Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54531 |
| ensemblid | ENSG00000105556.12 |
| hgncid | 29210 |
| symbol | MIER2 |
| name | MIER family member 2 |
| refseq_nuc | NM_017550.3 |
| refseq_prot | NP_060020.1 |
| ensembl_nuc | ENST00000264819.7 |
| ensembl_prot | ENSP00000264819.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 305573 |
| end | 344796 |
| strand | - |
| ver | v1.2 |
| region | chr19:305573-344796 |
| region5000 | chr19:300573-349796 |
| regionname0 | MIER2_chr19_305573_344796 |
| regionname5000 | MIER2_chr19_300573_349796 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 545 | 364 | 77 | 79 | 146 | 15 | 45 | 106 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| a0002 | 0/0 | 545 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| a0003 | 0/0 | 545 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| a0004 | 0/0 | 545 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| a0005 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| a0006 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| a0007 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| a0008 | 0/0 | 545 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| a0009 | 0/0 | 545 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | MAEAS others(540): Show |
chr19 | 300573 | 349796 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1635 | 288 | 40 | 60 | 130 | 14 | 42 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0002 | 0/0 | 1635 | 23 | 14 | 7 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0003 | 0/0 | 1635 | 15 | 0 | 6 | 9 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0005 | 0/0 | 1635 | 8 | 8 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0006 | 0/0 | 1635 | 5 | 4 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0007 | 0/0 | 1635 | 4 | 4 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0008 | 0/0 | 1635 | 4 | 0 | 0 | 4 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0009 | 0/0 | 1635 | 3 | 2 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0010 | 0/0 | 1635 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0011 | 0/0 | 1635 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0013 | 0/0 | 1635 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0014 | 0/0 | 1635 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0017 | 0/0 | 1635 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0021 | 0/0 | 1635 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0022 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0023 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0024 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0001c0027 | 0/0 | 1635 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0002c0004 | 0/0 | 1635 | 10 | 10 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0002c0015 | 0/0 | 1635 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0003c0012 | 0/0 | 1635 | 2 | 1 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0004c0019 | 0/0 | 1635 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0005c0025 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0006c0018 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0007c0020 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0008c0016 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 | ||
| a0009c0026 | 0/0 | 1635 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | ATGGC others(1630): Show |
chr19 | 300573 | 349796 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2769 | 270 | 31 | 59 | 124 | 14 | 40 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0001t0002 | 0/0 | 2769 | 3 | 2 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0001t0004 | 0/0 | 2769 | 5 | 5 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0001t0005 | 0/0 | 2769 | 5 | 0 | 0 | 4 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0001t0007 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0001t0008 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0001t0011 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0001t0012 | 0/0 | 2769 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0001t0013 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0002t0001 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0002t0002 | 0/0 | 2769 | 22 | 13 | 7 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0003t0002 | 0/0 | 2769 | 15 | 0 | 6 | 9 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0005t0002 | 0/0 | 2769 | 8 | 8 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0006t0001 | 0/0 | 2769 | 4 | 3 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0006t0003 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0007t0001 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0007t0006 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0007t0009 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0008t0001 | 0/0 | 2769 | 4 | 0 | 0 | 4 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0009t0001 | 0/0 | 2769 | 3 | 2 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0010t0001 | 0/0 | 2769 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0011t0002 | 0/0 | 2769 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0013t0001 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0014t0002 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0017t0001 | 0/0 | 2769 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0021t0014 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0022t0002 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0023t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0024t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0001c0027t0001 | 0/0 | 2769 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0002c0004t0003 | 0/0 | 2769 | 10 | 10 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0002c0015t0003 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0003c0012t0001 | 0/0 | 2769 | 2 | 1 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0004c0019t0001 | 0/0 | 2769 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0005c0025t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0006c0018t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0007c0020t0010 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0008c0016t0001 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| a0009c0026t0002 | 0/0 | 2769 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | GCGCA others(2764): Show |
chr19 | 300573 | 349796 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 5 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0005g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0011g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0012g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0001t0013g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0005t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0005t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0005t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0005t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0005t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0005t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0006t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0006t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0007t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0007t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0007t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0007t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0008t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0008t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0008t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0008t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0009t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0009t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0009t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0010t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0011t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0011t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0013t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0013t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0014t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0014t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0017t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0021t0014g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0022t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0023t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0024t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0001c0027t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0004t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0015t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0002c0015t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0003c0012t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0003c0012t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0004c0019t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0005c0025t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0006c0018t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0007c0020t0010g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0008c0016t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| a0009c0026t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0017 | t0001 | g0097 | EUR | GBR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | FIN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0192 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00597 | hp1 | a0001 | c0023 | t0001 | g0219 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00735 | hp2 | a0001 | c0011 | t0002 | g0283 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0158 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0153 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01109 | hp2 | a0001 | c0011 | t0002 | g0267 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01175 | hp1 | a0001 | c0009 | t0001 | g0077 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0122 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0121 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0241 | AMR | PUR | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01256 | hp1 | a0001 | c0010 | t0001 | g0017 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01258 | hp2 | a0001 | c0010 | t0001 | g0017 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01346 | hp1 | a0001 | c0027 | t0001 | g0160 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0163 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01496 | hp1 | a0004 | c0019 | t0001 | g0203 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01884 | hp2 | a0001 | c0005 | t0002 | g0245 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01891 | hp1 | a0001 | c0005 | t0002 | g0129 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0110 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0119 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02004 | hp2 | a0001 | c0003 | t0002 | g0161 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02055 | hp1 | a0002 | c0015 | t0003 | g0242 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02055 | hp2 | a0001 | c0006 | t0003 | g0141 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0124 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02257 | hp2 | a0002 | c0004 | t0003 | g0143 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02258 | hp2 | a0002 | c0004 | t0003 | g0106 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02273 | hp2 | a0001 | c0003 | t0002 | g0155 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0162 | AMR | PEL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0137 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02523 | hp1 | a0001 | c0001 | t0011 | g0265 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02615 | hp1 | a0002 | c0004 | t0003 | g0134 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0120 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02647 | hp1 | a0001 | c0006 | t0001 | g0014 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02647 | hp2 | a0001 | c0001 | t0013 | g0313 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02717 | hp1 | a0002 | c0004 | t0003 | g0142 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0175 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02723 | hp2 | a0001 | c0007 | t0006 | g0171 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0246 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0123 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02895 | hp1 | a0001 | c0005 | t0002 | g0244 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02895 | hp2 | a0001 | c0009 | t0001 | g0062 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02897 | hp2 | a0001 | c0009 | t0001 | g0042 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02965 | hp1 | a0001 | c0021 | t0014 | g0108 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0111 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0092 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02976 | hp2 | a0001 | c0013 | t0001 | g0258 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03041 | hp2 | a0002 | c0015 | t0003 | g0247 | AFR | GWD | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03139 | hp1 | a0002 | c0004 | t0003 | g0135 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03195 | hp2 | a0001 | c0014 | t0002 | g0032 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0131 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03225 | hp1 | a0002 | c0004 | t0003 | g0133 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03225 | hp2 | a0001 | c0005 | t0002 | g0013 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03453 | hp1 | a0001 | c0005 | t0002 | g0013 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03486 | hp1 | a0001 | c0007 | t0009 | g0170 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03486 | hp2 | a0001 | c0005 | t0002 | g0130 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | ESN | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03579 | hp1 | a0001 | c0006 | t0001 | g0014 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03579 | hp2 | a0002 | c0004 | t0003 | g0138 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03654 | hp2 | a0003 | c0012 | t0001 | g0048 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0063 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0113 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG04184 | hp2 | a0001 | c0006 | t0001 | g0084 | SAS | BEB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG04199 | hp1 | a0001 | c0001 | t0012 | g0071 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0118 | AFR | YRI | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18941 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18948 | hp2 | a0001 | c0024 | t0001 | g0194 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18951 | hp2 | a0001 | c0003 | t0002 | g0185 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0152 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18971 | hp1 | a0005 | c0025 | t0001 | g0184 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0159 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18975 | hp2 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18989 | hp2 | a0001 | c0008 | t0001 | g0075 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18990 | hp2 | a0001 | c0008 | t0001 | g0202 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18992 | hp1 | a0006 | c0018 | t0001 | g0198 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18992 | hp2 | a0001 | c0003 | t0002 | g0156 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18994 | hp1 | a0001 | c0022 | t0002 | g0326 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18995 | hp2 | a0001 | c0003 | t0002 | g0015 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19002 | hp2 | a0007 | c0020 | t0010 | g0050 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19030 | hp1 | a0002 | c0004 | t0003 | g0140 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19043 | hp1 | a0002 | c0004 | t0003 | g0136 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19077 | hp2 | a0008 | c0016 | t0001 | g0195 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19081 | hp2 | a0001 | c0003 | t0002 | g0157 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19084 | hp1 | a0001 | c0008 | t0001 | g0049 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19090 | hp1 | a0001 | c0008 | t0001 | g0068 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0151 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ASW | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ASW | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA20752 | hp2 | a0009 | c0026 | t0002 | g0128 | EUR | TSI | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | GIH | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | GIH | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02109 | hp1 | a0001 | c0014 | t0002 | g0033 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02486 | hp1 | a0001 | c0005 | t0002 | g0132 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02486 | hp2 | a0002 | c0004 | t0003 | g0139 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0240 | AFR | ACB | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03471 | hp1 | a0001 | c0013 | t0001 | g0257 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | USA | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA20300 | hp2 | a0001 | c0007 | t0001 | g0174 | AFR | USA | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA21309 | hp1 | a0003 | c0012 | t0001 | g0060 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0085 | REF | REF | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0070 | REF | REF | MIER2_chr19_300573_349796 | MIER2 | chr19 | 300573 | 349796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:307282 | T | C | 1 | a0002 | 12 | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
missense_variant | MODERATE | c.1453A>G | p.Ser485Gly | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1467/2769 | 1453/1638 | 485/545 | chr19 | 307282 | |||
| chr19:307345 | G | A | 1 | a0004 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1390C>T | p.Pro464Ser | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1404/2769 | 1390/1638 | 464/545 | chr19 | 307345 | |||
| chr19:307515 | G | A | 1 | a0003 | 2 | HG03654.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.1220C>T | p.Thr407Met | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1234/2769 | 1220/1638 | 407/545 | chr19 | 307515 | |||
| chr19:308602 | T | G | 1 | a0007 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1173A>C | p.Gln391His | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/14 | 1187/2769 | 1173/1638 | 391/545 | chr19 | 308602 | |||
| chr19:308612 | C | T | 1 | a0006 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.1163G>A | p.Arg388His | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/14 | 1177/2769 | 1163/1638 | 388/545 | chr19 | 308612 | |||
| chr19:325700 | A | T | 1 | a0008 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.590T>A | p.Ile197Asn | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/14 | 604/2769 | 590/1638 | 197/545 | chr19 | 325700 | |||
| chr19:327157 | C | G | 1 | a0009 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.469G>C | p.Asp157His | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/14 | 483/2769 | 469/1638 | 157/545 | chr19 | 327157 | |||
| chr19:334446 | C | A | 1 | a0005 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.197G>T | p.Cys66Phe | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/14 | 211/2769 | 197/1638 | 66/545 | chr19 | 334446 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:307145 | G | A | 3 | a0001c0003 a0001c0011 a0001c0022 |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
synonymous_variant | LOW | c.1590C>T | p.Pro530Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1604/2769 | 1590/1638 | 530/545 | chr19 | 307145 | |||
| chr19:307349 | C | T | 1 | a0001c0007 | 4 | HG02717.hp2 HG02723.hp2 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.1386G>A | p.Pro462Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1400/2769 | 1386/1638 | 462/545 | chr19 | 307349 | |||
| chr19:307526 | G | A | 1 | a0001c0013 | 2 | HG02976.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.1209C>T | p.Ser403Ser | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/14 | 1223/2769 | 1209/1638 | 403/545 | chr19 | 307526 | |||
| chr19:308623 | G | T | 1 | a0001c0017 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1152C>A | p.Pro384Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/14 | 1166/2769 | 1152/1638 | 384/545 | chr19 | 308623 | |||
| chr19:308662 | G | A | 1 | a0001c0008 | 4 | NA18989.hp2 NA18990.hp2 NA19084.hp1 others(1): Show |
synonymous_variant | LOW | c.1113C>T | p.Asp371Asp | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/14 | 1127/2769 | 1113/1638 | 371/545 | chr19 | 308662 | |||
| chr19:311911 | C | T | 1 | a0001c0010 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.918G>A | p.Glu306Glu | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/14 | 932/2769 | 918/1638 | 306/545 | chr19 | 311911 | |||
| chr19:313633 | G | A | 5 | a0001c0003 a0001c0005 a0001c0014 others(2): Show |
27 | HG01071.hp2 HG01106.hp1 HG01361.hp2 others(24): Show |
synonymous_variant | LOW | c.666C>T | p.Asn222Asn | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/14 | 680/2769 | 666/1638 | 222/545 | chr19 | 313633 | |||
| chr19:326522 | G | A | 1 | a0001c0023 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.570C>T | p.Ala190Ala | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/14 | 584/2769 | 570/1638 | 190/545 | chr19 | 326522 | |||
| chr19:327167 | G | A | 1 | a0001c0014 | 2 | HG02109.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.459C>T | p.His153His | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/14 | 473/2769 | 459/1638 | 153/545 | chr19 | 327167 | |||
| chr19:327182 | C | T | 7 | a0001c0002 a0001c0003 a0001c0005 others(4): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
synonymous_variant | LOW | c.444G>A | p.Pro148Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/14 | 458/2769 | 444/1638 | 148/545 | chr19 | 327182 | |||
| chr19:327900 | G | A | 2 | a0001c0003 a0001c0027 |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
synonymous_variant | LOW | c.333C>T | p.Asp111Asp | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/14 | 347/2769 | 333/1638 | 111/545 | chr19 | 327900 | |||
| chr19:327939 | C | T | 1 | a0001c0014 | 2 | HG02109.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.294G>A | p.Ala98Ala | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/14 | 308/2769 | 294/1638 | 98/545 | chr19 | 327939 | |||
| chr19:327945 | G | A | 1 | a0001c0024 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.288C>T | p.Tyr96Tyr | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/14 | 302/2769 | 288/1638 | 96/545 | chr19 | 327945 | |||
| chr19:334474 | T | G | 9 | a0001c0002 a0001c0003 a0001c0005 others(6): Show |
67 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(64): Show |
synonymous_variant | LOW | c.169A>C | p.Arg57Arg | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/14 | 183/2769 | 169/1638 | 57/545 | chr19 | 334474 | |||
| chr19:336102 | C | T | 1 | a0001c0009 | 3 | HG01175.hp1 HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.81G>A | p.Pro27Pro | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/14 | 95/2769 | 81/1638 | 27/545 | chr19 | 336102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:305602 | A | C | 1 | a0007c0020t0010 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1088T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 1088 | chr19 | 305602 | ||||||
| chr19:305684 | A | C | 1 | a0007c0020t0010 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1006T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 1006 | chr19 | 305684 | ||||||
| chr19:305759 | C | T | 2 | a0001c0007t0006 a0001c0007t0009 |
2 | HG02723.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*931G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 931 | chr19 | 305759 | ||||||
| chr19:305762 | G | A | 1 | a0001c0001t0011 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*928C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 928 | chr19 | 305762 | ||||||
| chr19:305903 | A | C | 1 | a0001c0001t0004 | 5 | HG02258.hp1 HG02896.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*787T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 787 | chr19 | 305903 | ||||||
| chr19:305910 | G | A | 1 | a0001c0001t0005 | 5 | HG03669.hp2 NA18950.hp1 NA18964.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*780C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 780 | chr19 | 305910 | ||||||
| chr19:305938 | C | G | 1 | a0001c0001t0008 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 752 | chr19 | 305938 | ||||||
| chr19:305939 | C | T | 1 | a0001c0001t0007 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*751G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 751 | chr19 | 305939 | ||||||
| chr19:305940 | G | A | 1 | a0001c0001t0012 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 750 | chr19 | 305940 | ||||||
| chr19:306304 | C | T | 12 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0013 others(9): Show |
62 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*386G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 386 | chr19 | 306304 | ||||||
| chr19:306318 | G | A | 1 | a0001c0001t0013 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 372 | chr19 | 306318 | ||||||
| chr19:306320 | G | C | 1 | a0001c0021t0014 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*370C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 370 | chr19 | 306320 | ||||||
| chr19:306329 | G | A | 3 | a0001c0006t0003 a0002c0004t0003 a0002c0015t0003 |
13 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 14/14 | 361 | chr19 | 306329 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:306753 | C | T | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1617-42G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/13 | chr19 | 306753 | |||||||
| chr19:306819 | C | G | 4 | a0001c0002t0002g0117 a0001c0002t0002g0118 a0001c0002t0002g0120 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1617-108G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/13 | chr19 | 306819 | |||||||
| chr19:307032 | T | C | 4 | a0001c0001t0001g0214 a0001c0008t0001g0049 a0001c0008t0001g0068 others(1): Show |
4 | NA18977.hp2 NA18989.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+87A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/13 | chr19 | 307032 | |||||||
| chr19:307037 | C | T | 48 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(45): Show |
51 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1616+82G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 13/13 | chr19 | 307037 | |||||||
| chr19:307582 | G | A | 1 | a0001c0008t0001g0049 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1199-46C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307582 | |||||||
| chr19:307662 | A | C | 1 | a0007c0020t0010g0050 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1199-126T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307662 | |||||||
| chr19:307767 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1199-231T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307767 | |||||||
| chr19:307791 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1199-255A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307791 | |||||||
| chr19:307796 | A | ATAGGTGT others(57): Show |
17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1199-324_1199-261d others(66): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307796 | |||||||
| chr19:307796 | A | ATAGGTGT others(189): Show |
1 | a0001c0001t0001g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1199-261_1199-260i others(198): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307796 | |||||||
| chr19:307796 | A | ATAGGTGT others(57): Show |
1 | a0001c0021t0014g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1199-261_1199-260i others(66): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307796 | |||||||
| chr19:307820 | A | ACTGCAGA others(61): Show |
30 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0007g0092 others(27): Show |
32 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1199-285_1199-284i others(70): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307820 | |||||||
| chr19:307820 | A | ACTGCAGA others(125): Show |
2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1199-285_1199-284i others(134): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307820 | |||||||
| chr19:307820 | A | ACTGCAGA others(57): Show |
19 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(16): Show |
19 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1199-348_1199-285d others(66): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307820 | |||||||
| chr19:307820 | A | G | 1 | a0001c0021t0014g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1199-284T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307820 | |||||||
| chr19:307828 | G | A | 1 | a0001c0001t0012g0071 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1199-292C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307828 | |||||||
| chr19:307829 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1199-293C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307829 | |||||||
| chr19:307834 | A | T | 1 | a0007c0020t0010g0050 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1199-298T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307834 | |||||||
| chr19:307846 | T | G | 1 | a0007c0020t0010g0050 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1199-310A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307846 | |||||||
| chr19:307884 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1199-348C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307884 | |||||||
| chr19:307926 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1199-390G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 307926 | |||||||
| chr19:308025 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1199-489C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308025 | |||||||
| chr19:308045 | T | C | 9 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1199-509A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308045 | |||||||
| chr19:308092 | C | T | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1198+485G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308092 | |||||||
| chr19:308317 | C | T | 9 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1198+260G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308317 | |||||||
| chr19:308337 | G | A | 18 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(15): Show |
19 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1198+240C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308337 | |||||||
| chr19:308352 | C | T | 1 | a0001c0001t0004g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1198+225G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308352 | |||||||
| chr19:308456 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1198+121G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 12/13 | chr19 | 308456 | |||||||
| chr19:308681 | G | A | 14 | a0001c0002t0002g0109 a0001c0006t0003g0141 a0002c0004t0003g0106 others(11): Show |
14 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110-16C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 11/13 | chr19 | 308681 | |||||||
| chr19:308737 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1109+64C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 11/13 | chr19 | 308737 | |||||||
| chr19:308742 | C | T | 14 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(11): Show |
15 | HG01071.hp2 HG01106.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.1109+59G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 11/13 | chr19 | 308742 | |||||||
| chr19:308935 | G | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
4 | HG00438.hp1 HG02080.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-10C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 308935 | |||||||
| chr19:309012 | G | A | 1 | a0004c0019t0001g0203 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.985-87C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309012 | |||||||
| chr19:309026 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.985-101C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309026 | |||||||
| chr19:309122 | G | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0007g0092 others(2): Show |
5 | HG02109.hp1 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.985-197C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309122 | |||||||
| chr19:309135 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.985-210T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309135 | |||||||
| chr19:309220 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.985-295C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309220 | |||||||
| chr19:309275 | C | T | 48 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(45): Show |
51 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.985-350G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309275 | |||||||
| chr19:309380 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.985-455C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309380 | |||||||
| chr19:309399 | C | A | 2 | a0001c0002t0002g0114 a0001c0002t0002g0115 |
2 | HG02300.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.985-474G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309399 | |||||||
| chr19:309445 | G | A | 57 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(54): Show |
60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-520C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309445 | |||||||
| chr19:309476 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(212): Show |
242 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.985-551T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309476 | |||||||
| chr19:309502 | C | T | 57 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(54): Show |
60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-577G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309502 | |||||||
| chr19:309518 | G | A | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-593C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309518 | |||||||
| chr19:309536 | A | C | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.985-611T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309536 | |||||||
| chr19:309544 | T | C | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-619A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309544 | |||||||
| chr19:309573 | GAC | G | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-650_985-649del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309573 | |||||||
| chr19:309573 | GACACACA others(79): Show |
G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0053 |
2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.985-734_985-649del others(86): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309573 | |||||||
| chr19:309588 | A | ACACAAGG others(238): Show |
7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-664_985-663ins others(245): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309588 | |||||||
| chr19:309617 | G | GACAC | 48 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(45): Show |
51 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.985-696_985-693dup others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309617 | |||||||
| chr19:309657 | GAC | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(171): Show |
199 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.985-734_985-733del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309657 | |||||||
| chr19:309657 | GACAC | G | 6 | a0001c0001t0001g0330 a0001c0002t0002g0243 a0001c0005t0002g0244 others(3): Show |
6 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.985-736_985-733del others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309657 | |||||||
| chr19:309657 | GACACAC | G | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.985-738_985-733del others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309657 | |||||||
| chr19:309661 | C | CACACACA others(366): Show |
7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-737_985-736ins others(373): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309661 | |||||||
| chr19:309674 | A | G | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-749T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309674 | |||||||
| chr19:309674 | ACACACAA others(327): Show |
A | 1 | a0001c0001t0001g0165 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.985-1083_985-750de others(1): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309674 | |||||||
| chr19:309687 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.985-762G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309687 | |||||||
| chr19:309691 | G | T | 29 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(26): Show |
31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.985-766C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309691 | |||||||
| chr19:309703 | G | GAC | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(149): Show |
175 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.985-780_985-779dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309703 | |||||||
| chr19:309703 | G | GACAC | 20 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(17): Show |
21 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.985-782_985-779dup others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309703 | |||||||
| chr19:309703 | G | GACACAC | 30 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(27): Show |
32 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.985-784_985-779dup others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309703 | |||||||
| chr19:309714 | G | A | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-789C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309714 | |||||||
| chr19:309733 | C | G | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-808G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309733 | |||||||
| chr19:309743 | G | GAC | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-820_985-819dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309743 | |||||||
| chr19:309785 | GACAC | G | 49 | a0001c0001t0001g0315 a0001c0001t0002g0023 a0001c0001t0002g0169 others(46): Show |
52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.985-864_985-861del others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309785 | |||||||
| chr19:309798 | A | ATG | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-874_985-873ins others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309798 | |||||||
| chr19:309798 | A | G | 49 | a0001c0001t0001g0199 a0001c0001t0002g0023 a0001c0001t0002g0169 others(46): Show |
52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.985-873T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309798 | |||||||
| chr19:309819 | C | T | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.985-894G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309819 | |||||||
| chr19:309827 | GAC | G | 49 | a0001c0001t0001g0200 a0001c0001t0002g0023 a0001c0001t0002g0169 others(46): Show |
52 | HG00621.hp1 HG00735.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.985-904_985-903del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309827 | |||||||
| chr19:309829 | C | CACACACG others(29): Show |
2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.985-905_985-904ins others(36): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309829 | |||||||
| chr19:309847 | CA | C | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-923delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309847 | |||||||
| chr19:309866 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.985-941C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309866 | |||||||
| chr19:309871 | G | GAC | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.985-948_985-947dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309871 | |||||||
| chr19:309871 | G | GACACACA others(194): Show |
6 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.985-947_985-946ins others(201): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309871 | |||||||
| chr19:309871 | G | GACACACA others(150): Show |
1 | a0001c0021t0014g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985-947_985-946ins others(157): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309871 | |||||||
| chr19:309871 | G | GACACACA others(245): Show |
1 | a0001c0001t0005g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.985-947_985-946ins others(252): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309871 | |||||||
| chr19:309899 | C | G | 57 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(54): Show |
60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-974G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309899 | |||||||
| chr19:309909 | GAC | G | 31 | a0001c0001t0001g0102 a0001c0001t0001g0296 a0001c0001t0002g0023 others(28): Show |
33 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.985-986_985-985del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309909 | |||||||
| chr19:309943 | G | C | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-1018C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309943 | |||||||
| chr19:309950 | A | AGG | 12 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(9): Show |
13 | HG01891.hp1 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.985-1026_985-1025i others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309950 | |||||||
| chr19:309951 | G | GGGAC | 45 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(42): Show |
47 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.985-1027_985-1026i others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309951 | |||||||
| chr19:309953 | G | C | 57 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(54): Show |
60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-1028C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309953 | |||||||
| chr19:309953 | GACACACA others(37): Show |
G | 1 | a0001c0001t0001g0199 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.985-1072_985-1029d others(46): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309953 | |||||||
| chr19:309964 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.985-1039C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309964 | |||||||
| chr19:309980 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.985-1055C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309980 | |||||||
| chr19:309985 | C | T | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.985-1060G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309985 | |||||||
| chr19:309993 | GAC | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0002t0002g0113 others(1): Show |
5 | HG01978.hp1 HG04115.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.985-1070_985-1069d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 309993 | |||||||
| chr19:310007 | C | T | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-1082G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310007 | |||||||
| chr19:310037 | GAC | G | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-1114_985-1113d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310037 | |||||||
| chr19:310051 | C | T | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.985-1126G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310051 | |||||||
| chr19:310052 | G | GCACACAG others(1848): Show |
1 | a0001c0001t0004g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.985-1128_985-1127i others(1857): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | |||||||
| chr19:310052 | G | GCACACAG others(1890): Show |
1 | a0001c0001t0004g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.985-1128_985-1127i others(1899): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | |||||||
| chr19:310052 | G | GCACACAG others(1892): Show |
3 | a0001c0001t0004g0073 a0001c0001t0004g0255 a0001c0002t0002g0125 |
3 | HG02258.hp1 HG02896.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.985-1128_985-1127i others(1901): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | |||||||
| chr19:310052 | G | GCACACAG others(1888): Show |
1 | a0001c0021t0014g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985-1128_985-1127i others(1897): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | |||||||
| chr19:310052 | G | GCACACAG others(1886): Show |
1 | a0001c0001t0004g0253 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.985-1128_985-1127i others(1895): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310052 | |||||||
| chr19:310071 | C | G | 57 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(54): Show |
60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-1146G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310071 | |||||||
| chr19:310074 | G | A | 1 | a0001c0021t0014g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985-1149C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310074 | |||||||
| chr19:310096 | T | C | 57 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(54): Show |
60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.985-1171A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310096 | |||||||
| chr19:310103 | T | C | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-1178A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310103 | |||||||
| chr19:310160 | C | T | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0288 others(1): Show |
4 | NA18950.hp2 NA18965.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.985-1235G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310160 | |||||||
| chr19:310161 | G | A | 2 | a0001c0001t0004g0061 a0001c0001t0004g0073 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.985-1236C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310161 | |||||||
| chr19:310213 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.985-1288C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310213 | |||||||
| chr19:310283 | A | G | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-1358T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310283 | |||||||
| chr19:310310 | G | T | 1 | a0001c0001t0004g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.985-1385C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310310 | |||||||
| chr19:310369 | C | T | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.985-1444G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310369 | |||||||
| chr19:310381 | T | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG00642.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.985-1456A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310381 | |||||||
| chr19:310404 | A | G | 31 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(28): Show |
32 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.984+1441T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310404 | |||||||
| chr19:310504 | T | C | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.984+1341A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310504 | |||||||
| chr19:310508 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0223 a0006c0018t0001g0198 |
3 | NA18967.hp2 NA18992.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.984+1337T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310508 | |||||||
| chr19:310514 | C | T | 1 | a0001c0002t0002g0122 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.984+1331G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310514 | |||||||
| chr19:310520 | TGAGCTAT others(35): Show |
T | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.984+1283_984+1324d others(44): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310520 | |||||||
| chr19:310547 | G | GCAGAAAC others(217): Show |
1 | a0001c0002t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.984+1297_984+1298i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310547 | |||||||
| chr19:310557 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.984+1288C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(94): Show |
1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.984+1287_984+1288i others(103): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(196): Show |
1 | a0001c0001t0002g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.984+1287_984+1288i others(205): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(196): Show |
47 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(44): Show |
49 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.984+1287_984+1288i others(205): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(195): Show |
1 | a0001c0002t0002g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.984+1287_984+1288i others(204): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(218): Show |
1 | a0001c0001t0001g0230 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.984+1287_984+1288i others(227): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(217): Show |
14 | a0001c0001t0001g0005 a0001c0001t0001g0087 a0001c0001t0001g0088 others(11): Show |
16 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.984+1287_984+1288i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(217): Show |
1 | a0001c0001t0001g0199 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.984+1287_984+1288i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(217): Show |
146 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(143): Show |
169 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.984+1287_984+1288i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(217): Show |
1 | a0001c0001t0001g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.984+1287_984+1288i others(226): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(215): Show |
3 | a0002c0004t0003g0133 a0002c0004t0003g0142 a0002c0004t0003g0143 |
3 | HG02257.hp2 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.984+1287_984+1288i others(224): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310557 | G | GGCCCGGA others(238): Show |
7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+1287_984+1288i others(247): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310557 | |||||||
| chr19:310582 | G | C | 1 | a0001c0010t0001g0017 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1263C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310582 | |||||||
| chr19:310590 | C | CAGAAACA others(196): Show |
1 | a0001c0010t0001g0017 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1254_984+1255i others(205): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310590 | |||||||
| chr19:310599 | A | G | 1 | a0001c0010t0001g0017 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1246T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310599 | |||||||
| chr19:310603 | G | A | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.984+1242C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310603 | |||||||
| chr19:310610 | A | G | 1 | a0001c0010t0001g0017 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1235T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310610 | |||||||
| chr19:310611 | T | C | 1 | a0001c0010t0001g0017 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1234A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310611 | |||||||
| chr19:310621 | G | GC | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+1223dupG | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310621 | |||||||
| chr19:310624 | C | G | 1 | a0001c0010t0001g0017 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.984+1221G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310624 | |||||||
| chr19:310636 | A | AACACAGC others(409): Show |
1 | a0001c0002t0002g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.984+1208_984+1209i others(418): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310636 | A | AACACAGC others(430): Show |
6 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.984+1208_984+1209i others(439): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310636 | A | AACGGCCC others(345): Show |
2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310636 | A | AACGGCCC others(366): Show |
5 | a0001c0005t0002g0013 a0001c0005t0002g0129 a0001c0005t0002g0130 others(2): Show |
6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.984+1208_984+1209i others(375): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310636 | A | AACGGCCC others(345): Show |
2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310636 | A | AACGGCCC others(366): Show |
1 | a0001c0002t0002g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.984+1208_984+1209i others(375): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310636 | A | AACGGCCC others(345): Show |
23 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(20): Show |
24 | HG01099.hp1 HG01109.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310636 | A | AACGGCCC others(345): Show |
1 | a0001c0003t0002g0163 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310636 | A | AACGGCCC others(345): Show |
16 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(13): Show |
17 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.984+1208_984+1209i others(354): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310636 | |||||||
| chr19:310639 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.984+1206T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310639 | |||||||
| chr19:310700 | C | T | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+1145G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310700 | |||||||
| chr19:310726 | C | T | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+1119G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310726 | |||||||
| chr19:310780 | C | T | 2 | a0001c0002t0002g0114 a0001c0002t0002g0115 |
2 | HG02300.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.984+1065G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310780 | |||||||
| chr19:310842 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0280 |
2 | HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.984+1003C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310842 | |||||||
| chr19:310862 | C | T | 1 | a0001c0003t0002g0153 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.984+983G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310862 | |||||||
| chr19:310883 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.984+962A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310883 | |||||||
| chr19:310934 | G | A | 2 | a0001c0001t0001g0016 a0001c0007t0001g0174 |
3 | HG01884.hp1 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.984+911C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310934 | |||||||
| chr19:310938 | C | G | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+907G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310938 | |||||||
| chr19:310993 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.984+852G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 310993 | |||||||
| chr19:311037 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(202): Show |
231 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.984+808T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311037 | |||||||
| chr19:311097 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.984+748C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311097 | |||||||
| chr19:311100 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.984+745G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311100 | |||||||
| chr19:311128 | G | A | 2 | a0001c0011t0002g0267 a0001c0011t0002g0283 |
2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.984+717C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311128 | |||||||
| chr19:311138 | C | A | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.984+707G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311138 | |||||||
| chr19:311282 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.984+563C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311282 | |||||||
| chr19:311423 | G | A | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.984+422C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311423 | |||||||
| chr19:311577 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.984+268A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311577 | |||||||
| chr19:311632 | A | G | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.984+213T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311632 | |||||||
| chr19:311696 | C | T | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.984+149G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311696 | |||||||
| chr19:311708 | A | G | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.984+137T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311708 | |||||||
| chr19:311729 | G | A | 2 | a0001c0001t0001g0179 a0001c0002t0002g0121 |
2 | HG01243.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.984+116C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311729 | |||||||
| chr19:311787 | C | G | 29 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(26): Show |
31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.984+58G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311787 | |||||||
| chr19:311825 | C | G | 22 | a0001c0001t0001g0030 a0001c0001t0001g0055 a0001c0001t0001g0306 others(19): Show |
23 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.984+20G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 10/13 | chr19 | 311825 | |||||||
| chr19:311962 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.890-23G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311962 | |||||||
| chr19:311972 | T | TGCCCAGG others(164): Show |
1 | a0001c0001t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.890-34_890-33insGC others(169): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311972 | |||||||
| chr19:311972 | TGCCCAGG others(50): Show |
T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(132): Show |
158 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.890-90_890-34delGC others(55): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311972 | |||||||
| chr19:311972 | TGCCCAGG others(107): Show |
T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0052 |
2 | HG02698.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.889+105_890-34del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311972 | |||||||
| chr19:311982 | GGGGCCGC others(49): Show |
G | 1 | a0001c0001t0001g0230 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.890-99_890-44delGC others(54): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311982 | |||||||
| chr19:311991 | G | A | 1 | a0001c0002t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.890-52C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311991 | |||||||
| chr19:311993 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.890-54C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 311993 | |||||||
| chr19:312020 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0165 |
2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.890-81T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312020 | |||||||
| chr19:312020 | AGTCAGCG others(50): Show |
A | 2 | a0001c0001t0001g0074 a0001c0001t0012g0071 |
2 | HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.889+114_890-82delC others(56): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312020 | |||||||
| chr19:312026 | C | T | 29 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(26): Show |
31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.890-87G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312026 | |||||||
| chr19:312027 | G | GGCGCCCA others(50): Show |
1 | a0001c0001t0001g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.890-89_890-88insTG others(55): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312027 | |||||||
| chr19:312046 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.890-107G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312046 | |||||||
| chr19:312067 | C | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0315 a0001c0001t0001g0319 others(6): Show |
10 | HG03669.hp1 NA18943.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.889+124G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312067 | |||||||
| chr19:312083 | C | T | 1 | a0001c0002t0002g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.889+108G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312083 | |||||||
| chr19:312084 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0165 |
2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.889+107C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312084 | |||||||
| chr19:312086 | CGCCCAGG others(50): Show |
C | 2 | a0001c0001t0001g0009 a0001c0002t0002g0115 |
3 | HG02300.hp1 NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.889+48_889+104delA others(56): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312086 | |||||||
| chr19:312096 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.889+95C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312096 | |||||||
| chr19:312106 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.889+85G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312106 | |||||||
| chr19:312107 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.889+84C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312107 | |||||||
| chr19:312122 | GCCGGGGA others(50): Show |
G | 9 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.889+12_889+68delTC others(55): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312122 | |||||||
| chr19:312141 | A | G | 45 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(42): Show |
48 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.889+50T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312141 | |||||||
| chr19:312143 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.889+48A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312143 | |||||||
| chr19:312153 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.889+38C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312153 | |||||||
| chr19:312164 | G | A | 23 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(20): Show |
24 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.889+27C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312164 | |||||||
| chr19:312173 | G | C | 1 | a0001c0001t0002g0169 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.889+18C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312173 | |||||||
| chr19:312179 | A | G | 47 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(44): Show |
50 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.889+12T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312179 | |||||||
| chr19:312181 | C | T | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.889+10G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 9/13 | chr19 | 312181 | |||||||
| chr19:312311 | G | C | 70 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(67): Show |
73 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.808-39C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312311 | |||||||
| chr19:312313 | A | G | 29 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(26): Show |
31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.808-41T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312313 | |||||||
| chr19:312395 | A | AGCCACCT others(62): Show |
1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.808-192_808-124dup others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | |||||||
| chr19:312395 | A | AGCCACCT others(131): Show |
3 | a0001c0009t0001g0042 a0001c0009t0001g0062 a0001c0009t0001g0077 |
3 | HG01175.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.808-261_808-124dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | |||||||
| chr19:312395 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.808-123T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | |||||||
| chr19:312395 | AGCCACCT others(62): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.808-192_808-124del others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | |||||||
| chr19:312395 | AGCCACCT others(338): Show |
A | 1 | a0001c0001t0001g0055 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.808-468_808-124del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | |||||||
| chr19:312395 | AGCCACCT others(476): Show |
A | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.808-606_808-124del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312395 | |||||||
| chr19:312489 | G | C | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.808-217C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312489 | |||||||
| chr19:312492 | A | ACATCAGG others(62): Show |
28 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(25): Show |
30 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.808-221_808-220ins others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312492 | |||||||
| chr19:312492 | A | G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.808-220T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312492 | |||||||
| chr19:312492 | ACATCAGG others(131): Show |
A | 5 | a0001c0001t0005g0031 a0001c0001t0005g0305 a0001c0001t0005g0328 others(2): Show |
6 | HG02109.hp1 HG03195.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-358_808-221del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312492 | |||||||
| chr19:312524 | C | T | 4 | a0001c0001t0001g0308 a0001c0001t0001g0311 a0001c0001t0001g0316 others(1): Show |
4 | HG02135.hp1 NA18612.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.808-252G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312524 | |||||||
| chr19:312533 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG01261.hp2 NA18945.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.808-261C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312533 | |||||||
| chr19:312533 | G | GGCCACCT others(131): Show |
1 | a0001c0002t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.808-262_808-261ins others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312533 | |||||||
| chr19:312533 | GGCCACCT others(62): Show |
G | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.808-330_808-262del others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312533 | |||||||
| chr19:312558 | G | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(6): Show |
10 | HG01261.hp2 HG03209.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.808-286C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312558 | |||||||
| chr19:312561 | A | G | 10 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
11 | HG01261.hp2 HG03209.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.808-289T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312561 | |||||||
| chr19:312594 | GATGTCAG others(269): Show |
G | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.808-598_808-323del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312594 | |||||||
| chr19:312602 | A | G | 14 | a0001c0001t0001g0024 a0001c0001t0001g0095 a0001c0001t0001g0190 others(11): Show |
15 | HG01261.hp2 HG02135.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.808-330T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312602 | |||||||
| chr19:312627 | C | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(6): Show |
10 | HG01261.hp2 HG03209.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.808-355G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312627 | |||||||
| chr19:312630 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(6): Show |
10 | HG01261.hp2 HG03209.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.808-358C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312630 | |||||||
| chr19:312630 | G | GCATCAGG others(62): Show |
10 | a0001c0001t0001g0065 a0001c0001t0001g0145 a0001c0001t0001g0167 others(7): Show |
10 | HG00741.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.808-427_808-359dup others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312630 | |||||||
| chr19:312630 | G | GCATCAGG others(131): Show |
2 | a0001c0013t0001g0257 a0001c0013t0001g0258 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.808-496_808-359dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312630 | |||||||
| chr19:312642 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-370C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312642 | |||||||
| chr19:312663 | GATGTCAG others(200): Show |
G | 1 | a0002c0004t0003g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.808-598_808-392del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312663 | |||||||
| chr19:312671 | G | A | 1 | a0001c0005t0002g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.808-399C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312671 | |||||||
| chr19:312696 | G | C | 3 | a0001c0005t0002g0131 a0001c0014t0002g0032 a0001c0014t0002g0033 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.808-424C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312696 | |||||||
| chr19:312699 | A | G | 3 | a0001c0005t0002g0131 a0001c0014t0002g0032 a0001c0014t0002g0033 |
3 | HG02109.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.808-427T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312699 | |||||||
| chr19:312711 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-439C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312711 | |||||||
| chr19:312732 | G | A | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.808-460C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312732 | |||||||
| chr19:312732 | GATGTCAG others(131): Show |
G | 18 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0105 others(15): Show |
19 | HG00140.hp2 HG00642.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.808-598_808-461del | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312732 | |||||||
| chr19:312740 | G | A | 24 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(21): Show |
25 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.808-468C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312740 | |||||||
| chr19:312765 | G | C | 24 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(21): Show |
25 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.808-493C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312765 | |||||||
| chr19:312768 | A | G | 24 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(21): Show |
25 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.808-496T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312768 | |||||||
| chr19:312779 | C | T | 1 | a0001c0002t0002g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.808-507G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312779 | |||||||
| chr19:312780 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.808-508C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312780 | |||||||
| chr19:312809 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-537C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312809 | |||||||
| chr19:312834 | G | C | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-562C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312834 | |||||||
| chr19:312837 | A | G | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.808-565T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312837 | |||||||
| chr19:312870 | A | AATGTCAG others(62): Show |
1 | a0001c0001t0004g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.808-599_808-598ins others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312870 | |||||||
| chr19:312870 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.808-598T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312870 | |||||||
| chr19:312878 | G | A | 6 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(3): Show |
6 | HG02258.hp1 HG02965.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-606C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312878 | |||||||
| chr19:312903 | G | C | 34 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(31): Show |
36 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.807+589C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312903 | |||||||
| chr19:312906 | A | G | 34 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(31): Show |
36 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.807+586T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312906 | |||||||
| chr19:312918 | G | A | 1 | a0003c0012t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.807+574C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312918 | |||||||
| chr19:312972 | G | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0285 a0001c0001t0002g0023 others(28): Show |
35 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.807+520C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312972 | |||||||
| chr19:312975 | A | ACATCAGG others(131): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0310 |
2 | HG01981.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.807+379_807+516dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312975 | |||||||
| chr19:312975 | A | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0285 a0001c0001t0002g0023 others(28): Show |
35 | HG00099.hp2 HG00323.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.807+517T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312975 | |||||||
| chr19:312987 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.807+505C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 312987 | |||||||
| chr19:313008 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.807+484C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313008 | |||||||
| chr19:313013 | C | G | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.807+479G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313013 | |||||||
| chr19:313016 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0285 |
4 | HG00099.hp2 HG00323.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+476C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313016 | |||||||
| chr19:313016 | G | GGCCACCT others(62): Show |
8 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
9 | HG01261.hp2 NA18945.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.807+475_807+476ins others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313016 | |||||||
| chr19:313016 | G | GGCCACCT others(131): Show |
1 | a0001c0001t0001g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.807+338_807+475dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313016 | |||||||
| chr19:313041 | G | C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0260 others(51): Show |
60 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.807+451C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313041 | |||||||
| chr19:313044 | A | ACATCAGG others(131): Show |
35 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0027 others(32): Show |
42 | HG00140.hp1 HG00438.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.807+310_807+447dup others(138): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | |||||||
| chr19:313044 | A | ACATCAGG others(200): Show |
4 | a0001c0001t0001g0266 a0001c0001t0001g0282 a0001c0001t0001g0291 others(1): Show |
4 | HG00741.hp1 HG01074.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.807+447_807+448ins others(207): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | |||||||
| chr19:313044 | A | ACATCAGG others(269): Show |
6 | a0001c0002t0002g0113 a0001c0002t0002g0114 a0001c0002t0002g0115 others(3): Show |
6 | HG01081.hp2 HG01978.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+447_807+448ins others(276): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | |||||||
| chr19:313044 | A | G | 54 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0260 others(51): Show |
60 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.807+448T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | |||||||
| chr19:313044 | ACATCAGG others(62): Show |
A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0236 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.807+379_807+447del others(69): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313044 | |||||||
| chr19:313055 | C | T | 2 | a0001c0011t0002g0267 a0001c0011t0002g0283 |
2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.807+437G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313055 | |||||||
| chr19:313077 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0191 a0001c0001t0001g0213 others(2): Show |
6 | HG00438.hp2 HG00597.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.807+415C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313077 | |||||||
| chr19:313085 | G | A | 19 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(16): Show |
20 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.807+407C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313085 | |||||||
| chr19:313110 | C | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(96): Show |
119 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.807+382G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313110 | |||||||
| chr19:313113 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(96): Show |
119 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.807+379C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313113 | |||||||
| chr19:313125 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.807+367C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313125 | |||||||
| chr19:313153 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.807+339C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313153 | |||||||
| chr19:313154 | A | G | 74 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0066 others(71): Show |
79 | HG00673.hp1 HG00735.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.807+338T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313154 | |||||||
| chr19:313179 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.807+313G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313179 | |||||||
| chr19:313182 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.807+310C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313182 | |||||||
| chr19:313204 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.807+288A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313204 | |||||||
| chr19:313302 | T | A | 51 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0001g0238 others(48): Show |
54 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.807+190A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313302 | |||||||
| chr19:313318 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.807+174C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313318 | |||||||
| chr19:313450 | G | A | 1 | a0004c0019t0001g0203 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.807+42C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 8/13 | chr19 | 313450 | |||||||
| chr19:313704 | G | A | 7 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(4): Show |
7 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-61C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313704 | |||||||
| chr19:313779 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.656-136G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313779 | |||||||
| chr19:313790 | T | C | 57 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(54): Show |
60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.656-147A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313790 | |||||||
| chr19:313890 | G | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18991.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.656-247C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313890 | |||||||
| chr19:313897 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.656-254C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 313897 | |||||||
| chr19:314107 | C | T | 6 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-464G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314107 | |||||||
| chr19:314108 | G | A | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-465C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314108 | |||||||
| chr19:314115 | C | G | 57 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(54): Show |
60 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.656-472G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314115 | |||||||
| chr19:314130 | G | T | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.656-487C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314130 | |||||||
| chr19:314161 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.656-518T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314161 | |||||||
| chr19:314176 | C | G | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-533G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314176 | |||||||
| chr19:314182 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656-539G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314182 | |||||||
| chr19:314362 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.656-719C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314362 | |||||||
| chr19:314542 | C | T | 8 | a0002c0004t0003g0106 a0002c0004t0003g0134 a0002c0004t0003g0135 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-899G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314542 | |||||||
| chr19:314570 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.656-927G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314570 | |||||||
| chr19:314755 | C | T | 29 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(26): Show |
31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.656-1112G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314755 | |||||||
| chr19:314793 | C | T | 1 | a0001c0003t0002g0163 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.656-1150G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314793 | |||||||
| chr19:314832 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.656-1189C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314832 | |||||||
| chr19:314933 | G | A | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-1290C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314933 | |||||||
| chr19:314977 | G | T | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-1334C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314977 | |||||||
| chr19:314994 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0093 others(2): Show |
6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-1351A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 314994 | |||||||
| chr19:315024 | C | T | 6 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0208 others(3): Show |
6 | HG00741.hp2 HG01261.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-1381G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315024 | |||||||
| chr19:315136 | G | A | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-1493C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315136 | |||||||
| chr19:315172 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.656-1529G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315172 | |||||||
| chr19:315179 | AC | A | 50 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-1537delG | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315179 | |||||||
| chr19:315221 | C | G | 1 | a0007c0020t0010g0050 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.656-1578G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315221 | |||||||
| chr19:315222 | G | C | 1 | a0007c0020t0010g0050 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.656-1579C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315222 | |||||||
| chr19:315224 | G | A | 29 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0002t0002g0109 others(26): Show |
31 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.656-1581C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315224 | |||||||
| chr19:315320 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.656-1677C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315320 | |||||||
| chr19:315322 | G | A | 58 | a0001c0001t0002g0023 a0001c0001t0002g0169 a0001c0001t0004g0061 others(55): Show |
61 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.656-1679C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315322 | |||||||
| chr19:315344 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.656-1701C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315344 | |||||||
| chr19:315361 | G | A | 1 | a0001c0001t0001g0314 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.656-1718C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315361 | |||||||
| chr19:315552 | C | T | 49 | a0001c0001t0002g0023 a0001c0002t0002g0109 a0001c0002t0002g0110 others(46): Show |
52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.656-1909G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315552 | |||||||
| chr19:315759 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.656-2116T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315759 | |||||||
| chr19:315788 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
254 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.656-2145C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315788 | |||||||
| chr19:315816 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.656-2173G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315816 | |||||||
| chr19:315919 | A | G | 49 | a0001c0001t0002g0023 a0001c0002t0002g0109 a0001c0002t0002g0110 others(46): Show |
52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.656-2276T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315919 | |||||||
| chr19:315954 | G | A | 49 | a0001c0001t0002g0023 a0001c0002t0002g0109 a0001c0002t0002g0110 others(46): Show |
52 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.656-2311C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 315954 | |||||||
| chr19:316040 | T | C | 50 | a0001c0001t0002g0023 a0001c0001t0007g0092 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-2397A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316040 | |||||||
| chr19:316154 | A | C | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-2511T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316154 | |||||||
| chr19:316245 | CA | C | 8 | a0002c0004t0003g0106 a0002c0004t0003g0134 a0002c0004t0003g0135 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.656-2603delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316245 | |||||||
| chr19:316297 | A | AAT | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-2655_656-2654i others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316297 | |||||||
| chr19:316297 | A | ATT | 27 | a0001c0001t0002g0023 a0001c0002t0001g0238 a0001c0002t0002g0109 others(24): Show |
28 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.656-2656_656-2655d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316297 | |||||||
| chr19:316352 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.656-2709C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316352 | |||||||
| chr19:316385 | G | A | 55 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0126 others(52): Show |
59 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.656-2742C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316385 | |||||||
| chr19:316437 | T | C | 2 | a0001c0006t0001g0014 a0001c0006t0001g0137 |
3 | HG02451.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.656-2794A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316437 | |||||||
| chr19:316438 | G | GTCC | 2 | a0001c0006t0001g0014 a0001c0006t0001g0137 |
3 | HG02451.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.656-2796_656-2795i others(5): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316438 | |||||||
| chr19:316439 | C | A | 2 | a0001c0006t0001g0014 a0001c0006t0001g0137 |
3 | HG02451.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.656-2796G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316439 | |||||||
| chr19:316542 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.656-2899C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316542 | |||||||
| chr19:316689 | C | G | 1 | a0001c0013t0001g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.656-3046G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316689 | |||||||
| chr19:316721 | A | G | 6 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-3078T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316721 | |||||||
| chr19:316792 | C | A | 50 | a0001c0001t0002g0023 a0001c0002t0001g0238 a0001c0002t0002g0109 others(47): Show |
53 | HG00735.hp2 HG01071.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.656-3149G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316792 | |||||||
| chr19:316907 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.656-3264A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 316907 | |||||||
| chr19:317098 | A | T | 1 | a0001c0001t0004g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656-3455T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317098 | |||||||
| chr19:317118 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656-3475C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317118 | |||||||
| chr19:317161 | G | A | 17 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(14): Show |
18 | HG00735.hp2 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.656-3518C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317161 | |||||||
| chr19:317165 | T | TGGGCGGA others(126): Show |
1 | a0001c0003t0002g0158 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.656-3523_656-3522i others(135): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317165 | |||||||
| chr19:317203 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(211): Show |
242 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.656-3560C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317203 | |||||||
| chr19:317204 | C | A | 1 | a0001c0001t0004g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656-3561G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317204 | |||||||
| chr19:317249 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0188 |
2 | HG00738.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.656-3606G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317249 | |||||||
| chr19:317293 | T | C | 38 | a0001c0001t0001g0264 a0001c0001t0001g0272 a0001c0001t0001g0279 others(35): Show |
40 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.656-3650A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317293 | |||||||
| chr19:317294 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(38): Show |
51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.656-3651C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317294 | |||||||
| chr19:317298 | C | T | 2 | a0001c0011t0002g0267 a0001c0011t0002g0283 |
2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.656-3655G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317298 | |||||||
| chr19:317313 | G | T | 1 | a0001c0005t0002g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.656-3670C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317313 | |||||||
| chr19:317331 | C | T | 4 | a0001c0001t0001g0287 a0001c0001t0001g0303 a0001c0005t0002g0244 others(1): Show |
4 | HG01346.hp1 HG02895.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-3688G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317331 | |||||||
| chr19:317334 | G | C | 1 | a0001c0005t0002g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.656-3691C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317334 | |||||||
| chr19:317334 | G | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0303 a0001c0027t0001g0160 |
3 | HG01346.hp1 NA18999.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.656-3691C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317334 | |||||||
| chr19:317343 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.656-3700G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317343 | |||||||
| chr19:317353 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.656-3710A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317353 | |||||||
| chr19:317354 | C | T | 25 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0126 others(22): Show |
27 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-3711G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317354 | |||||||
| chr19:317355 | G | A | 1 | a0001c0001t0011g0265 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.656-3712C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317355 | |||||||
| chr19:317387 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(242): Show |
281 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.656-3744T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317387 | |||||||
| chr19:317399 | T | C | 39 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0055 others(36): Show |
42 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-3756A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317399 | |||||||
| chr19:317430 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(45): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-3787T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317430 | |||||||
| chr19:317432 | CAGG | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(45): Show |
57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-3792_656-3790d others(5): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317432 | |||||||
| chr19:317440 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.656-3797A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317440 | |||||||
| chr19:317475 | T | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0012g0071 |
3 | HG02698.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.656-3832A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317475 | |||||||
| chr19:317498 | A | G | 32 | a0001c0001t0002g0023 a0001c0002t0001g0238 a0001c0002t0002g0109 others(29): Show |
34 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.656-3855T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317498 | |||||||
| chr19:317519 | T | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(200): Show |
230 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.656-3876A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317519 | |||||||
| chr19:317519 | T | G | 1 | a0001c0001t0004g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-3876A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317519 | |||||||
| chr19:317531 | A | AAAAT | 8 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0067 others(5): Show |
9 | HG02055.hp2 HG02523.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-3892_656-3889d others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | |||||||
| chr19:317531 | A | AAAATAAA others(1): Show |
54 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0104 others(51): Show |
57 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.656-3896_656-3889d others(10): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | |||||||
| chr19:317531 | A | AAAATAAA others(5): Show |
76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(73): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.656-3900_656-3889d others(14): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | |||||||
| chr19:317531 | A | AAAATAAA others(9): Show |
9 | a0001c0001t0001g0020 a0001c0001t0001g0167 a0001c0001t0001g0176 others(6): Show |
10 | HG01255.hp1 HG02257.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.656-3904_656-3889d others(18): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | |||||||
| chr19:317531 | AAAATAAA others(5): Show |
A | 6 | a0001c0001t0001g0281 a0001c0001t0001g0286 a0001c0005t0002g0244 others(3): Show |
6 | HG00140.hp1 HG01255.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-3900_656-3889d others(14): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317531 | |||||||
| chr19:317563 | T | TAAATAAA others(5): Show |
3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0169 |
3 | HG01099.hp1 HG01167.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.656-3921_656-3920i others(14): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317563 | |||||||
| chr19:317564 | A | AAATAAAT others(4): Show |
1 | a0001c0001t0004g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.656-3922_656-3921i others(13): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317564 | |||||||
| chr19:317702 | C | G | 25 | a0001c0001t0002g0023 a0001c0002t0002g0109 a0001c0002t0002g0110 others(22): Show |
26 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-4059G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317702 | |||||||
| chr19:317730 | C | CA | 7 | a0001c0001t0001g0067 a0001c0001t0001g0207 a0001c0001t0001g0259 others(4): Show |
7 | HG01358.hp1 HG02602.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-4088dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317730 | |||||||
| chr19:317730 | CA | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(99): Show |
122 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.656-4088delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317730 | |||||||
| chr19:317740 | A | C | 4 | a0001c0005t0002g0244 a0001c0005t0002g0245 a0001c0014t0002g0032 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-4097T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317740 | |||||||
| chr19:317744 | A | C | 5 | a0001c0002t0001g0238 a0001c0005t0002g0244 a0001c0005t0002g0245 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-4101T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317744 | |||||||
| chr19:317926 | G | A | 2 | a0001c0001t0001g0318 a0001c0002t0002g0109 |
2 | HG02922.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.656-4283C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317926 | |||||||
| chr19:317970 | G | A | 2 | a0001c0002t0002g0119 a0002c0015t0003g0242 |
2 | HG01978.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.656-4327C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 317970 | |||||||
| chr19:318238 | T | C | 33 | a0001c0001t0002g0023 a0001c0002t0001g0238 a0001c0002t0002g0109 others(30): Show |
35 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.656-4595A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318238 | |||||||
| chr19:318308 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
299 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.656-4665A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318308 | |||||||
| chr19:318423 | G | A | 39 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0030 others(36): Show |
42 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-4780C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318423 | |||||||
| chr19:318466 | A | T | 1 | a0001c0001t0001g0322 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656-4823T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318466 | |||||||
| chr19:318471 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656-4828C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318471 | |||||||
| chr19:318586 | G | A | 67 | a0001c0001t0002g0023 a0001c0002t0001g0238 a0001c0002t0002g0109 others(64): Show |
71 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.656-4943C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318586 | |||||||
| chr19:318624 | A | G | 51 | a0001c0001t0002g0023 a0001c0002t0001g0238 a0001c0002t0002g0109 others(48): Show |
54 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-4981T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318624 | |||||||
| chr19:318778 | T | C | 51 | a0001c0001t0002g0023 a0001c0002t0001g0238 a0001c0002t0002g0109 others(48): Show |
54 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.656-5135A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318778 | |||||||
| chr19:318783 | G | A | 1 | a0001c0002t0002g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.656-5140C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318783 | |||||||
| chr19:318913 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.656-5270G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318913 | |||||||
| chr19:318914 | G | A | 13 | a0001c0006t0001g0014 a0001c0006t0001g0137 a0001c0006t0003g0141 others(10): Show |
14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-5271C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318914 | |||||||
| chr19:318929 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.656-5286G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 318929 | |||||||
| chr19:319050 | T | A | 1 | a0001c0001t0001g0322 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656-5407A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319050 | |||||||
| chr19:319055 | C | CA | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.656-5413dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319055 | |||||||
| chr19:319055 | C | CAA | 29 | a0001c0001t0001g0086 a0001c0001t0001g0164 a0001c0001t0001g0217 others(26): Show |
30 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.656-5414_656-5413d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319055 | |||||||
| chr19:319055 | C | CAAAA | 19 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(16): Show |
19 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.656-5416_656-5413d others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319055 | |||||||
| chr19:319055 | C | CAAAAA | 7 | a0001c0002t0002g0122 a0001c0005t0002g0013 a0001c0005t0002g0129 others(4): Show |
8 | HG01192.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-5417_656-5413d others(7): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319055 | |||||||
| chr19:319230 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG00673.hp1 HG01952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.656-5587G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319230 | |||||||
| chr19:319349 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-5706C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319349 | |||||||
| chr19:319371 | C | A | 49 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(46): Show |
51 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.656-5728G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319371 | |||||||
| chr19:319373 | A | C | 13 | a0001c0006t0001g0014 a0001c0006t0001g0137 a0001c0006t0003g0141 others(10): Show |
14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-5730T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319373 | |||||||
| chr19:319444 | A | G | 30 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(27): Show |
31 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.656-5801T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319444 | |||||||
| chr19:319466 | T | G | 5 | a0001c0005t0002g0013 a0001c0005t0002g0129 a0001c0005t0002g0130 others(2): Show |
6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-5823A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319466 | |||||||
| chr19:319605 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(54): Show |
67 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.656-5962G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319605 | |||||||
| chr19:319720 | G | C | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+5915C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319720 | |||||||
| chr19:319760 | C | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+5875G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319760 | |||||||
| chr19:319806 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.655+5829A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319806 | |||||||
| chr19:319822 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(137): Show |
164 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.655+5813C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319822 | |||||||
| chr19:319994 | C | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0093 others(2): Show |
6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+5641G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 319994 | |||||||
| chr19:320023 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
299 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.655+5612G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320023 | |||||||
| chr19:320081 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.655+5554G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320081 | |||||||
| chr19:320097 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(72): Show |
92 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.655+5538C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320097 | |||||||
| chr19:320143 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+5492C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320143 | |||||||
| chr19:320145 | C | T | 6 | a0001c0002t0002g0113 a0001c0002t0002g0114 a0001c0002t0002g0115 others(3): Show |
6 | HG01081.hp2 HG01978.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+5490G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320145 | |||||||
| chr19:320220 | C | CA | 58 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(55): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.655+5414dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320220 | |||||||
| chr19:320237 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.655+5398C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320237 | |||||||
| chr19:320250 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0066 others(1): Show |
7 | HG00280.hp1 HG00738.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+5385C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320250 | |||||||
| chr19:320385 | C | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0289 |
2 | NA18950.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.655+5250G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320385 | |||||||
| chr19:320388 | A | AATAG | 3 | a0001c0009t0001g0042 a0001c0009t0001g0062 a0001c0009t0001g0077 |
3 | HG01175.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.655+5243_655+5246d others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320388 | |||||||
| chr19:320400 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.655+5235C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320400 | |||||||
| chr19:320430 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0220 a0001c0001t0001g0229 others(1): Show |
4 | NA18948.hp2 NA18952.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+5205A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320430 | |||||||
| chr19:320532 | G | A | 1 | a0001c0001t0011g0265 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.655+5103C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320532 | |||||||
| chr19:320557 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.655+5078C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320557 | |||||||
| chr19:320612 | T | C | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+5023A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320612 | |||||||
| chr19:320714 | T | G | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+4921A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320714 | |||||||
| chr19:320794 | G | A | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4841C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320794 | |||||||
| chr19:320892 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.655+4743C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320892 | |||||||
| chr19:320982 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(95): Show |
117 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.655+4653C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 320982 | |||||||
| chr19:321010 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.655+4625A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321010 | |||||||
| chr19:321047 | C | T | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+4588G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321047 | |||||||
| chr19:321048 | G | A | 30 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(27): Show |
31 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+4587C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321048 | |||||||
| chr19:321129 | G | A | 6 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0241 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+4506C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321129 | |||||||
| chr19:321162 | G | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4473C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321162 | |||||||
| chr19:321312 | A | G | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4323T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321312 | |||||||
| chr19:321341 | A | G | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4294T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321341 | |||||||
| chr19:321366 | C | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4269G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321366 | |||||||
| chr19:321434 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(189): Show |
218 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.655+4201A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321434 | |||||||
| chr19:321452 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.655+4183A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321452 | |||||||
| chr19:321460 | C | A | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.655+4175G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321460 | |||||||
| chr19:321566 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
299 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.655+4069A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321566 | |||||||
| chr19:321575 | C | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4060G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321575 | |||||||
| chr19:321584 | T | C | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+4051A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321584 | |||||||
| chr19:321588 | G | A | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.655+4047C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321588 | |||||||
| chr19:321609 | A | G | 7 | a0001c0001t0001g0262 a0001c0001t0001g0266 a0001c0001t0001g0282 others(4): Show |
7 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.655+4026T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321609 | |||||||
| chr19:321627 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655+4008C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321627 | |||||||
| chr19:321682 | A | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+3953T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321682 | |||||||
| chr19:321688 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.655+3947A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321688 | |||||||
| chr19:321706 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0076 |
4 | NA18946.hp2 NA18967.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+3929T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321706 | |||||||
| chr19:321715 | C | T | 1 | a0005c0025t0001g0184 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.655+3920G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321715 | |||||||
| chr19:321874 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(188): Show |
217 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.655+3761A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321874 | |||||||
| chr19:321974 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.655+3661C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321974 | |||||||
| chr19:321983 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.655+3652G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 321983 | |||||||
| chr19:322007 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.655+3628G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322007 | |||||||
| chr19:322036 | C | G | 19 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(16): Show |
20 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.655+3599G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322036 | |||||||
| chr19:322054 | G | A | 27 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0105 others(24): Show |
29 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.655+3581C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322054 | |||||||
| chr19:322093 | C | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+3542G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322093 | |||||||
| chr19:322105 | G | A | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.655+3530C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322105 | |||||||
| chr19:322156 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.655+3479G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322156 | |||||||
| chr19:322436 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0053 |
2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.655+3199C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322436 | |||||||
| chr19:322451 | G | A | 6 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+3184C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322451 | |||||||
| chr19:322460 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.655+3175G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322460 | |||||||
| chr19:322518 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.655+3117G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322518 | |||||||
| chr19:322523 | T | C | 2 | a0001c0002t0002g0121 a0001c0002t0002g0122 |
2 | HG01192.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.655+3112A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322523 | |||||||
| chr19:322645 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0093 others(8): Show |
12 | HG02258.hp1 HG02630.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+2990C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322645 | |||||||
| chr19:322654 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.655+2981A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322654 | |||||||
| chr19:322738 | C | T | 4 | a0001c0002t0002g0117 a0001c0002t0002g0118 a0001c0002t0002g0120 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+2897G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322738 | |||||||
| chr19:322938 | C | T | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+2697G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 322938 | |||||||
| chr19:323013 | C | T | 31 | a0001c0002t0001g0238 a0001c0002t0002g0239 a0001c0002t0002g0240 others(28): Show |
33 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+2622G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323013 | |||||||
| chr19:323076 | A | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0234 |
3 | HG01928.hp1 HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.655+2559T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323076 | |||||||
| chr19:323096 | C | T | 11 | a0001c0002t0002g0239 a0001c0002t0002g0240 a0001c0002t0002g0241 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.655+2539G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323096 | |||||||
| chr19:323098 | C | A | 31 | a0001c0002t0001g0238 a0001c0002t0002g0239 a0001c0002t0002g0240 others(28): Show |
33 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+2537G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323098 | |||||||
| chr19:323180 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.655+2455C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323180 | |||||||
| chr19:323199 | CAAGACAC others(162): Show |
C | 19 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(16): Show |
19 | HG01081.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.655+2267_655+2435d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323199 | |||||||
| chr19:323254 | A | G | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.655+2381T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323254 | |||||||
| chr19:323301 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(238): Show |
278 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.655+2334G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323301 | |||||||
| chr19:323343 | G | C | 31 | a0001c0002t0001g0238 a0001c0002t0002g0239 a0001c0002t0002g0240 others(28): Show |
33 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.655+2292C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323343 | |||||||
| chr19:323442 | C | T | 2 | a0003c0012t0001g0048 a0003c0012t0001g0060 |
2 | HG03654.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.655+2193G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323442 | |||||||
| chr19:323455 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0093 others(2): Show |
6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+2180C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323455 | |||||||
| chr19:323473 | A | G | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+2162T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323473 | |||||||
| chr19:323507 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(138): Show |
165 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.655+2128G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323507 | |||||||
| chr19:323530 | G | A | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+2105C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323530 | |||||||
| chr19:323618 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.655+2017A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323618 | |||||||
| chr19:323710 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.655+1925C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323710 | |||||||
| chr19:323757 | TACACAGG others(415): Show |
T | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1456_655+1877d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323757 | |||||||
| chr19:323764 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.655+1871C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323764 | |||||||
| chr19:323820 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.655+1815G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323820 | |||||||
| chr19:323904 | C | T | 1 | a0001c0002t0002g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+1731G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323904 | |||||||
| chr19:323910 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.655+1725C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323910 | |||||||
| chr19:323918 | T | A | 1 | a0001c0001t0001g0287 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.655+1717A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 323918 | |||||||
| chr19:324024 | G | A | 48 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(45): Show |
50 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.655+1611C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324024 | |||||||
| chr19:324028 | C | T | 1 | a0001c0001t0001g0314 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655+1607G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324028 | |||||||
| chr19:324029 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.655+1606C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324029 | |||||||
| chr19:324058 | ACAC | A | 48 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(45): Show |
50 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.655+1574_655+1576d others(5): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324058 | |||||||
| chr19:324064 | GACACACA others(533): Show |
G | 48 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(45): Show |
50 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.655+1031_655+1570d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324064 | |||||||
| chr19:324143 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.655+1492G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324143 | |||||||
| chr19:324156 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.655+1479G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324156 | |||||||
| chr19:324181 | C | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1454G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324181 | |||||||
| chr19:324183 | C | G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1452G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324183 | |||||||
| chr19:324239 | A | G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1396T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324239 | |||||||
| chr19:324257 | A | G | 3 | a0002c0004t0003g0133 a0002c0004t0003g0142 a0002c0004t0003g0143 |
3 | HG02257.hp2 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.655+1378T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324257 | |||||||
| chr19:324274 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655+1361G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324274 | |||||||
| chr19:324277 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1358C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324277 | |||||||
| chr19:324278 | T | C | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1357A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324278 | |||||||
| chr19:324309 | C | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1326G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324309 | |||||||
| chr19:324316 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1319C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324316 | |||||||
| chr19:324338 | A | G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1297T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324338 | |||||||
| chr19:324345 | C | A | 1 | a0001c0001t0001g0019 | 2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.655+1290G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324345 | |||||||
| chr19:324359 | C | T | 1 | a0001c0001t0001g0019 | 2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.655+1276G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324359 | |||||||
| chr19:324361 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1274C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324361 | |||||||
| chr19:324391 | T | G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1244A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324391 | |||||||
| chr19:324396 | C | T | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1239G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324396 | |||||||
| chr19:324435 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1200C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324435 | |||||||
| chr19:324441 | G | A | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.655+1194C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324441 | |||||||
| chr19:324467 | A | C | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1168T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324467 | |||||||
| chr19:324474 | T | C | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1161A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324474 | |||||||
| chr19:324480 | A | G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1155T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324480 | |||||||
| chr19:324501 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): Show |
235 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.655+1134A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324501 | |||||||
| chr19:324502 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1133C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324502 | |||||||
| chr19:324518 | A | G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1117T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324518 | |||||||
| chr19:324539 | GACACACA others(58): Show |
G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+1031_655+1095d others(67): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324539 | |||||||
| chr19:324663 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.655+972G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324663 | |||||||
| chr19:324665 | C | A | 1 | a0008c0016t0001g0195 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.655+970G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324665 | |||||||
| chr19:324675 | C | T | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+960G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324675 | |||||||
| chr19:324687 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.655+948C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324687 | |||||||
| chr19:324707 | C | T | 30 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(27): Show |
31 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+928G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324707 | |||||||
| chr19:324738 | G | A | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.655+897C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324738 | |||||||
| chr19:324824 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(128): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.655+811T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324824 | |||||||
| chr19:324920 | T | C | 13 | a0001c0006t0001g0014 a0001c0006t0001g0137 a0001c0006t0003g0141 others(10): Show |
14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.655+715A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 324920 | |||||||
| chr19:325093 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(189): Show |
218 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.655+542T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325093 | |||||||
| chr19:325171 | G | A | 1 | a0001c0002t0002g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+464C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325171 | |||||||
| chr19:325198 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.655+437C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325198 | |||||||
| chr19:325266 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(190): Show |
219 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.655+369A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325266 | |||||||
| chr19:325268 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.655+367G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325268 | |||||||
| chr19:325281 | G | C | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.655+354C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325281 | |||||||
| chr19:325309 | T | G | 1 | a0001c0001t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.655+326A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325309 | |||||||
| chr19:325310 | C | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.655+325G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325310 | |||||||
| chr19:325319 | C | T | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+316G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325319 | |||||||
| chr19:325320 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.655+315C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325320 | |||||||
| chr19:325424 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.655+211G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325424 | |||||||
| chr19:325452 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01952.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.655+183C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325452 | |||||||
| chr19:325481 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(99): Show |
122 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.655+154G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325481 | |||||||
| chr19:325513 | C | T | 2 | a0001c0013t0001g0257 a0001c0013t0001g0258 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.655+122G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325513 | |||||||
| chr19:325514 | A | G | 51 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0002g0023 others(48): Show |
54 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.655+121T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325514 | |||||||
| chr19:325539 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.655+96G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325539 | |||||||
| chr19:325584 | C | A | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG00673.hp1 HG01952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.655+51G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 7/13 | chr19 | 325584 | |||||||
| chr19:325747 | T | C | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.586-43A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 325747 | |||||||
| chr19:325801 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.586-97G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 325801 | |||||||
| chr19:325865 | A | G | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.586-161T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 325865 | |||||||
| chr19:325969 | G | A | 4 | a0001c0002t0002g0117 a0001c0002t0002g0118 a0001c0002t0002g0120 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-265C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 325969 | |||||||
| chr19:326059 | G | C | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.586-355C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326059 | |||||||
| chr19:326089 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.586-385G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326089 | |||||||
| chr19:326146 | A | C | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+361T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326146 | |||||||
| chr19:326179 | G | A | 13 | a0001c0006t0001g0014 a0001c0006t0001g0137 a0001c0006t0003g0141 others(10): Show |
14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.585+328C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326179 | |||||||
| chr19:326198 | A | G | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+309T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326198 | |||||||
| chr19:326215 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.585+292C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326215 | |||||||
| chr19:326250 | C | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0093 others(8): Show |
12 | HG02258.hp1 HG02630.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.585+257G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326250 | |||||||
| chr19:326254 | T | C | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+253A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326254 | |||||||
| chr19:326311 | C | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+196G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326311 | |||||||
| chr19:326326 | C | CGGGATGC others(65): Show |
50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+180_585+181ins others(72): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326326 | |||||||
| chr19:326384 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.585+123C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326384 | |||||||
| chr19:326390 | G | A | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.585+117C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326390 | |||||||
| chr19:326392 | C | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.585+115G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326392 | |||||||
| chr19:326435 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.585+72C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326435 | |||||||
| chr19:326467 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.585+40C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326467 | |||||||
| chr19:326481 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(94): Show |
116 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.585+26C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 6/13 | chr19 | 326481 | |||||||
| chr19:326652 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.494-54G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326652 | |||||||
| chr19:326723 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0011g0265 |
2 | HG02523.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.494-125A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326723 | |||||||
| chr19:326818 | G | C | 15 | a0001c0001t0001g0150 a0001c0001t0001g0164 a0001c0001t0001g0165 others(12): Show |
16 | HG00642.hp1 HG01099.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.494-220C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326818 | |||||||
| chr19:326936 | G | A | 6 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+197C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326936 | |||||||
| chr19:326964 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+169G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 326964 | |||||||
| chr19:327078 | C | A | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.493+55G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 5/13 | chr19 | 327078 | |||||||
| chr19:327260 | T | TA | 50 | a0001c0001t0001g0250 a0001c0001t0001g0318 a0001c0002t0001g0238 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
splice_region_variant&intron_variant | LOW | c.370-5dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327260 | |||||||
| chr19:327260 | TA | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0047 others(13): Show |
16 | HG00738.hp1 HG01099.hp1 HG01167.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.370-5delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327260 | |||||||
| chr19:327271 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.370-15T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327271 | |||||||
| chr19:327283 | A | C | 2 | a0001c0003t0002g0155 a0001c0003t0002g0161 |
2 | HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.370-27T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327283 | |||||||
| chr19:327323 | T | C | 51 | a0001c0001t0001g0237 a0001c0002t0001g0238 a0001c0002t0002g0109 others(48): Show |
53 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.370-67A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327323 | |||||||
| chr19:327411 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.370-155C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327411 | |||||||
| chr19:327436 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.370-180C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327436 | |||||||
| chr19:327597 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.369+267G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327597 | |||||||
| chr19:327683 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(137): Show |
164 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.369+181C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327683 | |||||||
| chr19:327706 | A | G | 6 | a0001c0001t0004g0061 a0001c0001t0004g0073 a0001c0001t0004g0253 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+158T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327706 | |||||||
| chr19:327821 | C | A | 32 | a0001c0001t0002g0023 a0001c0002t0001g0238 a0001c0002t0002g0109 others(29): Show |
34 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.369+43G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327821 | |||||||
| chr19:327840 | G | C | 1 | a0001c0001t0001g0276 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.369+24C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 4/13 | chr19 | 327840 | |||||||
| chr19:327998 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(137): Show |
163 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.244-9C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 327998 | |||||||
| chr19:327999 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0001g0330 |
2 | NA18949.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.244-10C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 327999 | |||||||
| chr19:328028 | C | T | 31 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(28): Show |
32 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.244-39G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328028 | |||||||
| chr19:328118 | A | C | 1 | a0001c0006t0001g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.244-129T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328118 | |||||||
| chr19:328211 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.244-222C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328211 | |||||||
| chr19:328425 | G | GA | 6 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0208 others(3): Show |
6 | HG00741.hp2 HG01261.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-437dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328425 | |||||||
| chr19:328516 | A | G | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.244-527T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328516 | |||||||
| chr19:328564 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.244-575T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328564 | |||||||
| chr19:328569 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.244-580C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328569 | |||||||
| chr19:328577 | G | A | 26 | a0001c0001t0001g0237 a0001c0002t0002g0109 a0001c0002t0002g0110 others(23): Show |
26 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.244-588C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328577 | |||||||
| chr19:328621 | A | G | 51 | a0001c0001t0001g0237 a0001c0002t0001g0238 a0001c0002t0002g0109 others(48): Show |
53 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.244-632T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328621 | |||||||
| chr19:328656 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0093 others(2): Show |
6 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-667C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328656 | |||||||
| chr19:328666 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.244-677A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328666 | |||||||
| chr19:328762 | G | C | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG00673.hp1 HG01952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.244-773C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328762 | |||||||
| chr19:328855 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(137): Show |
164 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.244-866G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328855 | |||||||
| chr19:328936 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.244-947A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 328936 | |||||||
| chr19:329020 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.244-1031G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329020 | |||||||
| chr19:329073 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0076 |
4 | NA18946.hp2 NA18967.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-1084C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329073 | |||||||
| chr19:329109 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.244-1120G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329109 | |||||||
| chr19:329234 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.244-1245G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329234 | |||||||
| chr19:329255 | T | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0256 a0001c0017t0001g0097 |
3 | HG00099.hp1 HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.244-1266A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329255 | |||||||
| chr19:329335 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.244-1346A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329335 | |||||||
| chr19:329452 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0086 |
3 | HG02630.hp2 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.244-1463A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329452 | |||||||
| chr19:329493 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.244-1504T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329493 | |||||||
| chr19:329505 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.244-1516C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329505 | |||||||
| chr19:329532 | C | T | 3 | a0001c0002t0002g0240 a0001c0002t0002g0241 a0001c0002t0002g0243 |
3 | HG01109.hp1 HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.244-1543G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329532 | |||||||
| chr19:329601 | C | A | 5 | a0001c0005t0002g0013 a0001c0005t0002g0129 a0001c0005t0002g0130 others(2): Show |
6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-1612G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329601 | |||||||
| chr19:329703 | A | G | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.244-1714T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329703 | |||||||
| chr19:329746 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(53): Show |
66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.244-1757C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329746 | |||||||
| chr19:329781 | G | A | 27 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0105 others(24): Show |
29 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.244-1792C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329781 | |||||||
| chr19:329815 | G | A | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.244-1826C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329815 | |||||||
| chr19:329817 | C | G | 51 | a0001c0001t0001g0237 a0001c0002t0001g0238 a0001c0002t0002g0109 others(48): Show |
53 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.244-1828G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329817 | |||||||
| chr19:329841 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(188): Show |
217 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.244-1852T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329841 | |||||||
| chr19:329852 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.244-1863C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329852 | |||||||
| chr19:329866 | C | CA | 10 | a0001c0002t0002g0113 a0001c0002t0002g0114 a0001c0002t0002g0115 others(7): Show |
10 | HG01081.hp2 HG01175.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.244-1878dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | |||||||
| chr19:329866 | C | CAA | 7 | a0001c0001t0001g0237 a0001c0002t0002g0239 a0001c0002t0002g0240 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-1879_244-1878d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | |||||||
| chr19:329866 | CA | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(202): Show |
240 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.244-1878delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | |||||||
| chr19:329866 | CAA | C | 18 | a0001c0001t0001g0144 a0001c0001t0001g0167 a0001c0001t0001g0181 others(15): Show |
18 | HG00438.hp2 HG01106.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.244-1879_244-1878d others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | |||||||
| chr19:329866 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.244-1888_244-1878d others(13): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329866 | |||||||
| chr19:329885 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.244-1896T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 329885 | |||||||
| chr19:330123 | T | C | 1 | a0001c0001t0004g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.244-2134A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330123 | |||||||
| chr19:330263 | C | T | 50 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(47): Show |
52 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.244-2274G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330263 | |||||||
| chr19:330318 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.244-2329C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330318 | |||||||
| chr19:330328 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.244-2339G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330328 | |||||||
| chr19:330390 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.244-2401T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330390 | |||||||
| chr19:330426 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.244-2437C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330426 | |||||||
| chr19:330429 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.244-2440C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330429 | |||||||
| chr19:330467 | T | C | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.244-2478A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330467 | |||||||
| chr19:330505 | C | T | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.244-2516G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330505 | |||||||
| chr19:330533 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.244-2544G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330533 | |||||||
| chr19:330555 | G | GA | 13 | a0001c0001t0001g0091 a0001c0001t0001g0213 a0001c0001t0001g0223 others(10): Show |
13 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.244-2567dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330555 | |||||||
| chr19:330797 | C | T | 1 | a0001c0002t0002g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.244-2808G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330797 | |||||||
| chr19:330853 | T | C | 51 | a0001c0001t0001g0237 a0001c0002t0001g0238 a0001c0002t0002g0109 others(48): Show |
53 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.244-2864A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330853 | |||||||
| chr19:330854 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.244-2865C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330854 | |||||||
| chr19:330870 | C | T | 1 | a0001c0002t0002g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.244-2881G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330870 | |||||||
| chr19:330888 | C | T | 1 | a0001c0006t0003g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.244-2899G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 330888 | |||||||
| chr19:331028 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.244-3039C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331028 | |||||||
| chr19:331072 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.244-3083G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331072 | |||||||
| chr19:331124 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(188): Show |
217 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.244-3135A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331124 | |||||||
| chr19:331311 | T | C | 5 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(2): Show |
5 | HG01891.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+3089A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331311 | |||||||
| chr19:331360 | G | GAAAAAAA others(1): Show |
26 | a0001c0001t0001g0237 a0001c0002t0001g0238 a0001c0002t0002g0109 others(23): Show |
27 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.243+3032_243+3039d others(10): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | |||||||
| chr19:331360 | G | GAAAAAAA others(2): Show |
6 | a0001c0002t0002g0112 a0001c0002t0002g0116 a0001c0002t0002g0124 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+3031_243+3039d others(11): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | |||||||
| chr19:331360 | G | GAAAAAAA others(3): Show |
15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.243+3030_243+3039d others(12): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | |||||||
| chr19:331360 | G | GAAAAAAA others(4): Show |
2 | a0001c0003t0002g0163 a0001c0027t0001g0160 |
2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.243+3029_243+3039d others(13): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | |||||||
| chr19:331360 | G | GGAAAAAA others(3): Show |
2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.243+3039_243+3040i others(12): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331360 | |||||||
| chr19:331525 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.243+2875C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331525 | |||||||
| chr19:331748 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.243+2652G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331748 | |||||||
| chr19:331749 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.243+2651C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331749 | |||||||
| chr19:331810 | G | A | 1 | a0001c0007t0001g0175 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.243+2590C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331810 | |||||||
| chr19:331838 | G | A | 13 | a0001c0006t0001g0014 a0001c0006t0001g0137 a0001c0006t0003g0141 others(10): Show |
14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+2562C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331838 | |||||||
| chr19:331850 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.243+2550T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331850 | |||||||
| chr19:331896 | A | G | 56 | a0001c0001t0001g0012 a0001c0001t0001g0086 a0001c0001t0001g0093 others(53): Show |
59 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.243+2504T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331896 | |||||||
| chr19:331904 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(135): Show |
161 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.243+2496G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331904 | |||||||
| chr19:331908 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.243+2492C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331908 | |||||||
| chr19:331937 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0191 a0001c0001t0001g0213 others(2): Show |
6 | HG00438.hp2 HG00597.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+2463G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331937 | |||||||
| chr19:331972 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.243+2428G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 331972 | |||||||
| chr19:332058 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.243+2342A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332058 | |||||||
| chr19:332167 | G | C | 1 | a0001c0001t0001g0018 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.243+2233C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332167 | |||||||
| chr19:332219 | T | C | 2 | a0001c0013t0001g0257 a0001c0013t0001g0258 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.243+2181A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332219 | |||||||
| chr19:332377 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.243+2023T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332377 | |||||||
| chr19:332389 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.243+2011C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332389 | |||||||
| chr19:332431 | TGCTGGGA others(684): Show |
T | 5 | a0001c0005t0002g0013 a0001c0005t0002g0129 a0001c0005t0002g0130 others(2): Show |
6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+1278_243+1968d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332431 | |||||||
| chr19:332439 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.243+1961A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332439 | |||||||
| chr19:332459 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.243+1941C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332459 | |||||||
| chr19:332468 | ATTTTTGT others(689): Show |
A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(141): Show |
168 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.243+1236_243+1931d others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332468 | |||||||
| chr19:332490 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.243+1910G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332490 | |||||||
| chr19:332650 | A | G | 20 | a0001c0002t0001g0238 a0001c0003t0002g0015 a0001c0003t0002g0151 others(17): Show |
21 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.243+1750T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332650 | |||||||
| chr19:332814 | ATTTTTTT others(690): Show |
A | 1 | a0001c0001t0001g0320 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.243+889_243+1585de others(1): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332814 | |||||||
| chr19:332823 | A | T | 45 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(42): Show |
46 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.243+1577T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332823 | |||||||
| chr19:332824 | ATTTTTTT others(690): Show |
A | 46 | a0001c0001t0001g0308 a0001c0002t0001g0238 a0001c0002t0002g0109 others(43): Show |
47 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.243+879_243+1575de others(1): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332824 | |||||||
| chr19:332904 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18991.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.243+1496C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 332904 | |||||||
| chr19:333015 | C | T | 1 | a0001c0001t0012g0071 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.243+1385G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333015 | |||||||
| chr19:333180 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(74): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.243+1220A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333180 | |||||||
| chr19:333198 | A | G | 2 | a0002c0004t0003g0135 a0002c0004t0003g0138 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.243+1202T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333198 | |||||||
| chr19:333520 | A | AT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0034 others(3): Show |
10 | HG00280.hp1 HG00738.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+879dupA | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333520 | |||||||
| chr19:333552 | C | T | 2 | a0001c0002t0002g0246 a0002c0015t0003g0247 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.243+848G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333552 | |||||||
| chr19:333558 | G | A | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0288 others(1): Show |
4 | NA18950.hp2 NA18965.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+842C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333558 | |||||||
| chr19:333582 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.243+818G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333582 | |||||||
| chr19:333583 | G | A | 1 | a0001c0002t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.243+817C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333583 | |||||||
| chr19:333696 | T | A | 45 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(42): Show |
46 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.243+704A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333696 | |||||||
| chr19:333712 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.243+688C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333712 | |||||||
| chr19:333713 | G | A | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+687C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333713 | |||||||
| chr19:333734 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.243+666C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333734 | |||||||
| chr19:333751 | C | T | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.243+649G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333751 | |||||||
| chr19:333752 | G | A | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.243+648C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333752 | |||||||
| chr19:333775 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.243+625C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333775 | |||||||
| chr19:333849 | C | T | 25 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(22): Show |
25 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.243+551G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333849 | |||||||
| chr19:333893 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.243+507G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333893 | |||||||
| chr19:333907 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
297 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.243+493G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333907 | |||||||
| chr19:333918 | T | A | 1 | a0003c0012t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.243+482A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333918 | |||||||
| chr19:333932 | T | C | 1 | a0001c0002t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.243+468A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333932 | |||||||
| chr19:333937 | G | C | 2 | a0001c0005t0002g0244 a0001c0005t0002g0245 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.243+463C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 333937 | |||||||
| chr19:334087 | A | C | 1 | a0001c0005t0002g0244 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.243+313T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 334087 | |||||||
| chr19:334170 | CAGA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(126): Show |
152 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.243+227_243+229del others(3): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 334170 | |||||||
| chr19:334360 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.243+40G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 3/13 | chr19 | 334360 | |||||||
| chr19:334673 | G | A | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 |
3 | NA19005.hp1 NA19056.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.101-131C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334673 | |||||||
| chr19:334716 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.101-174C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334716 | |||||||
| chr19:334756 | G | T | 61 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(58): Show |
71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.101-214C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334756 | |||||||
| chr19:334935 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.101-393C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334935 | |||||||
| chr19:334936 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.101-394A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 334936 | |||||||
| chr19:335047 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.101-505A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335047 | |||||||
| chr19:335055 | A | C | 63 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(60): Show |
66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.101-513T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335055 | |||||||
| chr19:335061 | G | T | 1 | a0001c0001t0001g0298 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.101-519C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335061 | |||||||
| chr19:335202 | A | AT | 38 | a0001c0002t0001g0238 a0001c0003t0002g0015 a0001c0003t0002g0151 others(35): Show |
41 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.101-661dupA | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335202 | |||||||
| chr19:335267 | C | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(256): Show |
296 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.101-725G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335267 | |||||||
| chr19:335338 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02056.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.100+745G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335338 | |||||||
| chr19:335352 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0180 |
3 | HG02257.hp1 HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.100+731C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335352 | |||||||
| chr19:335393 | G | C | 2 | a0001c0001t0004g0061 a0001c0001t0004g0073 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.100+690C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335393 | |||||||
| chr19:335488 | C | T | 1 | a0002c0004t0003g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+595G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335488 | |||||||
| chr19:335546 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.100+537G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335546 | |||||||
| chr19:335606 | G | A | 2 | a0001c0002t0002g0117 a0001c0002t0002g0120 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.100+477C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335606 | |||||||
| chr19:335673 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(154): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.100+410C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335673 | |||||||
| chr19:335724 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.100+359C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335724 | |||||||
| chr19:335726 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.100+357G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335726 | |||||||
| chr19:335808 | G | A | 1 | a0001c0001t0007g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100+275C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335808 | |||||||
| chr19:335817 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.100+266C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335817 | |||||||
| chr19:335907 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.100+176C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335907 | |||||||
| chr19:335946 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(178): Show |
212 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.100+137C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335946 | |||||||
| chr19:335967 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.100+116C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 2/13 | chr19 | 335967 | |||||||
| chr19:336279 | T | G | 63 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(60): Show |
66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.10-106A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336279 | |||||||
| chr19:336316 | T | C | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.10-143A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336316 | |||||||
| chr19:336350 | G | A | 63 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(60): Show |
66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.10-177C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336350 | |||||||
| chr19:336379 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.10-206C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336379 | |||||||
| chr19:336396 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.10-223C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336396 | |||||||
| chr19:336505 | A | G | 63 | a0001c0001t0001g0237 a0001c0002t0001g0238 a0001c0002t0002g0109 others(60): Show |
66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.10-332T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336505 | |||||||
| chr19:336550 | T | C | 1 | a0001c0017t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.10-377A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336550 | |||||||
| chr19:336854 | T | C | 18 | a0001c0005t0002g0013 a0001c0005t0002g0129 a0001c0005t0002g0130 others(15): Show |
20 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.10-681A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336854 | |||||||
| chr19:336881 | C | T | 26 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(23): Show |
26 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.10-708G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336881 | |||||||
| chr19:336911 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
295 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.10-738A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336911 | |||||||
| chr19:336932 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(258): Show |
298 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.10-759T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 336932 | |||||||
| chr19:337007 | T | G | 1 | a0001c0001t0001g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.10-834A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337007 | |||||||
| chr19:337212 | A | C | 62 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(59): Show |
65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-1039T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337212 | |||||||
| chr19:337247 | C | T | 63 | a0001c0001t0007g0092 a0001c0002t0001g0238 a0001c0002t0002g0109 others(60): Show |
66 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.10-1074G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337247 | |||||||
| chr19:337291 | T | C | 3 | a0001c0001t0001g0263 a0001c0001t0001g0280 a0001c0001t0001g0293 |
3 | HG01257.hp1 HG01496.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.10-1118A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337291 | |||||||
| chr19:337315 | A | C | 1 | a0001c0001t0001g0296 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.10-1142T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337315 | |||||||
| chr19:337333 | C | T | 13 | a0001c0006t0001g0014 a0001c0006t0001g0137 a0001c0006t0003g0141 others(10): Show |
14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.10-1160G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337333 | |||||||
| chr19:337641 | C | T | 62 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(59): Show |
65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-1468G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337641 | |||||||
| chr19:337790 | A | G | 5 | a0001c0005t0002g0013 a0001c0005t0002g0129 a0001c0005t0002g0130 others(2): Show |
6 | HG01891.hp1 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-1617T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337790 | |||||||
| chr19:337800 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.10-1627G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337800 | |||||||
| chr19:337801 | G | A | 14 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(11): Show |
15 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.10-1628C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337801 | |||||||
| chr19:337806 | C | T | 62 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(59): Show |
65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-1633G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337806 | |||||||
| chr19:337870 | C | CA | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
205 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.10-1698dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | |||||||
| chr19:337870 | C | CAA | 32 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(29): Show |
32 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.10-1699_10-1698dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | |||||||
| chr19:337870 | C | CAAAAA | 17 | a0001c0003t0002g0151 a0001c0003t0002g0153 a0001c0003t0002g0154 others(14): Show |
17 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.10-1702_10-1698dup others(5): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | |||||||
| chr19:337870 | C | CAAAAAA | 14 | a0001c0003t0002g0015 a0001c0003t0002g0152 a0001c0003t0002g0161 others(11): Show |
16 | HG01361.hp2 HG01884.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.10-1703_10-1698dup others(6): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | |||||||
| chr19:337870 | C | CAAAAAAA others(2): Show |
13 | a0001c0002t0002g0109 a0001c0002t0002g0111 a0001c0002t0002g0113 others(10): Show |
14 | HG01081.hp2 HG02300.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.10-1706_10-1698dup others(9): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | |||||||
| chr19:337870 | C | CAAAAAAA others(3): Show |
11 | a0001c0002t0002g0110 a0001c0002t0002g0112 a0001c0002t0002g0118 others(8): Show |
11 | HG01109.hp1 HG01891.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.10-1707_10-1698dup others(10): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | |||||||
| chr19:337870 | C | CAAAAAAA others(4): Show |
4 | a0001c0002t0002g0121 a0001c0002t0002g0122 a0001c0002t0002g0241 others(1): Show |
4 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-1708_10-1698dup others(11): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337870 | |||||||
| chr19:337912 | G | T | 68 | a0001c0001t0001g0005 a0001c0001t0001g0087 a0001c0001t0001g0088 others(65): Show |
73 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.10-1739C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337912 | |||||||
| chr19:337928 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.10-1755G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337928 | |||||||
| chr19:337942 | G | C | 62 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(59): Show |
65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-1769C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337942 | |||||||
| chr19:337989 | A | C | 2 | a0001c0003t0002g0185 a0005c0025t0001g0184 |
2 | NA18951.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.10-1816T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 337989 | |||||||
| chr19:338001 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.10-1828C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338001 | |||||||
| chr19:338042 | G | T | 2 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.10-1869C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338042 | |||||||
| chr19:338059 | T | C | 2 | a0001c0008t0001g0068 a0001c0008t0001g0075 |
2 | NA18989.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.10-1886A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338059 | |||||||
| chr19:338170 | CA | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.10-1998delT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | |||||||
| chr19:338170 | CAA | C | 17 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
18 | HG00738.hp1 HG01167.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.10-1999_10-1998del others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | |||||||
| chr19:338170 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0002g0123 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.10-2008_10-1998del others(11): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | |||||||
| chr19:338170 | CAAAAAAA others(5): Show |
C | 47 | a0001c0001t0001g0165 a0001c0002t0001g0238 a0001c0002t0002g0109 others(44): Show |
49 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.10-2009_10-1998del others(12): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | |||||||
| chr19:338170 | CAAAAAAA others(6): Show |
C | 15 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(12): Show |
16 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.10-2010_10-1998del others(13): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | |||||||
| chr19:338170 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0025 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.10-2012_10-1998del others(15): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338170 | |||||||
| chr19:338229 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.10-2056C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338229 | |||||||
| chr19:338408 | CTGAG | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(16): Show |
22 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.10-2239_10-2236del others(4): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338408 | |||||||
| chr19:338437 | G | T | 1 | a0001c0006t0003g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.10-2264C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338437 | |||||||
| chr19:338533 | C | T | 1 | a0001c0002t0002g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10-2360G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338533 | |||||||
| chr19:338568 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0261 |
4 | NA18949.hp2 NA18972.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.10-2395G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338568 | |||||||
| chr19:338576 | G | A | 2 | a0001c0002t0002g0111 a0001c0002t0002g0112 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-2403C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338576 | |||||||
| chr19:338581 | C | CA | 62 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(59): Show |
65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-2409dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338581 | |||||||
| chr19:338582 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.10-2409T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338582 | |||||||
| chr19:338693 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(15): Show |
21 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.10-2520C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338693 | |||||||
| chr19:338719 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.10-2546C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338719 | |||||||
| chr19:338944 | C | T | 62 | a0001c0002t0001g0238 a0001c0002t0002g0109 a0001c0002t0002g0110 others(59): Show |
65 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.10-2771G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 338944 | |||||||
| chr19:339079 | C | CA | 70 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(67): Show |
73 | HG00423.hp1 HG01071.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.10-2907dupT | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339079 | |||||||
| chr19:339079 | C | CAA | 6 | a0001c0002t0002g0124 a0001c0002t0002g0243 a0001c0003t0002g0163 others(3): Show |
6 | HG01109.hp1 HG01361.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-2908_10-2907dup others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339079 | |||||||
| chr19:339134 | T | C | 3 | a0002c0004t0003g0133 a0002c0004t0003g0142 a0002c0004t0003g0143 |
3 | HG02257.hp2 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.10-2961A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339134 | |||||||
| chr19:339186 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(68): Show |
87 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.10-3013C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339186 | |||||||
| chr19:339228 | T | G | 13 | a0001c0006t0001g0014 a0001c0006t0001g0137 a0001c0006t0003g0141 others(10): Show |
14 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.10-3055A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339228 | |||||||
| chr19:339372 | C | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.10-3199G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339372 | |||||||
| chr19:339533 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.10-3360A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339533 | |||||||
| chr19:339675 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(70): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.10-3502G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339675 | |||||||
| chr19:339677 | C | T | 16 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(13): Show |
17 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.10-3504G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339677 | |||||||
| chr19:339795 | G | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0233 a0001c0001t0001g0234 |
4 | HG01928.hp1 HG01943.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-3622C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339795 | |||||||
| chr19:339804 | G | C | 16 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(13): Show |
17 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.10-3631C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339804 | |||||||
| chr19:339812 | A | G | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.10-3639T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339812 | |||||||
| chr19:339905 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
9 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.10-3732G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339905 | |||||||
| chr19:339955 | G | A | 1 | a0002c0004t0003g0106 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.10-3782C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 339955 | |||||||
| chr19:340055 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.10-3882A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340055 | |||||||
| chr19:340158 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.10-3985G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340158 | |||||||
| chr19:340193 | C | G | 2 | a0001c0003t0002g0151 a0001c0003t0002g0152 |
2 | NA18961.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.10-4020G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340193 | |||||||
| chr19:340225 | A | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.10-4052T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340225 | |||||||
| chr19:340286 | C | T | 1 | a0002c0004t0003g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.10-4113G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340286 | |||||||
| chr19:340350 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.10-4177C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340350 | |||||||
| chr19:340355 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.10-4182A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340355 | |||||||
| chr19:340386 | C | T | 3 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 |
3 | HG02896.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.10-4213G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340386 | |||||||
| chr19:340652 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.9+4122T>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340652 | |||||||
| chr19:340671 | G | A | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+4103C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340671 | |||||||
| chr19:340700 | C | T | 139 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.9+4074G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340700 | |||||||
| chr19:340960 | T | A | 1 | a0001c0002t0002g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9+3814A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 340960 | |||||||
| chr19:341037 | C | T | 14 | a0001c0003t0002g0015 a0001c0003t0002g0151 a0001c0003t0002g0152 others(11): Show |
15 | HG01071.hp2 HG01106.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.9+3737G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341037 | |||||||
| chr19:341087 | G | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(188): Show |
217 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.9+3687C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341087 | |||||||
| chr19:341161 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0080 |
3 | HG02074.hp2 HG02132.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.9+3613A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341161 | |||||||
| chr19:341174 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.9+3600C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341174 | |||||||
| chr19:341288 | A | G | 32 | a0001c0001t0001g0237 a0001c0002t0001g0238 a0001c0002t0002g0109 others(29): Show |
33 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.9+3486T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341288 | |||||||
| chr19:341392 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0016 others(136): Show |
162 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.9+3382G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341392 | |||||||
| chr19:341455 | G | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(16): Show |
22 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.9+3319C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341455 | |||||||
| chr19:341462 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3312G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341462 | |||||||
| chr19:341463 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3311G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341463 | |||||||
| chr19:341477 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3297G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341477 | |||||||
| chr19:341495 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3279G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341495 | |||||||
| chr19:341498 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3276G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341498 | |||||||
| chr19:341500 | A | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(49): Show |
56 | HG00099.hp1 HG00639.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.9+3274T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341500 | |||||||
| chr19:341502 | T | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3272A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341502 | |||||||
| chr19:341503 | T | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3271A>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341503 | |||||||
| chr19:341513 | G | A | 1 | a0009c0026t0002g0128 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.9+3261C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341513 | |||||||
| chr19:341513 | GCGACTCT others(19): Show |
G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3235_9+3260delTG others(24): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341513 | |||||||
| chr19:341615 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3159G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341615 | |||||||
| chr19:341650 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3124G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341650 | |||||||
| chr19:341651 | A | C | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3123T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341651 | |||||||
| chr19:341652 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3122G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341652 | |||||||
| chr19:341667 | T | C | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3107A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341667 | |||||||
| chr19:341668 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3106G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341668 | |||||||
| chr19:341669 | T | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3105A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341669 | |||||||
| chr19:341672 | G | C | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3102C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341672 | |||||||
| chr19:341674 | T | C | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3100A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341674 | |||||||
| chr19:341675 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+3099G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341675 | |||||||
| chr19:341730 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.9+3044C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341730 | |||||||
| chr19:341803 | T | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2971A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341803 | |||||||
| chr19:341831 | G | A | 3 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 |
3 | HG02896.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.9+2943C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341831 | |||||||
| chr19:341845 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2929G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341845 | |||||||
| chr19:341894 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.9+2880T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341894 | |||||||
| chr19:341899 | A | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.9+2875T>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341899 | |||||||
| chr19:341918 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2856G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341918 | |||||||
| chr19:341919 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2855G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341919 | |||||||
| chr19:341922 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2852G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341922 | |||||||
| chr19:341923 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2851G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341923 | |||||||
| chr19:341924 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2850G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341924 | |||||||
| chr19:341926 | T | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2848A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341926 | |||||||
| chr19:341927 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2847G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341927 | |||||||
| chr19:341928 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2846G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341928 | |||||||
| chr19:341929 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2845G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341929 | |||||||
| chr19:341930 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2844G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341930 | |||||||
| chr19:341931 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2843G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341931 | |||||||
| chr19:341935 | G | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2839C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341935 | |||||||
| chr19:341936 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2838G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341936 | |||||||
| chr19:341939 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2835G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341939 | |||||||
| chr19:341940 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2834G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341940 | |||||||
| chr19:341941 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2833G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341941 | |||||||
| chr19:341942 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2832G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341942 | |||||||
| chr19:341943 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2831G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341943 | |||||||
| chr19:341944 | A | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2830T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341944 | |||||||
| chr19:341945 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2829G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341945 | |||||||
| chr19:341946 | A | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2828T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341946 | |||||||
| chr19:341949 | T | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2825A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341949 | |||||||
| chr19:341981 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.9+2793G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341981 | |||||||
| chr19:341996 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(18): Show |
24 | HG00099.hp1 HG00639.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.9+2778G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 341996 | |||||||
| chr19:342006 | G | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2768C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342006 | |||||||
| chr19:342024 | G | A | 2 | a0001c0002t0002g0246 a0002c0015t0003g0247 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.9+2750C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342024 | |||||||
| chr19:342029 | G | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2745C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342029 | |||||||
| chr19:342034 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2740G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342034 | |||||||
| chr19:342044 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2730G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342044 | |||||||
| chr19:342046 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2728G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342046 | |||||||
| chr19:342048 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2726G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342048 | |||||||
| chr19:342049 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2725G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342049 | |||||||
| chr19:342050 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2724G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342050 | |||||||
| chr19:342055 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2719G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342055 | |||||||
| chr19:342056 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2718G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342056 | |||||||
| chr19:342063 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2711G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342063 | |||||||
| chr19:342065 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2709G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342065 | |||||||
| chr19:342066 | T | C | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2708A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342066 | |||||||
| chr19:342067 | C | A | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2707G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342067 | |||||||
| chr19:342068 | C | G | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2706G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342068 | |||||||
| chr19:342069 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2705G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342069 | |||||||
| chr19:342070 | C | T | 1 | a0001c0001t0005g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.9+2704G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342070 | |||||||
| chr19:342119 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
9 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+2655G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342119 | |||||||
| chr19:342188 | T | C | 1 | a0001c0001t0002g0023 | 2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.9+2586A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342188 | |||||||
| chr19:342331 | A | G | 39 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(36): Show |
44 | HG00099.hp1 HG00639.hp2 HG01516.hp1 others(41): Show |
intron_variant | MODIFIER | c.9+2443T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342331 | |||||||
| chr19:342355 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.9+2419A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342355 | |||||||
| chr19:342394 | G | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG02083.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.9+2380C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342394 | |||||||
| chr19:342445 | C | G | 20 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0002t0002g0109 others(17): Show |
20 | HG00639.hp1 HG00738.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.9+2329G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342445 | |||||||
| chr19:342474 | A | G | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+2300T>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342474 | |||||||
| chr19:342556 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(15): Show |
21 | HG00099.hp1 HG00639.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.9+2218C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342556 | |||||||
| chr19:342558 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.9+2216C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342558 | |||||||
| chr19:342617 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.9+2157G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 342617 | |||||||
| chr19:343020 | C | G | 3 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 |
3 | HG02896.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.9+1754G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343020 | |||||||
| chr19:343081 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0330 |
2 | HG01255.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.9+1693C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343081 | |||||||
| chr19:343093 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18991.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.9+1681C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343093 | |||||||
| chr19:343215 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9+1559G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343215 | |||||||
| chr19:343379 | C | T | 2 | a0001c0013t0001g0257 a0001c0013t0001g0258 |
2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.9+1395G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343379 | |||||||
| chr19:343383 | C | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.9+1391G>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343383 | |||||||
| chr19:343475 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.9+1299C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343475 | |||||||
| chr19:343546 | C | G | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+1228G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343546 | |||||||
| chr19:343828 | C | T | 4 | a0001c0002t0002g0109 a0001c0002t0002g0110 a0001c0002t0002g0111 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+946G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343828 | |||||||
| chr19:343830 | C | T | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+944G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343830 | |||||||
| chr19:343973 | G | GT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+800dupA | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 343973 | |||||||
| chr19:344005 | C | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(18): Show |
24 | HG00099.hp1 HG00639.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.9+769G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344005 | |||||||
| chr19:344010 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.9+764C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344010 | |||||||
| chr19:344030 | T | G | 3 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 |
3 | HG02896.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.9+744A>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344030 | |||||||
| chr19:344053 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.9+721A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344053 | |||||||
| chr19:344079 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.9+695G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344079 | |||||||
| chr19:344100 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.9+674C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344100 | |||||||
| chr19:344211 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.9+563G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344211 | |||||||
| chr19:344299 | G | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(56): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.9+475C>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344299 | |||||||
| chr19:344448 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.9+326G>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344448 | |||||||
| chr19:344520 | C | G | 1 | a0002c0004t0003g0106 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.9+254G>C | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344520 | |||||||
| chr19:344522 | G | A | 31 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0105 others(28): Show |
34 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.9+252C>T | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344522 | |||||||
| chr19:344568 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.9+206C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344568 | |||||||
| chr19:344586 | C | CGGGCCG | 21 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0086 others(18): Show |
24 | HG00099.hp1 HG00438.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.9+187_9+188insCGGC others(2): Show |
MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344586 | |||||||
| chr19:344606 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.9+168A>G | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344606 | |||||||
| chr19:344644 | G | T | 2 | a0001c0014t0002g0032 a0001c0014t0002g0033 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+130C>A | MIER2 | ENSG00000105556.12 | transcript | ENST00000264819.7 | protein_coding | 1/13 | chr19 | 344644 |