Show |
20 | HG00642.hp2 HG01496.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.804-11692dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634446 | |||||||
| chr9:120634446 | C | CTTTTTTT others(3): Show |
53 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0174 others(50): Show |
53 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.804-11701_804-1169 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634446 | |||||||
| chr9:120634446 | C | CTTTTTTT others(4): Show |
33 | a0001c0002t0002g0173 a0001c0002t0002g0178 a0001c0002t0002g0179 others(30): Show |
33 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.804-11702_804-1169 others(15): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634446 | |||||||
| chr9:120634446 | C | CTTTTTTT others(5): Show |
13 | a0001c0002t0002g0172 a0001c0002t0002g0207 a0001c0002t0002g0212 others(10): Show |
13 | HG01070.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.804-11703_804-1169 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634446 | |||||||
| chr9:120634446 | C | CTTTTTTT others(6): Show |
2 | a0001c0002t0002g0248 a0001c0002t0016g0247 |
2 | HG00621.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.804-11704_804-1169 others(17): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634446 | |||||||
| chr9:120634446 | C | CTTTTTTT others(8): Show |
1 | a0001c0008t0002g0163 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.804-11706_804-1169 others(19): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634446 | |||||||
| chr9:120634446 | CT | C | 6 | a0001c0003t0008g0151 a0001c0003t0008g0152 a0002c0001t0001g0043 others(3): Show |
6 | HG00323.hp1 HG01884.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.804-11692delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634446 | |||||||
| chr9:120634446 | CTTTTTTT others(3): Show |
C | 4 | a0001c0002t0006g0258 a0001c0002t0006g0265 a0001c0002t0006g0266 others(1): Show |
4 | NA18971.hp1 NA18984.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-11701_804-1169 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634446 | |||||||
| chr9:120634514 | G | C | 43 | a0001c0002t0002g0172 a0001c0002t0002g0174 a0001c0002t0002g0175 others(40): Show |
43 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.804-11759C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634514 | |||||||
| chr9:120634523 | T | C | 182 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.804-11768A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634523 | |||||||
| chr9:120634566 | C | T | 1 | a0002c0001t0001g0118 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.804-11811G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634566 | |||||||
| chr9:120634612 | A | G | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.804-11857T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634612 | |||||||
| chr9:120634635 | T | C | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-11880A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634635 | |||||||
| chr9:120634748 | G | A | 1 | a0001c0002t0021g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.804-11993C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634748 | |||||||
| chr9:120634831 | T | C | 1 | a0001c0002t0002g0256 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.804-12076A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634831 | |||||||
| chr9:120634903 | A | T | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-12148T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634903 | |||||||
| chr9:120634967 | T | G | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-12212A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120634967 | |||||||
| chr9:120635298 | T | C | 276 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0002t0002g0164 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.804-12543A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120635298 | |||||||
| chr9:120635366 | C | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.804-12611G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120635366 | |||||||
| chr9:120635525 | T | G | 1 | a0002c0001t0001g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.804-12770A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120635525 | |||||||
| chr9:120635773 | T | TA | 3 | a0001c0003t0017g0149 a0002c0001t0001g0089 a0002c0001t0001g0117 |
3 | HG02809.hp2 HG03139.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.804-13019dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120635773 | |||||||
| chr9:120635867 | A | T | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-13112T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120635867 | |||||||
| chr9:120635884 | T | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.804-13129A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120635884 | |||||||
| chr9:120635898 | G | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-13143C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120635898 | |||||||
| chr9:120636078 | C | T | 1 | a0001c0002t0002g0205 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.804-13323G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636078 | |||||||
| chr9:120636082 | T | C | 1 | a0001c0002t0002g0218 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.804-13327A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636082 | |||||||
| chr9:120636083 | A | G | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-13328T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636083 | |||||||
| chr9:120636135 | G | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-13380C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636135 | |||||||
| chr9:120636228 | G | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-13473C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636228 | |||||||
| chr9:120636357 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.804-13602A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636357 | |||||||
| chr9:120636371 | A | T | 1 | a0002c0001t0025g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.804-13616T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636371 | |||||||
| chr9:120636436 | T | G | 1 | a0002c0001t0001g0007 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.804-13681A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636436 | |||||||
| chr9:120636593 | C | T | 1 | a0002c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.804-13838G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636593 | |||||||
| chr9:120636666 | T | A | 1 | a0001c0002t0002g0275 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.804-13911A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636666 | |||||||
| chr9:120636717 | C | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-13962G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636717 | |||||||
| chr9:120636758 | C | T | 1 | a0001c0002t0006g0271 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.804-14003G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636758 | |||||||
| chr9:120636783 | C | T | 5 | a0001c0002t0001g0171 a0002c0001t0001g0018 a0002c0001t0001g0029 others(2): Show |
5 | HG00673.hp1 NA18967.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.804-14028G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636783 | |||||||
| chr9:120636788 | G | A | 1 | a0002c0001t0001g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.804-14033C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636788 | |||||||
| chr9:120636791 | C | T | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-14036G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636791 | |||||||
| chr9:120636798 | C | T | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-14043G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636798 | |||||||
| chr9:120636829 | G | A | 2 | a0002c0001t0001g0018 a0002c0001t0001g0033 |
2 | NA19006.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.804-14074C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636829 | |||||||
| chr9:120636833 | G | A | 1 | a0001c0002t0002g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.804-14078C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636833 | |||||||
| chr9:120636854 | G | GT | 3 | a0001c0002t0002g0272 a0001c0002t0002g0273 a0001c0002t0002g0274 |
3 | HG02040.hp2 NA18949.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.804-14100dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636854 | |||||||
| chr9:120636855 | T | TG | 83 | a0001c0002t0002g0170 a0001c0002t0002g0172 a0001c0002t0002g0173 others(80): Show |
83 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.804-14101dupC | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636855 | |||||||
| chr9:120636874 | G | A | 2 | a0002c0001t0001g0069 a0002c0001t0001g0105 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.804-14119C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636874 | |||||||
| chr9:120636911 | G | A | 2 | a0002c0001t0001g0048 a0002c0001t0001g0050 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.804-14156C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636911 | |||||||
| chr9:120636918 | A | AC | 23 | a0001c0002t0002g0172 a0001c0002t0002g0179 a0001c0002t0002g0192 others(20): Show |
23 | HG00558.hp1 HG00597.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.804-14164dupG | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120636918 | |||||||
| chr9:120637058 | T | C | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-14303A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637058 | |||||||
| chr9:120637198 | CT | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-14444delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637198 | |||||||
| chr9:120637203 | T | G | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-14448A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637203 | |||||||
| chr9:120637232 | G | C | 1 | a0001c0002t0002g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.804-14477C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637232 | |||||||
| chr9:120637250 | T | A | 1 | a0001c0002t0002g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.804-14495A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637250 | |||||||
| chr9:120637297 | G | A | 1 | a0002c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.804-14542C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637297 | |||||||
| chr9:120637416 | C | A | 1 | a0001c0003t0003g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.804-14661G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637416 | |||||||
| chr9:120637438 | A | T | 1 | a0002c0001t0001g0027 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.804-14683T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637438 | |||||||
| chr9:120637487 | TA | T | 20 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(17): Show |
20 | HG00642.hp2 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.804-14733delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637487 | |||||||
| chr9:120637560 | G | A | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-14805C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637560 | |||||||
| chr9:120637602 | G | T | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-14847C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637602 | |||||||
| chr9:120637746 | G | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-14991C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637746 | |||||||
| chr9:120637790 | C | CA | 56 | a0001c0002t0002g0164 a0001c0002t0002g0184 a0001c0002t0002g0185 others(53): Show |
56 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.804-15036dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | C | CAA | 66 | a0001c0002t0002g0173 a0001c0002t0002g0174 a0001c0002t0002g0177 others(63): Show |
66 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.804-15037_804-1503 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | C | CAAA | 27 | a0001c0002t0002g0170 a0001c0002t0002g0172 a0001c0002t0002g0175 others(24): Show |
27 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.804-15038_804-1503 others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | C | CAAAAAAA | 6 | a0001c0003t0003g0142 a0001c0003t0003g0143 a0001c0003t0003g0144 others(3): Show |
6 | HG02451.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.804-15042_804-1503 others(11): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | C | CAAAAAAA others(3): Show |
2 | a0001c0002t0012g0285 a0001c0002t0012g0286 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.804-15045_804-1503 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | C | CAAAAAAA others(4): Show |
1 | a0001c0004t0005g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.804-15046_804-1503 others(15): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | C | CAAAAAAA others(5): Show |
1 | a0001c0004t0005g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.804-15047_804-1503 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | CA | C | 9 | a0001c0003t0003g0159 a0002c0001t0001g0024 a0002c0001t0001g0054 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-15036delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0012g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.804-15045_804-1503 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637790 | CAAAAAAA others(5): Show |
C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-15047_804-1503 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637790 | |||||||
| chr9:120637876 | A | G | 1 | a0002c0001t0001g0025 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.804-15121T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120637876 | |||||||
| chr9:120638137 | G | A | 2 | a0001c0004t0005g0165 a0001c0004t0005g0166 |
2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.804-15382C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638137 | |||||||
| chr9:120638143 | G | A | 8 | a0002c0001t0001g0015 a0002c0001t0001g0042 a0002c0001t0001g0046 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.804-15388C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638143 | |||||||
| chr9:120638153 | G | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-15398C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638153 | |||||||
| chr9:120638215 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-15460G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638215 | |||||||
| chr9:120638219 | C | T | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-15464G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638219 | |||||||
| chr9:120638277 | C | T | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-15522G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638277 | |||||||
| chr9:120638433 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.804-15678G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638433 | |||||||
| chr9:120638620 | G | A | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.804-15865C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638620 | |||||||
| chr9:120638696 | C | G | 151 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(148): Show |
151 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.804-15941G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638696 | |||||||
| chr9:120638808 | T | G | 1 | a0002c0001t0001g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.804-16053A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638808 | |||||||
| chr9:120638916 | G | A | 1 | a0001c0002t0002g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.804-16161C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638916 | |||||||
| chr9:120638972 | T | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.804-16217A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120638972 | |||||||
| chr9:120639180 | T | C | 1 | a0001c0003t0003g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804-16425A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639180 | |||||||
| chr9:120639222 | AC | A | 8 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.804-16468delG | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639222 | |||||||
| chr9:120639342 | C | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.804-16587G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639342 | |||||||
| chr9:120639476 | C | A | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-16721G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639476 | |||||||
| chr9:120639479 | G | A | 1 | a0001c0002t0002g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.804-16724C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639479 | |||||||
| chr9:120639502 | C | T | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-16747G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639502 | |||||||
| chr9:120639508 | T | TA | 12 | a0001c0002t0002g0173 a0001c0002t0002g0196 a0001c0002t0002g0200 others(9): Show |
12 | HG00642.hp2 HG00735.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.804-16754dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639508 | |||||||
| chr9:120639508 | TA | T | 23 | a0001c0002t0002g0176 a0001c0002t0002g0221 a0001c0002t0002g0223 others(20): Show |
23 | HG00323.hp2 HG00558.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.804-16754delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639508 | |||||||
| chr9:120639508 | TAAAAAAA others(5): Show |
T | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-16765_804-1675 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639508 | |||||||
| chr9:120639668 | A | G | 1 | a0001c0003t0011g0154 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.804-16913T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639668 | |||||||
| chr9:120639795 | A | ATTAAG | 138 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(135): Show |
138 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.804-17041_804-1704 others(9): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639795 | |||||||
| chr9:120639934 | C | G | 11 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(8): Show |
11 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.804-17179G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120639934 | |||||||
| chr9:120640053 | T | C | 3 | a0002c0001t0010g0053 a0002c0001t0010g0094 a0002c0001t0010g0095 |
3 | HG01099.hp2 HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.804-17298A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120640053 | |||||||
| chr9:120640082 | A | C | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG00639.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-17327T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120640082 | |||||||
| chr9:120640598 | CTATGTGT others(11): Show |
C | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804-17861_804-1784 others(22): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120640598 | |||||||
| chr9:120640639 | G | A | 1 | a0001c0003t0003g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804-17884C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120640639 | |||||||
| chr9:120640988 | C | T | 1 | a0002c0006t0001g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.804-18233G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120640988 | |||||||
| chr9:120641047 | T | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-18292A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641047 | |||||||
| chr9:120641083 | C | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+18291G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641083 | |||||||
| chr9:120641132 | A | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+18242T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641132 | |||||||
| chr9:120641133 | T | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+18241A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641133 | |||||||
| chr9:120641178 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803+18196A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641178 | |||||||
| chr9:120641521 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+17853G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641521 | |||||||
| chr9:120641644 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803+17730A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641644 | |||||||
| chr9:120641712 | G | A | 37 | a0001c0002t0001g0171 a0002c0001t0001g0002 a0002c0001t0001g0003 others(34): Show |
37 | HG00408.hp2 HG00673.hp1 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.803+17662C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641712 | |||||||
| chr9:120641934 | T | C | 1 | a0001c0002t0002g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.803+17440A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120641934 | |||||||
| chr9:120642097 | T | C | 2 | a0001c0002t0002g0251 a0001c0002t0002g0252 |
2 | NA19010.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.803+17277A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120642097 | |||||||
| chr9:120642110 | A | G | 1 | a0002c0001t0001g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.803+17264T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120642110 | |||||||
| chr9:120642125 | C | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+17249G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120642125 | |||||||
| chr9:120642230 | C | T | 37 | a0001c0002t0001g0171 a0002c0001t0001g0002 a0002c0001t0001g0003 others(34): Show |
37 | HG00408.hp2 HG00673.hp1 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.803+17144G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120642230 | |||||||
| chr9:120642332 | T | C | 118 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(115): Show |
119 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.803+17042A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120642332 | |||||||
| chr9:120642560 | T | C | 1 | a0002c0001t0001g0007 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.803+16814A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120642560 | |||||||
| chr9:120642690 | A | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.803+16684T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120642690 | |||||||
| chr9:120642766 | T | G | 1 | a0001c0002t0002g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.803+16608A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120642766 | |||||||
| chr9:120643001 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+16373T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643001 | |||||||
| chr9:120643067 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803+16307A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643067 | |||||||
| chr9:120643226 | GA | G | 7 | a0001c0002t0002g0182 a0001c0002t0012g0285 a0001c0002t0012g0286 others(4): Show |
7 | HG02572.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+16147delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643226 | |||||||
| chr9:120643226 | GAA | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+16146_803+1614 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643226 | |||||||
| chr9:120643329 | A | G | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.803+16045T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643329 | |||||||
| chr9:120643526 | TAAGGACC | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+15841_803+1584 others(11): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643526 | |||||||
| chr9:120643536 | C | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+15838G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643536 | |||||||
| chr9:120643547 | A | C | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803+15827T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643547 | |||||||
| chr9:120643622 | A | G | 5 | a0001c0002t0002g0172 a0001c0002t0002g0200 a0001c0002t0002g0201 others(2): Show |
5 | HG03654.hp1 NA18966.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+15752T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643622 | |||||||
| chr9:120643804 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803+15570G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643804 | |||||||
| chr9:120643907 | G | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+15467C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120643907 | |||||||
| chr9:120644071 | A | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.803+15303T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644071 | |||||||
| chr9:120644173 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+15201C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644173 | |||||||
| chr9:120644188 | C | G | 1 | a0001c0002t0002g0278 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.803+15186G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644188 | |||||||
| chr9:120644524 | C | T | 1 | a0001c0002t0012g0285 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.803+14850G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644524 | |||||||
| chr9:120644525 | G | A | 3 | a0001c0003t0011g0154 a0001c0003t0011g0155 a0001c0003t0011g0156 |
3 | HG02809.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.803+14849C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644525 | |||||||
| chr9:120644635 | G | A | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803+14739C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644635 | |||||||
| chr9:120644741 | C | T | 1 | a0002c0001t0001g0012 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.803+14633G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644741 | |||||||
| chr9:120644891 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+14483G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644891 | |||||||
| chr9:120644911 | C | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+14463G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644911 | |||||||
| chr9:120644920 | G | C | 1 | a0001c0002t0002g0218 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.803+14454C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120644920 | |||||||
| chr9:120645240 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+14134G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120645240 | |||||||
| chr9:120645241 | G | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803+14133C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120645241 | |||||||
| chr9:120645318 | T | C | 1 | a0001c0002t0021g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.803+14056A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120645318 | |||||||
| chr9:120645327 | T | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+14047A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120645327 | |||||||
| chr9:120645641 | A | C | 1 | a0001c0002t0024g0181 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.803+13733T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120645641 | |||||||
| chr9:120645998 | T | C | 1 | a0002c0006t0001g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.803+13376A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120645998 | |||||||
| chr9:120646016 | C | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+13358G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646016 | |||||||
| chr9:120646081 | T | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+13293A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646081 | |||||||
| chr9:120646126 | A | G | 1 | a0002c0001t0001g0102 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.803+13248T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646126 | |||||||
| chr9:120646140 | G | A | 2 | a0002c0001t0004g0081 a0002c0001t0026g0087 |
2 | NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.803+13234C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646140 | |||||||
| chr9:120646246 | C | T | 15 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(12): Show |
15 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+13128G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646246 | |||||||
| chr9:120646394 | C | A | 4 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+12980G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646394 | |||||||
| chr9:120646410 | T | C | 151 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(148): Show |
151 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.803+12964A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646410 | |||||||
| chr9:120646458 | T | C | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.803+12916A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646458 | |||||||
| chr9:120646709 | T | C | 1 | a0001c0002t0002g0231 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.803+12665A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646709 | |||||||
| chr9:120646804 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+12570G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646804 | |||||||
| chr9:120646900 | T | A | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.803+12474A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120646900 | |||||||
| chr9:120647223 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803+12151A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120647223 | |||||||
| chr9:120647253 | T | G | 18 | a0001c0002t0002g0196 a0001c0002t0002g0270 a0001c0003t0003g0140 others(15): Show |
18 | HG00639.hp1 HG01261.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.803+12121A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120647253 | |||||||
| chr9:120647472 | A | T | 1 | a0002c0001t0001g0018 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.803+11902T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120647472 | |||||||
| chr9:120647586 | T | C | 116 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.803+11788A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120647586 | |||||||
| chr9:120647687 | T | C | 1 | a0002c0001t0001g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.803+11687A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120647687 | |||||||
| chr9:120647776 | T | C | 1 | a0001c0002t0002g0221 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.803+11598A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120647776 | |||||||
| chr9:120647816 | C | G | 1 | a0002c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.803+11558G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120647816 | |||||||
| chr9:120647917 | CTCTCTT | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+11451_803+1145 others(10): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120647917 | |||||||
| chr9:120648007 | C | G | 1 | a0002c0001t0001g0004 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.803+11367G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648007 | |||||||
| chr9:120648122 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+11252G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648122 | |||||||
| chr9:120648135 | C | T | 1 | a0001c0003t0008g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.803+11239G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648135 | |||||||
| chr9:120648147 | C | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+11227G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648147 | |||||||
| chr9:120648162 | A | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.803+11212T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648162 | |||||||
| chr9:120648341 | T | G | 2 | a0002c0001t0007g0091 a0002c0001t0007g0092 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.803+11033A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648341 | |||||||
| chr9:120648434 | G | C | 1 | a0001c0002t0002g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.803+10940C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648434 | |||||||
| chr9:120648541 | C | T | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.803+10833G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648541 | |||||||
| chr9:120648733 | G | A | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+10641C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648733 | |||||||
| chr9:120648891 | T | C | 9 | a0002c0001t0001g0096 a0002c0001t0001g0097 a0002c0001t0001g0098 others(6): Show |
9 | HG01109.hp2 HG01261.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+10483A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648891 | |||||||
| chr9:120648904 | C | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.803+10470G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648904 | |||||||
| chr9:120648958 | G | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+10416C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120648958 | |||||||
| chr9:120649216 | A | C | 1 | a0002c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.803+10158T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120649216 | |||||||
| chr9:120649274 | C | T | 276 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0002t0002g0164 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.803+10100G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120649274 | |||||||
| chr9:120649675 | T | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+9699A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120649675 | |||||||
| chr9:120649776 | C | T | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+9598G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120649776 | |||||||
| chr9:120649817 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+9557C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120649817 | |||||||
| chr9:120649851 | T | C | 1 | a0001c0002t0002g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.803+9523A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120649851 | |||||||
| chr9:120649868 | C | T | 1 | a0002c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.803+9506G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120649868 | |||||||
| chr9:120649885 | A | T | 1 | a0001c0002t0002g0191 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.803+9489T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120649885 | |||||||
| chr9:120650038 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+9336C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650038 | |||||||
| chr9:120650117 | AT | A | 9 | a0002c0001t0001g0109 a0002c0001t0001g0116 a0002c0001t0001g0117 others(6): Show |
9 | HG00558.hp2 HG00621.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+9256delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650117 | |||||||
| chr9:120650126 | G | A | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+9248C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650126 | |||||||
| chr9:120650130 | G | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+9244C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650130 | |||||||
| chr9:120650137 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+9237G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650137 | |||||||
| chr9:120650138 | G | A | 3 | a0002c0001t0001g0025 a0002c0001t0001g0026 a0002c0001t0002g0138 |
3 | HG02155.hp1 NA18964.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.803+9236C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650138 | |||||||
| chr9:120650193 | G | A | 2 | a0001c0002t0002g0190 a0002c0001t0001g0068 |
2 | HG00438.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.803+9181C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650193 | |||||||
| chr9:120650285 | C | T | 151 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(148): Show |
151 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.803+9089G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650285 | |||||||
| chr9:120650470 | C | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+8904G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650470 | |||||||
| chr9:120650491 | GGACATCC others(35): Show |
G | 1 | a0002c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.803+8841_803+8882d others(44): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650491 | |||||||
| chr9:120650524 | T | G | 1 | a0001c0002t0002g0253 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.803+8850A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650524 | |||||||
| chr9:120650526 | C | T | 1 | a0002c0001t0001g0113 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.803+8848G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650526 | |||||||
| chr9:120650592 | T | A | 1 | a0001c0002t0002g0275 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.803+8782A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650592 | |||||||
| chr9:120650784 | T | G | 4 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+8590A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650784 | |||||||
| chr9:120650821 | T | G | 1 | a0002c0001t0001g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803+8553A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120650821 | |||||||
| chr9:120651070 | A | G | 1 | a0002c0001t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.803+8304T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651070 | |||||||
| chr9:120651118 | T | C | 2 | a0001c0003t0003g0159 a0001c0003t0027g0158 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.803+8256A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651118 | |||||||
| chr9:120651145 | T | G | 1 | a0001c0002t0002g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.803+8229A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651145 | |||||||
| chr9:120651179 | T | C | 2 | a0002c0001t0001g0029 a0002c0001t0001g0030 |
2 | NA18967.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.803+8195A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651179 | |||||||
| chr9:120651274 | T | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+8100A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651274 | |||||||
| chr9:120651389 | A | G | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803+7985T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651389 | |||||||
| chr9:120651481 | T | A | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+7893A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651481 | |||||||
| chr9:120651557 | T | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+7817A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651557 | |||||||
| chr9:120651625 | T | C | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.803+7749A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651625 | |||||||
| chr9:120651654 | A | AT | 35 | a0001c0002t0002g0174 a0001c0002t0002g0182 a0001c0002t0002g0268 others(32): Show |
35 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.803+7719dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651654 | |||||||
| chr9:120651746 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+7628G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651746 | |||||||
| chr9:120651802 | G | A | 3 | a0002c0001t0009g0099 a0002c0001t0009g0100 a0002c0001t0009g0101 |
3 | HG01109.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.803+7572C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120651802 | |||||||
| chr9:120652050 | C | A | 1 | a0001c0002t0002g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.803+7324G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652050 | |||||||
| chr9:120652142 | G | A | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.803+7232C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652142 | |||||||
| chr9:120652142 | G | GCA | 5 | a0002c0001t0001g0004 a0002c0001t0001g0019 a0002c0001t0001g0061 others(2): Show |
5 | HG01167.hp2 NA18963.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+7230_803+7231d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652142 | |||||||
| chr9:120652142 | G | GCACA | 4 | a0002c0001t0002g0066 a0002c0001t0002g0067 a0002c0001t0004g0082 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+7228_803+7231d others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652142 | |||||||
| chr9:120652142 | GCA | G | 20 | a0001c0002t0002g0195 a0001c0002t0002g0227 a0001c0002t0002g0234 others(17): Show |
20 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.803+7230_803+7231d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652142 | |||||||
| chr9:120652142 | GCACA | G | 22 | a0001c0003t0003g0140 a0001c0003t0003g0145 a0001c0003t0003g0147 others(19): Show |
23 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.803+7228_803+7231d others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652142 | |||||||
| chr9:120652142 | GCACACA | G | 5 | a0001c0003t0003g0141 a0001c0003t0003g0142 a0001c0003t0027g0158 others(2): Show |
5 | HG00735.hp2 HG01891.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+7226_803+7231d others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652142 | |||||||
| chr9:120652142 | GCACACAC others(3): Show |
G | 1 | a0002c0001t0001g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.803+7222_803+7231d others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652142 | |||||||
| chr9:120652142 | GCACACAC others(7): Show |
G | 2 | a0002c0001t0001g0069 a0002c0001t0001g0105 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.803+7218_803+7231d others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652142 | |||||||
| chr9:120652144 | A | G | 5 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+7230T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652144 | |||||||
| chr9:120652168 | ACAC | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0287 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+7203_803+7205d others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652168 | |||||||
| chr9:120652170 | ACAC | A | 3 | a0001c0003t0003g0143 a0001c0003t0003g0144 a0001c0003t0003g0146 |
3 | HG02647.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.803+7201_803+7203d others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652170 | |||||||
| chr9:120652171 | C | A | 1 | a0001c0002t0012g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803+7203G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652171 | |||||||
| chr9:120652173 | C | A | 6 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+7201G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652173 | |||||||
| chr9:120652175 | C | A | 17 | a0001c0002t0002g0195 a0001c0002t0002g0227 a0001c0002t0002g0234 others(14): Show |
17 | HG01891.hp1 HG02109.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.803+7199G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652175 | |||||||
| chr9:120652175 | C | CAAAA | 6 | a0001c0002t0002g0188 a0001c0002t0002g0190 a0001c0002t0002g0208 others(3): Show |
6 | HG00099.hp2 HG00438.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+7198_803+7199i others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652175 | |||||||
| chr9:120652175 | C | CAAAAA | 8 | a0001c0002t0002g0192 a0001c0002t0002g0197 a0001c0002t0002g0216 others(5): Show |
8 | HG01109.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+7198_803+7199i others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652175 | |||||||
| chr9:120652177 | C | A | 34 | a0001c0002t0002g0188 a0001c0002t0002g0190 a0001c0002t0002g0192 others(31): Show |
34 | HG00099.hp2 HG00438.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.803+7197G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652177 | |||||||
| chr9:120652177 | C | CAAA | 3 | a0001c0002t0001g0189 a0001c0002t0002g0259 a0001c0002t0015g0288 |
3 | HG00609.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.803+7196_803+7197i others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652177 | |||||||
| chr9:120652177 | C | CAAAA | 48 | a0001c0002t0002g0174 a0001c0002t0002g0175 a0001c0002t0002g0176 others(45): Show |
48 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.803+7196_803+7197i others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652177 | |||||||
| chr9:120652177 | C | CAAAAA | 29 | a0001c0002t0002g0164 a0001c0002t0002g0173 a0001c0002t0002g0179 others(26): Show |
29 | HG00597.hp1 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.803+7196_803+7197i others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652177 | |||||||
| chr9:120652178 | AC | A | 3 | a0002c0001t0001g0033 a0002c0001t0001g0073 a0002c0001t0001g0117 |
3 | HG02145.hp1 NA19006.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.803+7195delG | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652178 | |||||||
| chr9:120652179 | C | A | 123 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0173 others(120): Show |
123 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.803+7195G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652179 | |||||||
| chr9:120652179 | C | CAA | 3 | a0002c0001t0001g0013 a0002c0001t0001g0024 a0002c0001t0001g0028 |
3 | HG03017.hp1 HG03195.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.803+7194_803+7195i others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652179 | |||||||
| chr9:120652179 | C | CAAAA | 7 | a0001c0002t0002g0229 a0001c0002t0002g0268 a0001c0002t0006g0204 others(4): Show |
7 | HG02735.hp2 HG02809.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+7194_803+7195i others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652179 | |||||||
| chr9:120652179 | C | CAAAAA | 5 | a0001c0002t0002g0205 a0001c0002t0002g0221 a0001c0002t0002g0264 others(2): Show |
5 | HG01981.hp2 HG03540.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+7194_803+7195i others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652179 | |||||||
| chr9:120652179 | C | CAAAAAA | 8 | a0001c0002t0002g0172 a0001c0002t0002g0180 a0001c0002t0002g0186 others(5): Show |
8 | HG00673.hp2 HG00738.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+7194_803+7195i others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652179 | |||||||
| chr9:120652179 | C | CAAAAAAA | 4 | a0001c0002t0002g0201 a0001c0002t0002g0220 a0001c0002t0002g0242 others(1): Show |
4 | NA18967.hp1 NA18973.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+7194_803+7195i others(9): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652179 | |||||||
| chr9:120652181 | C | A | 180 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0002t0002g0164 others(177): Show |
180 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.803+7193G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652181 | |||||||
| chr9:120652181 | C | CA | 8 | a0002c0001t0001g0009 a0002c0001t0001g0012 a0002c0001t0001g0023 others(5): Show |
8 | HG00408.hp2 HG01099.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+7192dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652181 | |||||||
| chr9:120652181 | C | CACACAAA others(3): Show |
1 | a0001c0010t0005g0169 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.803+7192_803+7193i others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652181 | |||||||
| chr9:120652183 | A | C | 4 | a0002c0001t0001g0039 a0002c0001t0001g0054 a0002c0001t0007g0091 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+7191T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652183 | |||||||
| chr9:120652420 | C | T | 1 | a0002c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.803+6954G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652420 | |||||||
| chr9:120652451 | G | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+6923C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652451 | |||||||
| chr9:120652465 | C | T | 6 | a0002c0001t0001g0110 a0002c0001t0001g0111 a0002c0001t0001g0112 others(3): Show |
6 | NA18954.hp1 NA18980.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+6909G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652465 | |||||||
| chr9:120652478 | T | TA | 52 | a0002c0001t0001g0001 a0002c0001t0001g0012 a0002c0001t0001g0015 others(49): Show |
53 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.803+6895dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652478 | |||||||
| chr9:120652478 | T | TAA | 6 | a0002c0001t0001g0093 a0002c0001t0001g0111 a0002c0001t0001g0117 others(3): Show |
6 | HG01109.hp2 HG02738.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.803+6894_803+6895d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652478 | |||||||
| chr9:120652478 | TAA | T | 25 | a0001c0002t0002g0170 a0001c0002t0002g0197 a0001c0002t0002g0206 others(22): Show |
25 | HG00621.hp2 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.803+6894_803+6895d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652478 | |||||||
| chr9:120652478 | TAAA | T | 113 | a0001c0002t0002g0164 a0001c0002t0002g0172 a0001c0002t0002g0173 others(110): Show |
113 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.803+6893_803+6895d others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652478 | |||||||
| chr9:120652478 | TAAAAA | T | 15 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(12): Show |
15 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+6891_803+6895d others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652478 | |||||||
| chr9:120652549 | G | A | 1 | a0001c0002t0021g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.803+6825C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652549 | |||||||
| chr9:120652555 | G | C | 1 | a0002c0001t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.803+6819C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652555 | |||||||
| chr9:120652590 | G | GCA | 6 | a0001c0002t0002g0182 a0001c0002t0002g0187 a0001c0002t0002g0190 others(3): Show |
6 | HG00438.hp1 HG02132.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+6782_803+6783d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652590 | |||||||
| chr9:120652590 | G | GCACACAC others(1): Show |
7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+6776_803+6783d others(10): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652590 | |||||||
| chr9:120652590 | GCA | G | 10 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(7): Show |
10 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.803+6782_803+6783d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652590 | |||||||
| chr9:120652849 | TTCTA | T | 4 | a0001c0002t0002g0188 a0001c0002t0002g0232 a0001c0002t0002g0233 others(1): Show |
4 | NA18959.hp2 NA18967.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+6521_803+6524d others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120652849 | |||||||
| chr9:120653027 | C | T | 5 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.803+6347G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653027 | |||||||
| chr9:120653042 | A | G | 2 | a0002c0001t0002g0066 a0002c0001t0002g0067 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.803+6332T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653042 | |||||||
| chr9:120653184 | T | C | 4 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+6190A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653184 | |||||||
| chr9:120653322 | T | C | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+6052A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653322 | |||||||
| chr9:120653369 | AT | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+6004delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653369 | |||||||
| chr9:120653374 | A | AT | 4 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+5999dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653374 | |||||||
| chr9:120653377 | T | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+5997A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653377 | |||||||
| chr9:120653377 | TA | T | 6 | a0001c0002t0002g0201 a0001c0003t0003g0159 a0001c0003t0027g0158 others(3): Show |
6 | HG00323.hp2 HG03225.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+5996delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653377 | |||||||
| chr9:120653378 | A | T | 259 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0002t0002g0164 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.803+5996T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653378 | |||||||
| chr9:120653378 | AT | A | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+5995delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653378 | |||||||
| chr9:120653379 | T | A | 7 | a0001c0002t0001g0189 a0001c0004t0005g0165 a0001c0004t0005g0166 others(4): Show |
7 | HG02451.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+5995A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653379 | |||||||
| chr9:120653479 | C | A | 1 | a0002c0001t0025g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.803+5895G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653479 | |||||||
| chr9:120653517 | G | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+5857C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653517 | |||||||
| chr9:120653554 | T | C | 1 | a0002c0001t0001g0044 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.803+5820A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653554 | |||||||
| chr9:120653661 | C | T | 15 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(12): Show |
15 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+5713G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653661 | |||||||
| chr9:120653664 | G | A | 1 | a0001c0003t0003g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.803+5710C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653664 | |||||||
| chr9:120653885 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803+5489G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653885 | |||||||
| chr9:120653911 | T | C | 1 | a0002c0001t0001g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.803+5463A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653911 | |||||||
| chr9:120653924 | A | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+5450T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653924 | |||||||
| chr9:120653966 | G | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+5408C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120653966 | |||||||
| chr9:120654023 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+5351C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654023 | |||||||
| chr9:120654037 | G | A | 4 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+5337C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654037 | |||||||
| chr9:120654380 | G | A | 1 | a0001c0003t0003g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.803+4994C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654380 | |||||||
| chr9:120654487 | T | C | 2 | a0001c0002t0014g0199 a0001c0002t0014g0255 |
2 | NA18975.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.803+4887A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654487 | |||||||
| chr9:120654547 | A | G | 8 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(5): Show |
8 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+4827T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654547 | |||||||
| chr9:120654678 | A | G | 15 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(12): Show |
15 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+4696T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654678 | |||||||
| chr9:120654700 | C | T | 2 | a0002c0001t0001g0096 a0002c0001t0001g0097 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.803+4674G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654700 | |||||||
| chr9:120654773 | G | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+4601C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654773 | |||||||
| chr9:120654928 | T | C | 4 | a0001c0003t0003g0143 a0001c0003t0003g0144 a0001c0003t0003g0145 others(1): Show |
4 | HG02647.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+4446A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120654928 | |||||||
| chr9:120655043 | T | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.803+4331A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655043 | |||||||
| chr9:120655112 | C | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803+4262G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655112 | |||||||
| chr9:120655278 | G | A | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+4096C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655278 | |||||||
| chr9:120655453 | C | A | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803+3921G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655453 | |||||||
| chr9:120655467 | G | A | 1 | a0002c0001t0002g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.803+3907C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655467 | |||||||
| chr9:120655562 | G | T | 1 | a0002c0001t0001g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.803+3812C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655562 | |||||||
| chr9:120655607 | CA | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803+3766delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655607 | |||||||
| chr9:120655618 | T | C | 1 | a0001c0002t0002g0284 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.803+3756A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655618 | |||||||
| chr9:120655912 | C | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.803+3462G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120655912 | |||||||
| chr9:120656117 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+3257T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656117 | |||||||
| chr9:120656299 | G | C | 1 | a0002c0001t0001g0127 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.803+3075C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656299 | |||||||
| chr9:120656308 | G | A | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803+3066C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656308 | |||||||
| chr9:120656452 | C | A | 1 | a0001c0002t0002g0241 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803+2922G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656452 | |||||||
| chr9:120656541 | C | T | 1 | a0002c0001t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.803+2833G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656541 | |||||||
| chr9:120656546 | C | CA | 129 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0172 others(126): Show |
129 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.803+2827dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656546 | |||||||
| chr9:120656546 | C | CAA | 10 | a0001c0002t0002g0170 a0001c0002t0002g0192 a0001c0002t0002g0208 others(7): Show |
10 | HG00609.hp2 HG02132.hp2 HG03942.hp1 others(7): Show |
intron_variant | MODIFIER | c.803+2826_803+2827d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656546 | |||||||
| chr9:120656546 | CA | C | 10 | a0001c0002t0002g0275 a0001c0003t0003g0146 a0001c0004t0005g0165 others(7): Show |
10 | HG01070.hp1 HG01070.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.803+2827delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656546 | |||||||
| chr9:120656546 | CAA | C | 10 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.803+2826_803+2827d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656546 | |||||||
| chr9:120656607 | G | A | 1 | a0002c0001t0001g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.803+2767C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656607 | |||||||
| chr9:120656810 | T | A | 1 | a0001c0002t0002g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803+2564A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656810 | |||||||
| chr9:120656900 | G | A | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.803+2474C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656900 | |||||||
| chr9:120656999 | T | C | 2 | a0002c0001t0001g0069 a0002c0001t0001g0105 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.803+2375A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120656999 | |||||||
| chr9:120657262 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+2112C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120657262 | |||||||
| chr9:120657403 | T | C | 1 | a0002c0001t0009g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.803+1971A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120657403 | |||||||
| chr9:120657679 | A | G | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.803+1695T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120657679 | |||||||
| chr9:120657849 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+1525G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120657849 | |||||||
| chr9:120657919 | A | C | 1 | a0002c0001t0001g0018 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.803+1455T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120657919 | |||||||
| chr9:120657943 | T | A | 2 | a0002c0001t0001g0043 a0002c0001t0001g0126 |
2 | HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.803+1431A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120657943 | |||||||
| chr9:120657990 | C | CT | 17 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(14): Show |
17 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.803+1383dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120657990 | |||||||
| chr9:120658109 | C | T | 19 | a0002c0001t0001g0108 a0002c0001t0001g0109 a0002c0001t0001g0110 others(16): Show |
19 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.803+1265G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120658109 | |||||||
| chr9:120658194 | C | T | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.803+1180G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120658194 | |||||||
| chr9:120658492 | C | G | 3 | a0001c0003t0003g0143 a0001c0003t0003g0144 a0001c0003t0003g0145 |
3 | HG02647.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.803+882G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120658492 | |||||||
| chr9:120658568 | T | C | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.803+806A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120658568 | |||||||
| chr9:120658570 | C | T | 1 | a0001c0003t0003g0140 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803+804G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120658570 | |||||||
| chr9:120658864 | T | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803+510A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120658864 | |||||||
| chr9:120658941 | G | C | 2 | a0002c0001t0001g0069 a0002c0001t0001g0105 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.803+433C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120658941 | |||||||
| chr9:120659278 | C | T | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.803+96G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120659278 | |||||||
| chr9:120659357 | C | T | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.803+17G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 2/5 | chr9 | 120659357 | |||||||
| chr9:120659601 | A | G | 44 | a0002c0001t0001g0041 a0002c0001t0001g0043 a0002c0001t0001g0044 others(41): Show |
44 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.602-26T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120659601 | |||||||
| chr9:120659788 | A | AGT | 52 | a0001c0002t0001g0171 a0001c0003t0003g0140 a0001c0003t0003g0141 others(49): Show |
52 | HG00673.hp1 HG01358.hp2 HG01496.hp1 others(49): Show |
intron_variant | MODIFIER | c.602-215_602-214dup others(2): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120659788 | |||||||
| chr9:120659788 | A | AGTGT | 4 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0003t0027g0158 others(1): Show |
4 | HG02615.hp2 HG03017.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.602-217_602-214dup others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120659788 | |||||||
| chr9:120659788 | A | AGTGTGT | 7 | a0001c0002t0012g0287 a0001c0003t0003g0143 a0001c0003t0003g0144 others(4): Show |
7 | HG00408.hp2 HG02083.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.602-219_602-214dup others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120659788 | |||||||
| chr9:120659788 | AGT | A | 114 | a0001c0002t0002g0164 a0001c0002t0002g0172 a0001c0002t0002g0174 others(111): Show |
114 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.602-215_602-214del others(2): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120659788 | |||||||
| chr9:120659888 | T | C | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-313A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120659888 | |||||||
| chr9:120659973 | G | A | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.602-398C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120659973 | |||||||
| chr9:120660162 | A | G | 1 | a0001c0002t0002g0273 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.602-587T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120660162 | |||||||
| chr9:120660236 | G | A | 4 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(1): Show |
4 | HG00639.hp1 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-661C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120660236 | |||||||
| chr9:120660325 | G | A | 13 | a0002c0001t0001g0108 a0002c0001t0001g0109 a0002c0001t0001g0116 others(10): Show |
13 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.602-750C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120660325 | |||||||
| chr9:120660367 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-792G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120660367 | |||||||
| chr9:120660590 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-1015G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120660590 | |||||||
| chr9:120661091 | A | G | 1 | a0001c0002t0002g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.602-1516T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120661091 | |||||||
| chr9:120661130 | C | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-1555G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120661130 | |||||||
| chr9:120661153 | T | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-1578A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120661153 | |||||||
| chr9:120661402 | C | G | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-1827G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120661402 | |||||||
| chr9:120661402 | C | T | 1 | a0001c0002t0002g0251 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.602-1827G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120661402 | |||||||
| chr9:120661532 | G | A | 1 | a0002c0001t0010g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.602-1957C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120661532 | |||||||
| chr9:120661756 | G | A | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-2181C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120661756 | |||||||
| chr9:120661888 | C | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-2313G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120661888 | |||||||
| chr9:120662094 | A | G | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.602-2519T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120662094 | |||||||
| chr9:120662230 | T | G | 9 | a0001c0002t0002g0192 a0001c0002t0002g0211 a0001c0002t0002g0212 others(6): Show |
9 | HG00323.hp2 HG01070.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-2655A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120662230 | |||||||
| chr9:120662274 | C | T | 153 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(150): Show |
153 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.602-2699G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120662274 | |||||||
| chr9:120662639 | G | T | 2 | a0002c0001t0001g0044 a0002c0001t0001g0052 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.602-3064C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120662639 | |||||||
| chr9:120662837 | G | A | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-3262C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120662837 | |||||||
| chr9:120663056 | T | A | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-3481A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120663056 | |||||||
| chr9:120663659 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-4084A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120663659 | |||||||
| chr9:120663770 | G | A | 1 | a0001c0002t0002g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.602-4195C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120663770 | |||||||
| chr9:120663850 | G | A | 1 | a0002c0001t0004g0083 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.602-4275C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120663850 | |||||||
| chr9:120663978 | G | A | 151 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(148): Show |
151 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.602-4403C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120663978 | |||||||
| chr9:120664086 | G | C | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-4511C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120664086 | |||||||
| chr9:120664623 | G | A | 2 | a0001c0002t0002g0228 a0001c0002t0002g0245 |
2 | HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.602-5048C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120664623 | |||||||
| chr9:120664697 | G | A | 1 | a0001c0002t0002g0251 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.602-5122C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120664697 | |||||||
| chr9:120664968 | A | C | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-5393T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120664968 | |||||||
| chr9:120665071 | A | T | 1 | a0002c0001t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.602-5496T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120665071 | |||||||
| chr9:120665155 | C | T | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-5580G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120665155 | |||||||
| chr9:120665211 | CT | C | 131 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(128): Show |
131 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.602-5637delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120665211 | |||||||
| chr9:120665884 | T | G | 2 | a0002c0001t0001g0043 a0002c0001t0001g0126 |
2 | HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.602-6309A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120665884 | |||||||
| chr9:120665944 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-6369G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120665944 | |||||||
| chr9:120665970 | C | T | 29 | a0002c0001t0001g0044 a0002c0001t0001g0052 a0002c0001t0001g0069 others(26): Show |
29 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-6395G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120665970 | |||||||
| chr9:120666064 | G | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-6489C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666064 | |||||||
| chr9:120666073 | G | T | 21 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(18): Show |
21 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-6498C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666073 | |||||||
| chr9:120666089 | A | C | 2 | a0001c0002t0002g0228 a0001c0002t0002g0245 |
2 | HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.602-6514T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666089 | |||||||
| chr9:120666186 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-6611G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666186 | |||||||
| chr9:120666520 | T | C | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-6945A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666520 | |||||||
| chr9:120666565 | G | A | 1 | a0002c0001t0001g0020 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.602-6990C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666565 | |||||||
| chr9:120666736 | G | A | 1 | a0001c0002t0002g0256 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.602-7161C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666736 | |||||||
| chr9:120666800 | C | T | 151 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(148): Show |
151 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.602-7225G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666800 | |||||||
| chr9:120666850 | T | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-7275A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666850 | |||||||
| chr9:120666858 | A | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-7283T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666858 | |||||||
| chr9:120666933 | G | C | 1 | a0002c0001t0002g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.602-7358C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120666933 | |||||||
| chr9:120667085 | A | G | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-7510T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120667085 | |||||||
| chr9:120667170 | T | C | 1 | a0002c0001t0001g0137 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.602-7595A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120667170 | |||||||
| chr9:120667328 | T | C | 282 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0002t0002g0164 others(279): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.602-7753A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120667328 | |||||||
| chr9:120667665 | T | C | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.602-8090A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120667665 | |||||||
| chr9:120667715 | G | A | 1 | a0002c0001t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.602-8140C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120667715 | |||||||
| chr9:120667808 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-8233G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120667808 | |||||||
| chr9:120667919 | G | A | 2 | a0001c0002t0002g0207 a0001c0002t0002g0208 |
2 | HG02074.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.602-8344C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120667919 | |||||||
| chr9:120668079 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-8504G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120668079 | |||||||
| chr9:120668086 | T | C | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-8511A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120668086 | |||||||
| chr9:120668088 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-8513G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120668088 | |||||||
| chr9:120668306 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-8731A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120668306 | |||||||
| chr9:120668403 | T | C | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-8828A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120668403 | |||||||
| chr9:120668441 | A | C | 3 | a0001c0002t0002g0228 a0001c0002t0002g0245 a0001c0002t0002g0249 |
3 | HG02129.hp1 HG02155.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.602-8866T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120668441 | |||||||
| chr9:120668604 | A | T | 1 | a0002c0001t0007g0091 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-9029T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120668604 | |||||||
| chr9:120668783 | G | A | 1 | a0002c0001t0001g0009 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.602-9208C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120668783 | |||||||
| chr9:120669133 | C | G | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-9558G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669133 | |||||||
| chr9:120669149 | A | C | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.602-9574T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669149 | |||||||
| chr9:120669200 | T | C | 1 | a0002c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.602-9625A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669200 | |||||||
| chr9:120669241 | C | T | 1 | a0002c0001t0001g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.602-9666G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669241 | |||||||
| chr9:120669262 | C | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-9687G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669262 | |||||||
| chr9:120669378 | A | G | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-9803T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669378 | |||||||
| chr9:120669569 | T | A | 1 | a0001c0003t0003g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.602-9994A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669569 | |||||||
| chr9:120669575 | C | CA | 19 | a0001c0002t0002g0237 a0001c0002t0012g0285 a0001c0002t0012g0286 others(16): Show |
19 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-10001dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669575 | |||||||
| chr9:120669624 | A | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-10049T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669624 | |||||||
| chr9:120669707 | T | C | 19 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(16): Show |
19 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-10132A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669707 | |||||||
| chr9:120669771 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-10196G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669771 | |||||||
| chr9:120669914 | G | A | 1 | a0002c0001t0010g0053 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.602-10339C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120669914 | |||||||
| chr9:120670011 | A | C | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.602-10436T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670011 | |||||||
| chr9:120670109 | C | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-10534G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670109 | |||||||
| chr9:120670222 | G | A | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.602-10647C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670222 | |||||||
| chr9:120670372 | C | T | 1 | a0002c0001t0001g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.602-10797G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670372 | |||||||
| chr9:120670426 | T | C | 5 | a0002c0001t0001g0014 a0002c0001t0001g0019 a0002c0001t0001g0027 others(2): Show |
5 | NA18966.hp2 NA18975.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-10851A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670426 | |||||||
| chr9:120670481 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-10906T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670481 | |||||||
| chr9:120670761 | A | G | 116 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.602-11186T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670761 | |||||||
| chr9:120670779 | C | G | 1 | a0001c0002t0014g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.602-11204G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670779 | |||||||
| chr9:120670799 | C | T | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-11224G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670799 | |||||||
| chr9:120670809 | T | C | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-11234A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670809 | |||||||
| chr9:120670900 | C | G | 2 | a0002c0001t0001g0071 a0002c0001t0001g0072 |
2 | HG00438.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.602-11325G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120670900 | |||||||
| chr9:120671476 | C | T | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.602-11901G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120671476 | |||||||
| chr9:120671500 | T | C | 1 | a0002c0001t0004g0086 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.602-11925A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120671500 | |||||||
| chr9:120671541 | T | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-11966A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120671541 | |||||||
| chr9:120671603 | A | T | 2 | a0002c0001t0001g0044 a0002c0001t0001g0052 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.602-12028T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120671603 | |||||||
| chr9:120671658 | G | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-12083C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120671658 | |||||||
| chr9:120671665 | G | A | 4 | a0002c0001t0001g0111 a0002c0001t0001g0113 a0002c0001t0001g0114 others(1): Show |
4 | NA18980.hp2 NA18993.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-12090C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120671665 | |||||||
| chr9:120672038 | A | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-12463T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672038 | |||||||
| chr9:120672220 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-12645T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672220 | |||||||
| chr9:120672301 | A | G | 1 | a0001c0003t0003g0146 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.602-12726T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672301 | |||||||
| chr9:120672316 | G | A | 6 | a0001c0002t0002g0193 a0001c0002t0002g0197 a0001c0002t0002g0198 others(3): Show |
6 | HG01071.hp1 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-12741C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672316 | |||||||
| chr9:120672323 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-12748G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672323 | |||||||
| chr9:120672330 | C | A | 1 | a0002c0001t0001g0015 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.602-12755G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672330 | |||||||
| chr9:120672433 | A | AAAAT | 34 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0003t0003g0140 others(31): Show |
34 | HG00408.hp2 HG00639.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-12862_602-1285 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672433 | |||||||
| chr9:120672433 | A | AAAATAAA others(1): Show |
7 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-12866_602-1285 others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672433 | |||||||
| chr9:120672433 | A | AAAATAAA others(5): Show |
14 | a0001c0002t0015g0288 a0001c0002t0015g0289 a0001c0003t0003g0141 others(11): Show |
14 | HG01243.hp2 HG01891.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.602-12870_602-1285 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672433 | |||||||
| chr9:120672433 | A | AAAATAAA others(9): Show |
2 | a0001c0003t0011g0155 a0001c0004t0005g0168 |
2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.602-12874_602-1285 others(20): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672433 | |||||||
| chr9:120672433 | AAAAT | A | 8 | a0001c0002t0002g0228 a0001c0002t0002g0245 a0001c0002t0002g0249 others(5): Show |
8 | HG01109.hp2 HG02129.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-12862_602-1285 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672433 | |||||||
| chr9:120672433 | AAAATAAA others(1): Show |
A | 114 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(111): Show |
114 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.602-12866_602-1285 others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672433 | |||||||
| chr9:120672433 | AAAATAAA others(5): Show |
A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-12870_602-1285 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672433 | |||||||
| chr9:120672447 | A | C | 1 | a0001c0002t0002g0197 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.602-12872T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672447 | |||||||
| chr9:120672473 | A | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-12898T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672473 | |||||||
| chr9:120672577 | C | T | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.602-13002G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120672577 | |||||||
| chr9:120673091 | T | C | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.602-13516A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673091 | |||||||
| chr9:120673104 | G | A | 1 | a0002c0001t0001g0071 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.602-13529C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673104 | |||||||
| chr9:120673126 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-13551A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673126 | |||||||
| chr9:120673270 | T | C | 1 | a0001c0004t0005g0168 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.602-13695A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673270 | |||||||
| chr9:120673312 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-13737T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673312 | |||||||
| chr9:120673366 | A | G | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.602-13791T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673366 | |||||||
| chr9:120673502 | G | A | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-13927C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673502 | |||||||
| chr9:120673694 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-14119T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673694 | |||||||
| chr9:120673964 | C | T | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.602-14389G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673964 | |||||||
| chr9:120673969 | C | CA | 119 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(116): Show |
119 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.602-14395dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673969 | |||||||
| chr9:120673969 | CA | C | 20 | a0001c0002t0015g0288 a0001c0002t0015g0289 a0001c0003t0003g0140 others(17): Show |
20 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.602-14395delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120673969 | |||||||
| chr9:120674044 | T | C | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.602-14469A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120674044 | |||||||
| chr9:120674160 | T | C | 1 | a0002c0001t0001g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.602-14585A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120674160 | |||||||
| chr9:120674254 | C | T | 2 | a0001c0003t0005g0160 a0001c0003t0005g0161 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-14679G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120674254 | |||||||
| chr9:120674676 | C | T | 1 | a0002c0001t0001g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.602-15101G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120674676 | |||||||
| chr9:120674686 | A | G | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-15111T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120674686 | |||||||
| chr9:120674880 | A | AT | 116 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.602-15306dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120674880 | |||||||
| chr9:120674884 | T | G | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-15309A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120674884 | |||||||
| chr9:120674902 | G | A | 1 | a0002c0001t0001g0022 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.602-15327C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120674902 | |||||||
| chr9:120675024 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-15449T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675024 | |||||||
| chr9:120675206 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-15631G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675206 | |||||||
| chr9:120675439 | A | T | 1 | a0002c0001t0001g0063 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.602-15864T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675439 | |||||||
| chr9:120675550 | G | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-15975C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675550 | |||||||
| chr9:120675586 | C | T | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.602-16011G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675586 | |||||||
| chr9:120675655 | G | GA | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.602-16081dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675655 | |||||||
| chr9:120675671 | A | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-16096T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675671 | |||||||
| chr9:120675690 | C | T | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-16115G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675690 | |||||||
| chr9:120675699 | C | CAAGATGG others(265): Show |
3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-16125_602-1612 others(276): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675699 | |||||||
| chr9:120675749 | G | A | 1 | a0001c0002t0002g0223 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.602-16174C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675749 | |||||||
| chr9:120675756 | C | T | 1 | a0001c0004t0005g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.602-16181G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675756 | |||||||
| chr9:120675761 | G | A | 4 | a0001c0002t0002g0211 a0002c0001t0009g0099 a0002c0001t0009g0100 others(1): Show |
4 | HG01109.hp2 HG02738.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.602-16186C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675761 | |||||||
| chr9:120675837 | G | A | 2 | a0001c0002t0002g0232 a0001c0002t0002g0233 |
2 | NA18959.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.602-16262C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675837 | |||||||
| chr9:120675847 | C | T | 116 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.602-16272G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675847 | |||||||
| chr9:120675867 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-16292C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675867 | |||||||
| chr9:120675874 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-16299G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675874 | |||||||
| chr9:120675887 | C | CA | 114 | a0001c0002t0002g0164 a0001c0002t0002g0173 a0001c0002t0002g0174 others(111): Show |
114 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.602-16313dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675887 | |||||||
| chr9:120675887 | C | CAA | 24 | a0001c0002t0002g0170 a0001c0002t0002g0172 a0001c0002t0002g0179 others(21): Show |
24 | HG00558.hp1 HG00597.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.602-16314_602-1631 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675887 | |||||||
| chr9:120675887 | CA | C | 15 | a0001c0003t0003g0146 a0001c0003t0003g0159 a0001c0003t0008g0152 others(12): Show |
15 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.602-16313delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675887 | |||||||
| chr9:120675887 | CAA | C | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.602-16314_602-1631 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675887 | |||||||
| chr9:120675902 | A | C | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.602-16327T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675902 | |||||||
| chr9:120675908 | A | C | 1 | a0002c0001t0001g0009 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.602-16333T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675908 | |||||||
| chr9:120675911 | C | A | 1 | a0001c0002t0002g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.602-16336G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120675911 | |||||||
| chr9:120676191 | G | A | 1 | a0002c0001t0001g0040 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.602-16616C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676191 | |||||||
| chr9:120676214 | T | C | 1 | a0001c0002t0002g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.602-16639A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676214 | |||||||
| chr9:120676251 | C | T | 2 | a0002c0001t0002g0066 a0002c0001t0002g0067 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.602-16676G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676251 | |||||||
| chr9:120676444 | CA | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-16870delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676444 | |||||||
| chr9:120676461 | T | C | 2 | a0002c0001t0002g0066 a0002c0001t0002g0067 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.602-16886A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676461 | |||||||
| chr9:120676811 | G | T | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.602-17236C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676811 | |||||||
| chr9:120676888 | A | G | 7 | a0001c0002t0002g0277 a0001c0002t0002g0278 a0001c0002t0002g0279 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.602-17313T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676888 | |||||||
| chr9:120676918 | G | A | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.602-17343C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676918 | |||||||
| chr9:120676955 | G | C | 1 | a0001c0002t0002g0243 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.602-17380C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120676955 | |||||||
| chr9:120677025 | T | C | 1 | a0002c0001t0002g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.602-17450A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677025 | |||||||
| chr9:120677049 | T | A | 1 | a0002c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.602-17474A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677049 | |||||||
| chr9:120677066 | A | G | 1 | a0002c0001t0001g0065 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.602-17491T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677066 | |||||||
| chr9:120677126 | AGT | A | 276 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0002t0002g0164 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.602-17553_602-1755 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677126 | |||||||
| chr9:120677191 | C | T | 1 | a0002c0001t0001g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.602-17616G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677191 | |||||||
| chr9:120677221 | T | C | 18 | a0001c0002t0015g0288 a0001c0002t0015g0289 a0001c0003t0003g0140 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.602-17646A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677221 | |||||||
| chr9:120677273 | C | T | 1 | a0001c0002t0002g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.602-17698G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677273 | |||||||
| chr9:120677307 | A | T | 1 | a0002c0001t0001g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.602-17732T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677307 | |||||||
| chr9:120677308 | T | A | 4 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(1): Show |
4 | HG02615.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-17733A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677308 | |||||||
| chr9:120677611 | T | C | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.602-18036A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677611 | |||||||
| chr9:120677682 | C | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-18107G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677682 | |||||||
| chr9:120677801 | G | T | 3 | a0001c0002t0002g0195 a0001c0002t0002g0227 a0001c0002t0002g0234 |
3 | HG02165.hp2 NA19060.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.602-18226C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677801 | |||||||
| chr9:120677907 | C | T | 1 | a0002c0001t0007g0090 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.602-18332G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677907 | |||||||
| chr9:120677940 | C | T | 5 | a0002c0001t0001g0002 a0002c0001t0001g0005 a0002c0001t0001g0006 others(2): Show |
5 | HG02040.hp1 HG02523.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-18365G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120677940 | |||||||
| chr9:120678461 | C | CTT | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-18888_602-1888 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120678461 | |||||||
| chr9:120678597 | T | G | 86 | a0001c0002t0002g0170 a0001c0002t0002g0172 a0001c0002t0002g0173 others(83): Show |
86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.602-19022A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120678597 | |||||||
| chr9:120678611 | A | T | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.602-19036T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120678611 | |||||||
| chr9:120678766 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-19191T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120678766 | |||||||
| chr9:120678945 | C | G | 3 | a0001c0002t0002g0175 a0001c0002t0002g0176 a0001c0002t0024g0181 |
3 | HG01081.hp1 HG01168.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.602-19370G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120678945 | |||||||
| chr9:120679061 | G | A | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-19486C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679061 | |||||||
| chr9:120679097 | T | C | 184 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(181): Show |
184 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.602-19522A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679097 | |||||||
| chr9:120679109 | G | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.602-19534C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679109 | |||||||
| chr9:120679348 | A | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.602-19773T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679348 | |||||||
| chr9:120679463 | G | A | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-19888C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679463 | |||||||
| chr9:120679480 | G | C | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.602-19905C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679480 | |||||||
| chr9:120679496 | G | A | 3 | a0002c0001t0010g0053 a0002c0001t0010g0094 a0002c0001t0010g0095 |
3 | HG01099.hp2 HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.602-19921C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679496 | |||||||
| chr9:120679589 | G | A | 1 | a0001c0010t0005g0169 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.602-20014C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679589 | |||||||
| chr9:120679626 | A | T | 2 | a0001c0002t0014g0199 a0001c0002t0014g0255 |
2 | NA18975.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.602-20051T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679626 | |||||||
| chr9:120679738 | G | A | 1 | a0001c0002t0002g0222 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.602-20163C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679738 | |||||||
| chr9:120679749 | C | T | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-20174G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679749 | |||||||
| chr9:120679756 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-20181T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679756 | |||||||
| chr9:120679937 | C | CA | 116 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.602-20363dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679937 | |||||||
| chr9:120679937 | CA | C | 17 | a0001c0002t0001g0189 a0001c0003t0003g0140 a0001c0003t0003g0141 others(14): Show |
17 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.602-20363delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679937 | |||||||
| chr9:120679953 | A | G | 19 | a0002c0001t0001g0108 a0002c0001t0001g0109 a0002c0001t0001g0110 others(16): Show |
19 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-20378T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120679953 | |||||||
| chr9:120680040 | T | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-20465A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680040 | |||||||
| chr9:120680317 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-20742C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680317 | |||||||
| chr9:120680388 | A | AC | 4 | a0001c0002t0002g0222 a0001c0002t0002g0249 a0002c0001t0001g0114 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-20814dupG | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680388 | |||||||
| chr9:120680456 | C | A | 15 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(12): Show |
15 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.602-20881G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680456 | |||||||
| chr9:120680662 | T | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-21087A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680662 | |||||||
| chr9:120680671 | A | T | 1 | a0002c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.602-21096T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680671 | |||||||
| chr9:120680706 | C | T | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.602-21131G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680706 | |||||||
| chr9:120680768 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-21193G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680768 | |||||||
| chr9:120680813 | C | T | 1 | a0001c0003t0005g0160 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.602-21238G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680813 | |||||||
| chr9:120680865 | G | A | 1 | a0002c0001t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.602-21290C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120680865 | |||||||
| chr9:120681050 | A | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-21475T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681050 | |||||||
| chr9:120681076 | C | T | 1 | a0002c0001t0001g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.602-21501G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681076 | |||||||
| chr9:120681174 | G | A | 1 | a0001c0002t0002g0174 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.602-21599C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681174 | |||||||
| chr9:120681344 | T | C | 12 | a0002c0001t0001g0078 a0002c0001t0001g0084 a0002c0001t0004g0079 others(9): Show |
12 | HG00609.hp1 HG02132.hp1 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.602-21769A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681344 | |||||||
| chr9:120681369 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-21794T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681369 | |||||||
| chr9:120681498 | G | C | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.602-21923C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681498 | |||||||
| chr9:120681572 | G | GA | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.602-21998dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681572 | |||||||
| chr9:120681708 | G | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-22133C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681708 | |||||||
| chr9:120681737 | C | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-22162G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681737 | |||||||
| chr9:120681818 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-22243G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681818 | |||||||
| chr9:120681915 | G | A | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-22340C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120681915 | |||||||
| chr9:120682309 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-22734C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682309 | |||||||
| chr9:120682426 | G | A | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-22851C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682426 | |||||||
| chr9:120682447 | A | T | 1 | a0001c0002t0002g0174 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.602-22872T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682447 | |||||||
| chr9:120682572 | T | TAC | 136 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(133): Show |
136 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.602-22999_602-2299 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682572 | |||||||
| chr9:120682590 | C | CAG | 3 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0257 |
3 | NA18973.hp2 NA19064.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.602-23016_602-2301 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682590 | |||||||
| chr9:120682615 | G | T | 1 | a0001c0002t0024g0181 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.602-23040C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682615 | |||||||
| chr9:120682705 | C | T | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-23130G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682705 | |||||||
| chr9:120682756 | T | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.602-23181A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682756 | |||||||
| chr9:120682794 | G | A | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.602-23219C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120682794 | |||||||
| chr9:120683292 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-23717G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120683292 | |||||||
| chr9:120683334 | G | GCT | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-23761_602-2376 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120683334 | |||||||
| chr9:120683563 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-23988C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120683563 | |||||||
| chr9:120683660 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-24085C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120683660 | |||||||
| chr9:120683777 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-24202G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120683777 | |||||||
| chr9:120683858 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-24283G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120683858 | |||||||
| chr9:120684047 | C | T | 115 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(112): Show |
115 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.602-24472G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684047 | |||||||
| chr9:120684309 | C | T | 1 | a0001c0002t0002g0221 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.602-24734G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684309 | |||||||
| chr9:120684429 | CT | C | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-24855delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684429 | |||||||
| chr9:120684530 | C | T | 19 | a0002c0001t0001g0108 a0002c0001t0001g0109 a0002c0001t0001g0110 others(16): Show |
19 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.602-24955G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684530 | |||||||
| chr9:120684679 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-25104G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684679 | |||||||
| chr9:120684680 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-25105G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684680 | |||||||
| chr9:120684839 | C | CT | 8 | a0001c0002t0001g0189 a0001c0003t0008g0150 a0001c0003t0008g0151 others(5): Show |
8 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.602-25265dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684839 | |||||||
| chr9:120684863 | T | A | 6 | a0002c0001t0001g0096 a0002c0001t0001g0097 a0002c0001t0001g0098 others(3): Show |
6 | HG01261.hp1 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-25288A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684863 | |||||||
| chr9:120684946 | T | C | 114 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(111): Show |
114 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.602-25371A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684946 | |||||||
| chr9:120684975 | C | A | 1 | a0001c0002t0002g0185 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.602-25400G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684975 | |||||||
| chr9:120684979 | C | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-25404G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684979 | |||||||
| chr9:120684991 | C | T | 1 | a0001c0003t0005g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.602-25416G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120684991 | |||||||
| chr9:120685081 | G | T | 1 | a0002c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.602-25506C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685081 | |||||||
| chr9:120685122 | C | T | 1 | a0001c0010t0005g0169 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.602-25547G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685122 | |||||||
| chr9:120685130 | G | A | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.602-25555C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685130 | |||||||
| chr9:120685198 | T | C | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-25623A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685198 | |||||||
| chr9:120685230 | T | C | 1 | a0001c0010t0005g0169 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.602-25655A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685230 | |||||||
| chr9:120685436 | C | G | 2 | a0002c0001t0002g0066 a0002c0001t0002g0067 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.602-25861G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685436 | |||||||
| chr9:120685631 | T | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-26056A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685631 | |||||||
| chr9:120685766 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.602-26191G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685766 | |||||||
| chr9:120685771 | T | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-26196A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685771 | |||||||
| chr9:120685963 | G | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.602-26388C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120685963 | |||||||
| chr9:120686034 | T | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-26459A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686034 | |||||||
| chr9:120686087 | A | AT | 23 | a0001c0002t0002g0192 a0001c0002t0002g0269 a0001c0002t0002g0283 others(20): Show |
23 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.602-26513dupA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686087 | |||||||
| chr9:120686087 | AT | A | 11 | a0001c0002t0001g0189 a0001c0002t0015g0288 a0001c0002t0015g0289 others(8): Show |
11 | HG01169.hp1 HG01243.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.602-26513delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686087 | |||||||
| chr9:120686151 | G | A | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.602-26576C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686151 | |||||||
| chr9:120686225 | G | C | 1 | a0002c0001t0001g0051 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.602-26650C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686225 | |||||||
| chr9:120686480 | A | G | 1 | a0001c0010t0005g0169 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.602-26905T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686480 | |||||||
| chr9:120686517 | T | G | 1 | a0001c0002t0002g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.602-26942A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686517 | |||||||
| chr9:120686716 | T | C | 2 | a0002c0001t0001g0096 a0002c0001t0001g0097 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.601+27042A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686716 | |||||||
| chr9:120686792 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+26966T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686792 | |||||||
| chr9:120686947 | T | TTG | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+26809_601+2681 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686947 | |||||||
| chr9:120686947 | T | TTGTGTGT others(1): Show |
3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+26803_601+2681 others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686947 | |||||||
| chr9:120686969 | G | GTA | 11 | a0002c0001t0001g0001 a0002c0001t0001g0015 a0002c0001t0001g0042 others(8): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+26787_601+2678 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120686969 | |||||||
| chr9:120687290 | T | C | 1 | a0001c0002t0002g0186 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.601+26468A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687290 | |||||||
| chr9:120687504 | T | C | 1 | a0002c0001t0001g0031 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.601+26254A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687504 | |||||||
| chr9:120687568 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+26190G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687568 | |||||||
| chr9:120687636 | T | G | 2 | a0001c0003t0005g0160 a0001c0003t0005g0161 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+26122A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687636 | |||||||
| chr9:120687670 | C | CTG | 30 | a0001c0002t0001g0189 a0001c0002t0015g0288 a0001c0002t0015g0289 others(27): Show |
30 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.601+26086_601+2608 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | C | CTGTG | 17 | a0002c0001t0001g0054 a0002c0001t0001g0068 a0002c0001t0001g0096 others(14): Show |
17 | HG00597.hp2 HG01099.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.601+26084_601+2608 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | C | CTGTGTG | 22 | a0001c0010t0005g0169 a0002c0001t0001g0013 a0002c0001t0001g0017 others(19): Show |
22 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.601+26082_601+2608 others(10): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | C | CTGTGTGT others(1): Show |
24 | a0001c0002t0001g0171 a0002c0001t0001g0014 a0002c0001t0001g0019 others(21): Show |
24 | HG00323.hp1 HG00673.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.601+26080_601+2608 others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | C | CTGTGTGT others(3): Show |
32 | a0002c0001t0001g0002 a0002c0001t0001g0004 a0002c0001t0001g0006 others(29): Show |
32 | HG00438.hp2 HG00609.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.601+26078_601+2608 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | C | CTGTGTGT others(5): Show |
6 | a0002c0001t0001g0003 a0002c0001t0001g0005 a0002c0001t0001g0102 others(3): Show |
6 | NA18962.hp1 NA18964.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+26076_601+2608 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | CTG | C | 4 | a0001c0003t0003g0159 a0001c0003t0008g0151 a0001c0003t0008g0152 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+26086_601+2608 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | CTGTG | C | 13 | a0001c0002t0002g0194 a0001c0002t0002g0245 a0001c0002t0002g0249 others(10): Show |
13 | HG00558.hp1 HG00642.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.601+26084_601+2608 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | CTGTGTG | C | 122 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(119): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.601+26082_601+2608 others(10): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | CTGTGTGT others(1): Show |
C | 13 | a0001c0002t0002g0182 a0001c0002t0002g0195 a0001c0002t0002g0234 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.601+26080_601+2608 others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687670 | CTGTGTGT others(3): Show |
C | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.601+26078_601+2608 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687670 | |||||||
| chr9:120687759 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+25999C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687759 | |||||||
| chr9:120687782 | TA | T | 25 | a0001c0002t0001g0189 a0001c0002t0015g0288 a0001c0002t0015g0289 others(22): Show |
25 | HG00408.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.601+25975delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687782 | |||||||
| chr9:120687782 | TAA | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+25974_601+2597 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687782 | |||||||
| chr9:120687783 | A | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+25975T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687783 | |||||||
| chr9:120687877 | C | G | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.601+25881G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120687877 | |||||||
| chr9:120688130 | A | AAC | 22 | a0001c0002t0002g0164 a0001c0002t0002g0193 a0001c0002t0002g0198 others(19): Show |
22 | HG00609.hp1 HG01071.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.601+25626_601+2562 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688130 | |||||||
| chr9:120688130 | A | AACAC | 5 | a0001c0002t0002g0190 a0001c0002t0002g0197 a0001c0002t0002g0203 others(2): Show |
5 | HG00408.hp1 HG00438.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+25624_601+2562 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688130 | |||||||
| chr9:120688130 | AAC | A | 92 | a0001c0002t0002g0170 a0001c0002t0002g0172 a0001c0002t0002g0173 others(89): Show |
92 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.601+25626_601+2562 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688130 | |||||||
| chr9:120688130 | AACAC | A | 33 | a0001c0002t0002g0235 a0001c0002t0002g0236 a0001c0002t0002g0242 others(30): Show |
33 | HG00438.hp2 HG01109.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.601+25624_601+2562 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688130 | |||||||
| chr9:120688130 | AACACAC | A | 14 | a0001c0002t0002g0256 a0001c0002t0012g0287 a0001c0002t0015g0288 others(11): Show |
14 | HG00642.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.601+25622_601+2562 others(10): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688130 | |||||||
| chr9:120688130 | AACACACA others(1): Show |
A | 4 | a0001c0003t0003g0147 a0001c0003t0018g0157 a0002c0001t0001g0072 others(1): Show |
4 | HG00621.hp1 HG00639.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+25620_601+2562 others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688130 | |||||||
| chr9:120688130 | AACACACA others(3): Show |
A | 17 | a0002c0001t0001g0108 a0002c0001t0001g0109 a0002c0001t0001g0110 others(14): Show |
17 | HG00558.hp2 HG00597.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.601+25618_601+2562 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688130 | |||||||
| chr9:120688130 | AACACACA others(5): Show |
A | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.601+25616_601+2562 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688130 | |||||||
| chr9:120688159 | ACACACAC others(5): Show |
A | 7 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+25587_601+2559 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688159 | |||||||
| chr9:120688161 | ACACACAC others(3): Show |
A | 1 | a0001c0003t0019g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601+25587_601+2559 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688161 | |||||||
| chr9:120688167 | A | ACACG | 4 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0039 others(1): Show |
4 | HG02280.hp2 HG02965.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+25587_601+2559 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688167 | |||||||
| chr9:120688167 | A | G | 3 | a0001c0002t0002g0220 a0002c0001t0001g0024 a0002c0001t0001g0065 |
3 | HG03017.hp1 HG03017.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.601+25591T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688167 | |||||||
| chr9:120688212 | T | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+25546A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688212 | |||||||
| chr9:120688573 | C | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+25185G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688573 | |||||||
| chr9:120688593 | T | A | 8 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+25165A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688593 | |||||||
| chr9:120688683 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+25075A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688683 | |||||||
| chr9:120688688 | A | G | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+25070T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688688 | |||||||
| chr9:120688753 | CAGG | C | 4 | a0001c0002t0002g0279 a0001c0002t0002g0281 a0001c0002t0002g0283 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+25002_601+2500 others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688753 | |||||||
| chr9:120688825 | C | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+24933G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688825 | |||||||
| chr9:120688842 | T | C | 1 | a0002c0001t0001g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+24916A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688842 | |||||||
| chr9:120688859 | G | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+24899C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688859 | |||||||
| chr9:120688871 | A | C | 1 | a0002c0001t0001g0037 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.601+24887T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688871 | |||||||
| chr9:120688938 | A | G | 3 | a0002c0001t0001g0134 a0002c0001t0001g0135 a0002c0001t0001g0136 |
3 | HG02109.hp2 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.601+24820T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120688938 | |||||||
| chr9:120689024 | A | G | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+24734T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689024 | |||||||
| chr9:120689075 | TA | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+24682delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689075 | |||||||
| chr9:120689127 | A | G | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.601+24631T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689127 | |||||||
| chr9:120689300 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+24458T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689300 | |||||||
| chr9:120689322 | T | C | 1 | a0001c0002t0002g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.601+24436A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689322 | |||||||
| chr9:120689354 | G | A | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+24404C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689354 | |||||||
| chr9:120689369 | T | C | 1 | a0002c0001t0001g0034 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.601+24389A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689369 | |||||||
| chr9:120689416 | C | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+24342G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689416 | |||||||
| chr9:120689457 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+24301G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689457 | |||||||
| chr9:120689457 | CT | C | 13 | a0002c0001t0001g0084 a0002c0001t0004g0079 a0002c0001t0004g0080 others(10): Show |
13 | HG00609.hp1 HG02055.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.601+24300delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689457 | |||||||
| chr9:120689538 | C | G | 1 | a0001c0003t0008g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.601+24220G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689538 | |||||||
| chr9:120689556 | T | A | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+24202A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689556 | |||||||
| chr9:120689866 | C | T | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+23892G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689866 | |||||||
| chr9:120689922 | C | CTACCCGT | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+23829_601+2383 others(11): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689922 | |||||||
| chr9:120689945 | G | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+23813C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120689945 | |||||||
| chr9:120690007 | A | G | 6 | a0002c0001t0001g0110 a0002c0001t0001g0111 a0002c0001t0001g0112 others(3): Show |
6 | NA18954.hp1 NA18980.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+23751T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120690007 | |||||||
| chr9:120690204 | G | A | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+23554C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120690204 | |||||||
| chr9:120690557 | T | C | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+23201A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120690557 | |||||||
| chr9:120690694 | T | C | 4 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+23064A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120690694 | |||||||
| chr9:120690888 | AAAT | A | 8 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+22867_601+2286 others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120690888 | |||||||
| chr9:120691003 | T | C | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.601+22755A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691003 | |||||||
| chr9:120691034 | G | A | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.601+22724C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691034 | |||||||
| chr9:120691078 | C | T | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.601+22680G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691078 | |||||||
| chr9:120691106 | T | C | 21 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(18): Show |
21 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.601+22652A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691106 | |||||||
| chr9:120691160 | G | T | 1 | a0002c0001t0001g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+22598C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691160 | |||||||
| chr9:120691339 | T | C | 1 | a0002c0001t0001g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.601+22419A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691339 | |||||||
| chr9:120691473 | C | T | 1 | a0001c0008t0002g0163 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.601+22285G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691473 | |||||||
| chr9:120691560 | C | T | 1 | a0002c0001t0001g0035 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.601+22198G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691560 | |||||||
| chr9:120691562 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+22196G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691562 | |||||||
| chr9:120691807 | G | T | 1 | a0002c0001t0001g0074 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.601+21951C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691807 | |||||||
| chr9:120691819 | C | T | 1 | a0001c0002t0002g0215 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.601+21939G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691819 | |||||||
| chr9:120691878 | A | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+21880T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691878 | |||||||
| chr9:120691968 | T | G | 3 | a0001c0002t0002g0164 a0001c0002t0002g0241 a0001c0002t0002g0269 |
3 | HG01891.hp2 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.601+21790A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120691968 | |||||||
| chr9:120692096 | G | C | 11 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(8): Show |
11 | HG02572.hp2 HG02809.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.601+21662C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692096 | |||||||
| chr9:120692299 | A | G | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+21459T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692299 | |||||||
| chr9:120692435 | A | G | 1 | a0001c0002t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.601+21323T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692435 | |||||||
| chr9:120692714 | T | C | 2 | a0002c0001t0001g0069 a0002c0001t0001g0105 |
2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.601+21044A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692714 | |||||||
| chr9:120692724 | G | C | 1 | a0002c0001t0001g0017 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.601+21034C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692724 | |||||||
| chr9:120692792 | C | G | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+20966G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692792 | |||||||
| chr9:120692820 | A | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+20938T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692820 | |||||||
| chr9:120692922 | T | C | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+20836A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692922 | |||||||
| chr9:120692983 | T | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+20775A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120692983 | |||||||
| chr9:120693005 | A | T | 1 | a0001c0002t0002g0275 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.601+20753T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693005 | |||||||
| chr9:120693128 | T | C | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.601+20630A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693128 | |||||||
| chr9:120693275 | C | CA | 19 | a0001c0002t0002g0174 a0001c0002t0002g0182 a0001c0002t0002g0212 others(16): Show |
19 | HG00323.hp2 HG01261.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.601+20482dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693275 | |||||||
| chr9:120693275 | C | CAA | 99 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(96): Show |
99 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.601+20481_601+2048 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693275 | |||||||
| chr9:120693275 | C | CAAA | 8 | a0001c0002t0002g0187 a0001c0002t0002g0196 a0001c0002t0002g0211 others(5): Show |
8 | HG01981.hp1 HG02129.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+20480_601+2048 others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693275 | |||||||
| chr9:120693293 | AAG | A | 8 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+20463_601+2046 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693293 | |||||||
| chr9:120693295 | G | A | 1 | a0001c0003t0005g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.601+20463C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693295 | |||||||
| chr9:120693504 | G | A | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+20254C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693504 | |||||||
| chr9:120693555 | T | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+20203A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693555 | |||||||
| chr9:120693606 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+20152C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693606 | |||||||
| chr9:120693717 | C | T | 1 | a0002c0001t0001g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.601+20041G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693717 | |||||||
| chr9:120693725 | C | T | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.601+20033G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693725 | |||||||
| chr9:120693826 | T | C | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+19932A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693826 | |||||||
| chr9:120693924 | TA | T | 9 | a0001c0002t0002g0172 a0001c0002t0002g0200 a0001c0002t0002g0201 others(6): Show |
9 | HG02040.hp2 HG02965.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.601+19833delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693924 | |||||||
| chr9:120693924 | TAA | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+19832_601+1983 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693924 | |||||||
| chr9:120693980 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+19778T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120693980 | |||||||
| chr9:120694058 | T | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+19700A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120694058 | |||||||
| chr9:120694109 | G | A | 3 | a0002c0001t0009g0099 a0002c0001t0009g0100 a0002c0001t0009g0101 |
3 | HG01109.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.601+19649C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120694109 | |||||||
| chr9:120694125 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+19633T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120694125 | |||||||
| chr9:120694457 | A | G | 2 | a0002c0001t0013g0076 a0002c0001t0013g0077 |
2 | NA18977.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.601+19301T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120694457 | |||||||
| chr9:120694491 | T | C | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+19267A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120694491 | |||||||
| chr9:120694554 | G | C | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+19204C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120694554 | |||||||
| chr9:120694576 | T | C | 1 | a0001c0002t0002g0237 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.601+19182A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120694576 | |||||||
| chr9:120694937 | G | GATAA | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.601+18817_601+1882 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120694937 | |||||||
| chr9:120695036 | TA | T | 6 | a0001c0002t0002g0175 a0001c0002t0006g0265 a0001c0002t0014g0199 others(3): Show |
6 | HG01081.hp1 HG02451.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+18721delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695036 | |||||||
| chr9:120695189 | T | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+18569A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695189 | |||||||
| chr9:120695263 | A | G | 1 | a0001c0002t0002g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.601+18495T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695263 | |||||||
| chr9:120695326 | T | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+18432A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695326 | |||||||
| chr9:120695332 | G | A | 1 | a0001c0002t0021g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.601+18426C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695332 | |||||||
| chr9:120695360 | C | T | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+18398G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695360 | |||||||
| chr9:120695455 | A | T | 4 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+18303T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695455 | |||||||
| chr9:120695489 | A | G | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.601+18269T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695489 | |||||||
| chr9:120695596 | C | T | 138 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(135): Show |
138 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.601+18162G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695596 | |||||||
| chr9:120695603 | C | CA | 41 | a0001c0002t0002g0172 a0001c0002t0002g0180 a0001c0002t0002g0239 others(38): Show |
41 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.601+18154dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | C | CAAAAAAA others(3): Show |
1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.601+18145_601+1815 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | C | CAAAAAAA others(4): Show |
2 | a0001c0003t0003g0143 a0001c0003t0019g0148 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.601+18144_601+1815 others(15): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | C | CAAAAAAA others(5): Show |
2 | a0001c0003t0003g0140 a0001c0003t0018g0157 |
2 | HG00639.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.601+18143_601+1815 others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | C | CAAAAAAA others(6): Show |
2 | a0001c0003t0003g0144 a0001c0003t0003g0145 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.601+18142_601+1815 others(17): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | C | CAAAAAAA others(7): Show |
1 | a0001c0003t0003g0146 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.601+18141_601+1815 others(18): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | CA | C | 19 | a0001c0002t0001g0189 a0001c0002t0002g0212 a0001c0002t0002g0213 others(16): Show |
19 | HG00642.hp2 HG00738.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.601+18154delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | CAA | C | 11 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(8): Show |
11 | HG02809.hp1 HG02965.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.601+18153_601+1815 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | CAAAAAAA others(3): Show |
C | 2 | a0001c0003t0003g0159 a0001c0003t0027g0158 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.601+18145_601+1815 others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695603 | CAAAAAAA others(4): Show |
C | 2 | a0001c0003t0003g0141 a0001c0003t0003g0142 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.601+18144_601+1815 others(15): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695603 | |||||||
| chr9:120695665 | T | C | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+18093A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695665 | |||||||
| chr9:120695700 | A | G | 1 | a0002c0001t0001g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.601+18058T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695700 | |||||||
| chr9:120695730 | T | TGG | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+18026_601+1802 others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695730 | |||||||
| chr9:120695740 | C | T | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+18018G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695740 | |||||||
| chr9:120695903 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+17855T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120695903 | |||||||
| chr9:120696213 | A | G | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+17545T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120696213 | |||||||
| chr9:120696290 | G | A | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+17468C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120696290 | |||||||
| chr9:120696396 | T | C | 5 | a0001c0002t0006g0210 a0001c0002t0006g0258 a0001c0002t0006g0265 others(2): Show |
5 | NA18971.hp1 NA18984.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+17362A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120696396 | |||||||
| chr9:120696402 | T | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+17356A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120696402 | |||||||
| chr9:120696412 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+17346G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120696412 | |||||||
| chr9:120696550 | G | A | 1 | a0002c0001t0010g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+17208C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120696550 | |||||||
| chr9:120696569 | GCTTT | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+17185_601+1718 others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120696569 | |||||||
| chr9:120696694 | G | C | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+17064C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120696694 | |||||||
| chr9:120697239 | T | C | 1 | a0002c0001t0001g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+16519A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120697239 | |||||||
| chr9:120697420 | ATTT | A | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.601+16335_601+1633 others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120697420 | |||||||
| chr9:120697568 | T | A | 12 | a0002c0001t0001g0078 a0002c0001t0001g0084 a0002c0001t0004g0079 others(9): Show |
12 | HG00609.hp1 HG02132.hp1 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+16190A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120697568 | |||||||
| chr9:120697578 | A | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+16180T>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120697578 | |||||||
| chr9:120697596 | C | T | 8 | a0002c0001t0001g0015 a0002c0001t0001g0042 a0002c0001t0001g0046 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+16162G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120697596 | |||||||
| chr9:120697629 | G | C | 1 | a0001c0003t0008g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.601+16129C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120697629 | |||||||
| chr9:120697990 | C | T | 1 | a0002c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.601+15768G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120697990 | |||||||
| chr9:120698222 | G | A | 1 | a0001c0002t0002g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.601+15536C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120698222 | |||||||
| chr9:120698396 | C | T | 15 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(12): Show |
15 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+15362G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120698396 | |||||||
| chr9:120698491 | A | C | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.601+15267T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120698491 | |||||||
| chr9:120698538 | G | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+15220C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120698538 | |||||||
| chr9:120698775 | A | G | 1 | a0002c0001t0001g0109 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.601+14983T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120698775 | |||||||
| chr9:120699096 | A | G | 2 | a0002c0001t0002g0066 a0002c0001t0002g0067 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.601+14662T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120699096 | |||||||
| chr9:120699345 | T | A | 1 | a0001c0002t0002g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.601+14413A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120699345 | |||||||
| chr9:120699351 | G | A | 4 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+14407C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120699351 | |||||||
| chr9:120699556 | A | G | 17 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(14): Show |
17 | HG00597.hp2 HG00639.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.601+14202T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120699556 | |||||||
| chr9:120699724 | T | TA | 13 | a0001c0002t0002g0170 a0001c0002t0002g0183 a0001c0002t0002g0185 others(10): Show |
13 | HG00099.hp2 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.601+14033dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120699724 | |||||||
| chr9:120699823 | T | C | 4 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+13935A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120699823 | |||||||
| chr9:120699891 | C | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+13867G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120699891 | |||||||
| chr9:120700295 | G | A | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+13463C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120700295 | |||||||
| chr9:120700608 | A | G | 1 | a0001c0002t0014g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.601+13150T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120700608 | |||||||
| chr9:120700640 | C | T | 1 | a0001c0002t0002g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.601+13118G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120700640 | |||||||
| chr9:120700755 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.601+13003G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120700755 | |||||||
| chr9:120700897 | G | A | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.601+12861C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120700897 | |||||||
| chr9:120701115 | T | C | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.601+12643A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701115 | |||||||
| chr9:120701140 | C | A | 2 | a0001c0003t0003g0141 a0001c0003t0003g0142 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.601+12618G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701140 | |||||||
| chr9:120701198 | C | T | 11 | a0002c0001t0001g0001 a0002c0001t0001g0015 a0002c0001t0001g0042 others(8): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+12560G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701198 | |||||||
| chr9:120701381 | T | C | 1 | a0002c0001t0001g0002 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.601+12377A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701381 | |||||||
| chr9:120701610 | A | G | 21 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(18): Show |
21 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.601+12148T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701610 | |||||||
| chr9:120701656 | A | C | 2 | a0001c0002t0014g0199 a0001c0002t0014g0255 |
2 | NA18975.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.601+12102T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701656 | |||||||
| chr9:120701819 | C | T | 2 | a0001c0002t0001g0189 a0002c0001t0001g0065 |
2 | HG03017.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.601+11939G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701819 | |||||||
| chr9:120701823 | T | C | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+11935A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701823 | |||||||
| chr9:120701900 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+11858T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701900 | |||||||
| chr9:120701913 | G | A | 1 | a0001c0003t0018g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.601+11845C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701913 | |||||||
| chr9:120701952 | C | A | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+11806G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701952 | |||||||
| chr9:120701953 | G | A | 1 | a0002c0001t0001g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+11805C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120701953 | |||||||
| chr9:120702008 | T | A | 276 | a0001c0002t0001g0171 a0001c0002t0001g0189 a0001c0002t0002g0164 others(273): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.601+11750A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702008 | |||||||
| chr9:120702043 | T | TA | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+11714dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702043 | |||||||
| chr9:120702055 | T | A | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.601+11703A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702055 | |||||||
| chr9:120702162 | G | A | 5 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+11596C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702162 | |||||||
| chr9:120702163 | G | T | 1 | a0001c0003t0027g0158 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.601+11595C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702163 | |||||||
| chr9:120702167 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+11591G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702167 | |||||||
| chr9:120702173 | T | A | 1 | a0001c0002t0012g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.601+11585A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702173 | |||||||
| chr9:120702184 | A | G | 1 | a0002c0001t0001g0018 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.601+11574T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702184 | |||||||
| chr9:120702310 | A | G | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+11448T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702310 | |||||||
| chr9:120702501 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+11257G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702501 | |||||||
| chr9:120702526 | A | G | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.601+11232T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702526 | |||||||
| chr9:120702737 | G | A | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+11021C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702737 | |||||||
| chr9:120702745 | G | C | 48 | a0001c0002t0001g0171 a0002c0001t0001g0002 a0002c0001t0001g0003 others(45): Show |
48 | HG00408.hp2 HG00673.hp1 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.601+11013C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120702745 | |||||||
| chr9:120703077 | C | T | 2 | a0002c0001t0001g0096 a0002c0001t0001g0097 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.601+10681G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120703077 | |||||||
| chr9:120703088 | T | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+10670A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120703088 | |||||||
| chr9:120703241 | G | T | 11 | a0002c0001t0001g0001 a0002c0001t0001g0015 a0002c0001t0001g0042 others(8): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+10517C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120703241 | |||||||
| chr9:120703491 | A | G | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+10267T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120703491 | |||||||
| chr9:120703610 | G | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+10148C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120703610 | |||||||
| chr9:120703669 | A | G | 23 | a0001c0002t0002g0172 a0001c0002t0002g0191 a0001c0002t0002g0200 others(20): Show |
23 | HG00408.hp1 HG02074.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.601+10089T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120703669 | |||||||
| chr9:120703670 | G | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+10088C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120703670 | |||||||
| chr9:120703940 | T | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+9818A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120703940 | |||||||
| chr9:120704050 | G | C | 138 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(135): Show |
138 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.601+9708C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704050 | |||||||
| chr9:120704059 | C | T | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+9699G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704059 | |||||||
| chr9:120704104 | C | T | 11 | a0002c0001t0001g0001 a0002c0001t0001g0015 a0002c0001t0001g0042 others(8): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+9654G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704104 | |||||||
| chr9:120704109 | G | A | 1 | a0001c0002t0002g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.601+9649C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704109 | |||||||
| chr9:120704227 | G | A | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+9531C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704227 | |||||||
| chr9:120704279 | A | C | 2 | a0001c0002t0002g0248 a0001c0002t0016g0247 |
2 | HG00621.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.601+9479T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704279 | |||||||
| chr9:120704333 | CA | C | 13 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.601+9424delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704333 | |||||||
| chr9:120704782 | T | C | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+8976A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704782 | |||||||
| chr9:120704893 | A | G | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+8865T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704893 | |||||||
| chr9:120704985 | AT | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+8772delA | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120704985 | |||||||
| chr9:120705098 | G | C | 3 | a0002c0001t0001g0123 a0002c0001t0001g0124 a0002c0001t0004g0125 |
3 | NA18959.hp1 NA19078.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.601+8660C>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705098 | |||||||
| chr9:120705292 | C | T | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.601+8466G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705292 | |||||||
| chr9:120705402 | T | C | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+8356A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705402 | |||||||
| chr9:120705482 | G | A | 1 | a0002c0001t0001g0012 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.601+8276C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705482 | |||||||
| chr9:120705492 | T | C | 1 | a0002c0001t0001g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.601+8266A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705492 | |||||||
| chr9:120705517 | T | A | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+8241A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705517 | |||||||
| chr9:120705540 | G | T | 1 | a0001c0002t0002g0174 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.601+8218C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705540 | |||||||
| chr9:120705786 | C | T | 2 | a0002c0001t0001g0043 a0002c0001t0001g0126 |
2 | HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.601+7972G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705786 | |||||||
| chr9:120705837 | T | C | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+7921A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120705837 | |||||||
| chr9:120706016 | G | A | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+7742C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120706016 | |||||||
| chr9:120706020 | T | A | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.601+7738A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120706020 | |||||||
| chr9:120706345 | G | A | 1 | a0001c0003t0005g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.601+7413C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120706345 | |||||||
| chr9:120706668 | C | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+7090G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120706668 | |||||||
| chr9:120706809 | C | T | 117 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(114): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.601+6949G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120706809 | |||||||
| chr9:120707009 | A | G | 1 | a0002c0001t0001g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.601+6749T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707009 | |||||||
| chr9:120707203 | A | G | 1 | a0001c0003t0008g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.601+6555T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707203 | |||||||
| chr9:120707457 | A | G | 1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.601+6301T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707457 | |||||||
| chr9:120707707 | C | G | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+6051G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707707 | |||||||
| chr9:120707768 | C | A | 1 | a0001c0002t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.601+5990G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707768 | |||||||
| chr9:120707846 | C | G | 1 | a0002c0001t0001g0041 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.601+5912G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707846 | |||||||
| chr9:120707858 | C | A | 1 | a0003c0007t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.601+5900G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707858 | |||||||
| chr9:120707976 | C | T | 7 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0002c0001t0001g0036 others(4): Show |
7 | HG02055.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.601+5782G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707976 | |||||||
| chr9:120707992 | C | T | 42 | a0001c0002t0001g0171 a0001c0002t0002g0259 a0001c0002t0006g0258 others(39): Show |
42 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.601+5766G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120707992 | |||||||
| chr9:120708043 | TCAAA | T | 11 | a0001c0003t0003g0141 a0001c0003t0003g0142 a0001c0003t0003g0143 others(8): Show |
11 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.601+5711_601+5714d others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708043 | |||||||
| chr9:120708097 | C | T | 1 | a0001c0002t0002g0257 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.601+5661G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708097 | |||||||
| chr9:120708132 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+5626G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708132 | |||||||
| chr9:120708314 | G | A | 3 | a0002c0001t0001g0107 a0002c0001t0010g0094 a0002c0001t0010g0095 |
3 | HG01099.hp1 HG02055.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.601+5444C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708314 | |||||||
| chr9:120708324 | C | G | 1 | a0002c0001t0001g0017 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.601+5434G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708324 | |||||||
| chr9:120708343 | A | G | 151 | a0001c0002t0001g0189 a0001c0002t0002g0164 a0001c0002t0002g0170 others(148): Show |
151 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.601+5415T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708343 | |||||||
| chr9:120708372 | A | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+5386T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708372 | |||||||
| chr9:120708593 | A | G | 8 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+5165T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708593 | |||||||
| chr9:120708823 | T | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+4935A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708823 | |||||||
| chr9:120708967 | C | T | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+4791G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120708967 | |||||||
| chr9:120709005 | A | G | 2 | a0001c0002t0002g0245 a0001c0002t0002g0246 |
2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.601+4753T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709005 | |||||||
| chr9:120709245 | T | C | 11 | a0001c0002t0002g0186 a0001c0002t0002g0187 a0001c0002t0002g0245 others(8): Show |
11 | HG00558.hp1 HG00621.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.601+4513A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709245 | |||||||
| chr9:120709302 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+4456C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709302 | |||||||
| chr9:120709417 | A | C | 2 | a0002c0001t0001g0003 a0002c0001t0001g0004 |
2 | NA18963.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.601+4341T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709417 | |||||||
| chr9:120709521 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+4237C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709521 | |||||||
| chr9:120709525 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+4233T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709525 | |||||||
| chr9:120709675 | T | C | 1 | a0001c0002t0002g0180 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.601+4083A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709675 | |||||||
| chr9:120709865 | A | G | 1 | a0001c0002t0002g0172 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.601+3893T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709865 | |||||||
| chr9:120709973 | C | T | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+3785G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709973 | |||||||
| chr9:120709974 | G | A | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+3784C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120709974 | |||||||
| chr9:120710027 | C | T | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+3731G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710027 | |||||||
| chr9:120710028 | G | A | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+3730C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710028 | |||||||
| chr9:120710032 | C | CAA | 9 | a0001c0003t0003g0141 a0001c0003t0003g0142 a0001c0003t0003g0144 others(6): Show |
9 | HG00639.hp1 HG01891.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.601+3724_601+3725d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710032 | |||||||
| chr9:120710032 | CA | C | 130 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(127): Show |
130 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.601+3725delT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710032 | |||||||
| chr9:120710079 | C | T | 1 | a0001c0002t0002g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.601+3679G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710079 | |||||||
| chr9:120710262 | T | C | 150 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(147): Show |
150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.601+3496A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710262 | |||||||
| chr9:120710290 | T | C | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+3468A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710290 | |||||||
| chr9:120710373 | G | A | 9 | a0002c0001t0001g0096 a0002c0001t0001g0097 a0002c0001t0001g0098 others(6): Show |
9 | HG01109.hp2 HG01261.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+3385C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710373 | |||||||
| chr9:120710422 | C | A | 1 | a0001c0002t0002g0254 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.601+3336G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710422 | |||||||
| chr9:120710424 | T | TA | 33 | a0001c0002t0002g0183 a0001c0002t0012g0285 a0001c0002t0012g0286 others(30): Show |
33 | HG01099.hp1 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.601+3333dupT | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710424 | |||||||
| chr9:120710424 | T | TAA | 112 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0172 others(109): Show |
112 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.601+3332_601+3333d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710424 | |||||||
| chr9:120710424 | T | TAAA | 7 | a0001c0002t0002g0188 a0001c0002t0002g0197 a0001c0002t0002g0198 others(4): Show |
7 | HG00642.hp1 HG01106.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.601+3331_601+3333d others(5): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710424 | |||||||
| chr9:120710635 | A | G | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+3123T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710635 | |||||||
| chr9:120710896 | T | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+2862A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710896 | |||||||
| chr9:120710964 | G | A | 20 | a0001c0002t0002g0172 a0002c0001t0001g0108 a0002c0001t0001g0109 others(17): Show |
20 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.601+2794C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120710964 | |||||||
| chr9:120711040 | T | C | 1 | a0002c0001t0001g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.601+2718A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711040 | |||||||
| chr9:120711107 | C | T | 21 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 others(18): Show |
21 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.601+2651G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711107 | |||||||
| chr9:120711138 | G | A | 116 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0173 others(113): Show |
116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.601+2620C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711138 | |||||||
| chr9:120711266 | T | G | 3 | a0001c0002t0002g0272 a0001c0002t0002g0273 a0001c0002t0002g0274 |
3 | HG02040.hp2 NA18949.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.601+2492A>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711266 | |||||||
| chr9:120711325 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+2433A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711325 | |||||||
| chr9:120711586 | T | C | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+2172A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711586 | |||||||
| chr9:120711656 | A | G | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+2102T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711656 | |||||||
| chr9:120711772 | T | C | 115 | a0001c0002t0002g0164 a0001c0002t0002g0170 a0001c0002t0002g0173 others(112): Show |
115 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.601+1986A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711772 | |||||||
| chr9:120711829 | C | A | 7 | a0001c0003t0008g0150 a0001c0003t0008g0151 a0001c0003t0008g0152 others(4): Show |
7 | HG02809.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+1929G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711829 | |||||||
| chr9:120711831 | A | G | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+1927T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711831 | |||||||
| chr9:120711836 | T | TAC | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+1920_601+1921d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711836 | |||||||
| chr9:120711840 | T | C | 16 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+1918A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | T | TAC | 8 | a0001c0002t0002g0174 a0001c0002t0002g0175 a0001c0002t0002g0176 others(5): Show |
8 | HG00597.hp1 HG00673.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+1916_601+1917d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | T | TACAC | 7 | a0001c0002t0002g0182 a0001c0002t0002g0183 a0001c0002t0002g0184 others(4): Show |
7 | HG01358.hp1 HG01975.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.601+1917_601+1918i others(6): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | T | TACACAC | 12 | a0001c0002t0002g0190 a0001c0002t0002g0191 a0001c0002t0002g0192 others(9): Show |
12 | HG00323.hp2 HG00438.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+1917_601+1918i others(8): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | T | TACACACA others(1): Show |
61 | a0001c0002t0002g0164 a0001c0002t0002g0200 a0001c0002t0002g0201 others(58): Show |
61 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.601+1917_601+1918i others(10): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | T | TACACACA others(3): Show |
19 | a0001c0002t0002g0257 a0001c0002t0002g0259 a0001c0002t0002g0260 others(16): Show |
19 | HG00609.hp2 HG01261.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.601+1917_601+1918i others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | T | TACACACA others(5): Show |
1 | a0001c0002t0002g0275 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.601+1917_601+1918i others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | T | TACACACA others(7): Show |
2 | a0001c0002t0002g0276 a0001c0002t0002g0277 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.601+1917_601+1918i others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | T | TACACACA others(9): Show |
6 | a0001c0002t0002g0278 a0001c0002t0002g0279 a0001c0002t0002g0281 others(3): Show |
6 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+1917_601+1918i others(18): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711840 | TACATACA others(13): Show |
T | 1 | a0001c0002t0002g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.601+1898_601+1917d others(22): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711840 | |||||||
| chr9:120711844 | T | C | 135 | a0001c0002t0002g0164 a0001c0002t0002g0174 a0001c0002t0002g0175 others(132): Show |
135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.601+1914A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711844 | |||||||
| chr9:120711844 | T | TAC | 4 | a0002c0001t0001g0127 a0002c0001t0001g0128 a0002c0001t0001g0129 others(1): Show |
4 | HG02630.hp2 HG04115.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+1912_601+1913d others(4): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711844 | |||||||
| chr9:120711844 | T | TACACACA others(1): Show |
4 | a0001c0002t0001g0189 a0001c0003t0008g0151 a0001c0003t0008g0152 others(1): Show |
4 | HG03041.hp1 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+1906_601+1913d others(10): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711844 | |||||||
| chr9:120711844 | T | TACACACA others(5): Show |
3 | a0001c0003t0011g0154 a0001c0003t0011g0155 a0001c0003t0011g0156 |
3 | HG02809.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.601+1902_601+1913d others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711844 | |||||||
| chr9:120711844 | T | TACATACA others(5): Show |
1 | a0001c0003t0008g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.601+1913_601+1914i others(14): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711844 | |||||||
| chr9:120711844 | T | TACATACA others(7): Show |
3 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 |
3 | HG02965.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.601+1913_601+1914i others(16): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711844 | |||||||
| chr9:120711844 | T | TACATACA others(9): Show |
2 | a0001c0004t0005g0168 a0001c0010t0005g0169 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.601+1913_601+1914i others(18): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711844 | |||||||
| chr9:120711869 | A | C | 1 | a0001c0003t0008g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.601+1889T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711869 | |||||||
| chr9:120711871 | A | ACACAC | 5 | a0001c0003t0003g0143 a0001c0003t0003g0144 a0001c0003t0003g0145 others(2): Show |
5 | HG00639.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+1886_601+1887i others(7): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711871 | |||||||
| chr9:120711871 | A | ACACACAC others(4): Show |
1 | a0001c0003t0003g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.601+1886_601+1887i others(13): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711871 | |||||||
| chr9:120711871 | A | ACACACAC others(19): Show |
1 | a0001c0002t0012g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.601+1886_601+1887i others(28): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711871 | |||||||
| chr9:120711871 | A | ACACACAC others(11): Show |
1 | a0001c0002t0012g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.601+1886_601+1887i others(20): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711871 | |||||||
| chr9:120711871 | A | ACACACAC others(9): Show |
1 | a0001c0002t0012g0285 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.601+1886_601+1887i others(18): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711871 | |||||||
| chr9:120711871 | A | ACACACAC others(2): Show |
3 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 |
3 | HG01891.hp1 HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.601+1886_601+1887i others(11): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711871 | |||||||
| chr9:120711871 | A | ACACACAC others(3): Show |
1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+1886_601+1887i others(12): Show |
MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711871 | |||||||
| chr9:120711871 | A | C | 1 | a0002c0001t0001g0013 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.601+1887T>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711871 | |||||||
| chr9:120711873 | C | A | 2 | a0001c0002t0015g0288 a0001c0002t0015g0289 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.601+1885G>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711873 | |||||||
| chr9:120711966 | T | A | 3 | a0002c0001t0001g0134 a0002c0001t0001g0135 a0002c0001t0001g0136 |
3 | HG02109.hp2 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.601+1792A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120711966 | |||||||
| chr9:120712130 | C | T | 1 | a0001c0003t0017g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+1628G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120712130 | |||||||
| chr9:120712353 | A | G | 3 | a0001c0002t0012g0285 a0001c0002t0012g0286 a0001c0002t0012g0287 |
3 | HG02615.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+1405T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120712353 | |||||||
| chr9:120712514 | T | A | 1 | a0001c0003t0019g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601+1244A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120712514 | |||||||
| chr9:120712517 | A | G | 11 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(8): Show |
11 | HG02040.hp1 HG02523.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.601+1241T>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120712517 | |||||||
| chr9:120712774 | C | G | 5 | a0001c0004t0005g0165 a0001c0004t0005g0166 a0001c0004t0005g0167 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+984G>C | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120712774 | |||||||
| chr9:120712904 | T | C | 12 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+854A>G | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120712904 | |||||||
| chr9:120713085 | G | T | 1 | a0001c0002t0002g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.601+673C>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120713085 | |||||||
| chr9:120713112 | T | A | 1 | a0002c0001t0001g0137 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.601+646A>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120713112 | |||||||
| chr9:120713569 | G | A | 1 | a0001c0002t0002g0284 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.601+189C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120713569 | |||||||
| chr9:120713614 | G | A | 1 | a0002c0001t0002g0138 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.601+144C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120713614 | |||||||
| chr9:120713615 | C | T | 9 | a0001c0003t0003g0140 a0001c0003t0003g0141 a0001c0003t0003g0142 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.601+143G>A | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120713615 | |||||||
| chr9:120713737 | G | A | 3 | a0001c0003t0005g0160 a0001c0003t0005g0161 a0001c0003t0005g0162 |
3 | HG02572.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601+21C>T | MEGF9 | ENSG00000106780.9 | transcript | ENST00000373930.4 | protein_coding | 1/5 | chr9 | 120713737 |