| geneid | 22877 |
|---|---|
| ensemblid | ENSG00000175727.15 |
| hgncid | 17055 |
| symbol | MLXIP |
| name | MLX interacting protein |
| refseq_nuc | NM_014938.6 |
| refseq_prot | NP_055753.3 |
| ensembl_nuc | ENST00000319080.12 |
| ensembl_prot | ENSP00000312834.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 122078756 |
| end | 122147344 |
| strand | + |
| ver | v1.2 |
| region | chr12:122078756-122147344 |
| region5000 | chr12:122073756-122152344 |
| regionname0 | MLXIP_chr12_122078756_122147344 |
| regionname5000 | MLXIP_chr12_122073756_122152344 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 919 | 184 | 25 | 50 | 73 | 9 | 26 | 55 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002 | 0/1 | 919 | 145 | 42 | 21 | 60 | 5 | 16 | 43 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0003 | 0/0 | 919 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0004 | 0/0 | 919 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0005 | 0/0 | 919 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0006 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0007 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0008 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0009 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0010 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0011 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0012 | 0/0 | 914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0013 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0014 | 0/0 | 919 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0015 | 0/0 | 919 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2760 | 136 | 20 | 34 | 52 | 5 | 24 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0002 | 0/0 | 2760 | 78 | 18 | 12 | 39 | 1 | 8 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0003 | 0/0 | 2760 | 43 | 2 | 16 | 20 | 3 | 2 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0004 | 0/0 | 2760 | 41 | 15 | 3 | 17 | 0 | 6 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0005 | 0/1 | 2760 | 12 | 0 | 6 | 0 | 3 | 2 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0006 | 0/0 | 2760 | 7 | 7 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0007 | 0/0 | 2760 | 5 | 4 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0008 | 0/0 | 2760 | 4 | 3 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0009 | 0/0 | 2760 | 4 | 2 | 0 | 1 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0010 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0011 | 0/0 | 2760 | 3 | 0 | 0 | 3 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0012 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0013 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0014 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0015 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0016 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0017 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0018 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0019 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0020 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0021 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0022 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0023 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0024 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0025 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0026 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| c0027 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5629 | 71 | 12 | 14 | 24 | 6 | 15 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0002 | 0/0 | 5621 | 49 | 5 | 11 | 29 | 1 | 3 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0003 | 0/0 | 5629 | 47 | 7 | 15 | 17 | 3 | 5 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0004 | 0/0 | 5629 | 14 | 0 | 2 | 10 | 1 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0005 | 0/0 | 5609 | 14 | 8 | 2 | 3 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0006 | 0/0 | 5629 | 11 | 0 | 1 | 10 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0007 | 0/0 | 5630 | 9 | 0 | 1 | 7 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0008 | 0/0 | 5629 | 8 | 0 | 7 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0009 | 0/1 | 5629 | 6 | 0 | 3 | 0 | 1 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0010 | 0/0 | 5630 | 6 | 0 | 0 | 6 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0011 | 0/0 | 5629 | 6 | 5 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0012 | 0/0 | 5625 | 5 | 5 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0013 | 0/0 | 5631 | 5 | 5 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0014 | 0/0 | 5630 | 5 | 0 | 1 | 3 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0015 | 0/0 | 5628 | 5 | 1 | 2 | 1 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0016 | 0/0 | 5621 | 4 | 0 | 2 | 1 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0017 | 0/0 | 5621 | 4 | 4 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0018 | 0/0 | 5631 | 4 | 0 | 3 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0019 | 0/0 | 5626 | 3 | 2 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0020 | 0/0 | 5630 | 3 | 2 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0021 | 0/0 | 5629 | 3 | 2 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0022 | 0/0 | 5627 | 3 | 0 | 0 | 0 | 0 | 3 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0023 | 0/0 | 5621 | 2 | 0 | 0 | 2 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0024 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0025 | 0/0 | 5628 | 2 | 0 | 0 | 2 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0026 | 0/0 | 5621 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0027 | 0/0 | 5632 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0028 | 0/0 | 5630 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0029 | 0/0 | 5630 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0030 | 0/0 | 5629 | 2 | 0 | 2 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0031 | 0/0 | 5629 | 2 | 0 | 0 | 2 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0032 | 0/0 | 5629 | 2 | 0 | 0 | 1 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0033 | 0/0 | 5630 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0034 | 0/0 | 5631 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0035 | 0/0 | 5621 | 2 | 0 | 0 | 0 | 0 | 2 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0036 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0037 | 0/0 | 5631 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0038 | 0/0 | 5621 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0039 | 0/0 | 5621 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0040 | 0/0 | 5621 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0041 | 0/0 | 5621 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0042 | 0/0 | 5630 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0043 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0044 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0045 | 0/0 | 5621 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0046 | 0/0 | 5630 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0047 | 0/0 | 5630 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0048 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0049 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0050 | 0/0 | 5629 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0051 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0052 | 0/0 | 5629 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0053 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0054 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0055 | 0/0 | 5621 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0056 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0057 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0058 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0059 | 0/0 | 5628 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0060 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0061 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0062 | 0/0 | 5629 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0063 | 1/0 | 5631 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0064 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0065 | 0/0 | 5628 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0066 | 0/0 | 5609 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0067 | 0/0 | 5609 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0068 | 0/0 | 5609 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0069 | 0/0 | 5608 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0070 | 0/0 | 5629 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0071 | 0/0 | 5629 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0072 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0073 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0074 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0075 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0076 | 0/0 | 5631 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0077 | 0/0 | 5619 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| t0078 | 0/0 | 5629 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2760 | 136 | 20 | 34 | 52 | 5 | 24 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003 | 0/0 | 2760 | 43 | 2 | 16 | 20 | 3 | 2 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0008 | 0/0 | 2760 | 4 | 3 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0019 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002 | 0/0 | 2760 | 78 | 18 | 12 | 39 | 1 | 8 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004 | 0/0 | 2760 | 41 | 15 | 3 | 17 | 0 | 6 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0005 | 0/1 | 2760 | 12 | 0 | 6 | 0 | 3 | 2 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0009 | 0/0 | 2760 | 4 | 2 | 0 | 1 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0010 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0011 | 0/0 | 2760 | 3 | 0 | 0 | 3 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0024 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0026 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0027 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0003c0006 | 0/0 | 2760 | 7 | 7 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0003c0018 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0004c0007 | 0/0 | 2760 | 5 | 4 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0005c0012 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0006c0025 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0007c0014 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0008c0020 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0009c0015 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0010c0016 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0011c0017 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0012c0022 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0013c0021 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0014c0023 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0015c0013 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8388 | 61 | 6 | 14 | 22 | 4 | 15 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0006 | 0/0 | 8388 | 11 | 0 | 1 | 10 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0007 | 0/0 | 8389 | 8 | 0 | 1 | 6 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0008 | 0/0 | 8388 | 8 | 0 | 7 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0011 | 0/0 | 8388 | 5 | 4 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0013 | 0/0 | 8390 | 5 | 5 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0014 | 0/0 | 8389 | 5 | 0 | 1 | 3 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0015 | 0/0 | 8387 | 4 | 0 | 2 | 1 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0018 | 0/0 | 8390 | 4 | 0 | 3 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0022 | 0/0 | 8386 | 3 | 0 | 0 | 0 | 0 | 3 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0029 | 0/0 | 8389 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0030 | 0/0 | 8388 | 2 | 0 | 2 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0031 | 0/0 | 8388 | 2 | 0 | 0 | 2 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0032 | 0/0 | 8388 | 2 | 0 | 0 | 1 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0033 | 0/0 | 8389 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0036 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0043 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0044 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0058 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0059 | 0/0 | 8387 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0060 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0062 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0063 | 1/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0064 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0065 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0071 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0001t0078 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003t0003 | 0/0 | 8388 | 35 | 1 | 15 | 15 | 3 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003t0004 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003t0007 | 0/0 | 8389 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003t0020 | 0/0 | 8389 | 2 | 1 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003t0025 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003t0047 | 0/0 | 8389 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003t0050 | 0/0 | 8388 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0003t0052 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0008t0028 | 0/0 | 8389 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0008t0048 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0008t0056 | 0/0 | 8384 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0001c0019t0001 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0002 | 0/0 | 8380 | 45 | 4 | 9 | 28 | 1 | 3 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0005 | 0/0 | 8368 | 3 | 3 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0010 | 0/0 | 8389 | 6 | 0 | 0 | 6 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0012 | 0/0 | 8384 | 5 | 5 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0016 | 0/0 | 8380 | 3 | 0 | 2 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0021 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0023 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0026 | 0/0 | 8380 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0027 | 0/0 | 8391 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0035 | 0/0 | 8380 | 2 | 0 | 0 | 0 | 0 | 2 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0038 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0039 | 0/0 | 8380 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0040 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0041 | 0/0 | 8380 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0042 | 0/0 | 8389 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0045 | 0/0 | 8380 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0055 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0002t0072 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0003 | 0/0 | 8388 | 8 | 4 | 0 | 0 | 0 | 4 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0004 | 0/0 | 8388 | 9 | 0 | 0 | 9 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0005 | 0/0 | 8368 | 11 | 5 | 2 | 3 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0020 | 0/0 | 8389 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0021 | 0/0 | 8388 | 2 | 1 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0024 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0049 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0053 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0054 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0057 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0066 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0067 | 0/0 | 8368 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0068 | 0/0 | 8368 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0004t0069 | 0/0 | 8367 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0005t0004 | 0/0 | 8388 | 4 | 0 | 2 | 0 | 1 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0005t0009 | 0/1 | 8388 | 6 | 0 | 3 | 0 | 1 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0005t0046 | 0/0 | 8389 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0005t0051 | 0/0 | 8388 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0009t0001 | 0/0 | 8388 | 2 | 0 | 0 | 1 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0009t0011 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0009t0070 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0010t0017 | 0/0 | 8380 | 4 | 4 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0011t0002 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0011t0016 | 0/0 | 8380 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0011t0037 | 0/0 | 8390 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0024t0002 | 0/0 | 8380 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0026t0003 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0002c0027t0003 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0003c0006t0001 | 0/0 | 8388 | 6 | 6 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0003c0006t0015 | 0/0 | 8387 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0003c0018t0061 | 0/0 | 8388 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0004c0007t0019 | 0/0 | 8385 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0004c0007t0034 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0004c0007t0075 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0004c0007t0076 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0005c0012t0073 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0005c0012t0074 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0006c0025t0025 | 0/0 | 8387 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0007c0014t0019 | 0/0 | 8385 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0008c0020t0019 | 0/0 | 8385 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0009c0015t0003 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0010c0016t0003 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0011c0017t0001 | 0/0 | 8388 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0012c0022t0023 | 0/0 | 8365 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0013c0021t0077 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0014c0023t0002 | 0/0 | 8380 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| a0015c0013t0002 | 0/0 | 8380 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | copy fasta | chr12 | 122073756 | 122152344 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0007g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0007g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0008g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0008g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0011g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0013g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0014g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0014g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0014g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0014g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0015g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0015g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0015g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0015g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0018g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0018g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0018g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0018g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0022g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0022g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0022g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0029g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0029g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0030g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0030g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0031g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0031g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0032g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0032g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0033g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0033g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0036g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0043g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0044g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0058g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0059g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0060g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0062g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0063g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0064g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0065g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0071g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0001t0078g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0020g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0020g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0025g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0047g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0050g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0003t0052g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0008t0028g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0008t0028g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0008t0048g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0008t0056g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0001c0019t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0010g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0010g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0010g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0010g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0012g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0016g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0016g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0016g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0021g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0023g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0026g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0026g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0027g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0027g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0035g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0035g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0038g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0039g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0040g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0041g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0042g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0045g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0055g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0002t0072g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0021g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0021g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0024g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0024g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0049g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0053g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0054g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0057g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0066g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0067g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0068g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0004t0069g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0009g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0009g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0009g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0009g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0009g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0046g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0005t0051g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0009t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0009t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0009t0070g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0010t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0010t0017g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0010t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0010t0017g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0011t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0011t0016g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0011t0037g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0024t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0026t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0002c0027t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0003c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0003c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0003c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0003c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0003c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0003c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0003c0006t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0003c0018t0061g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0004c0007t0019g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0004c0007t0034g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0004c0007t0034g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0004c0007t0075g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0004c0007t0076g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0005c0012t0073g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0005c0012t0074g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0006c0025t0025g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0007c0014t0019g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0008c0020t0019g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0009c0015t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0010c0016t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0011c0017t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0012c0022t0023g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0013c0021t0077g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0014c0023t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| a0015c0013t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0003 | g0314 | EUR | GBR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00140 | hp1 | a0001 | c0001 | t0018 | g0140 | EUR | GBR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00280 | hp2 | a0001 | c0003 | t0003 | g0321 | EUR | FIN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00323 | hp1 | a0002 | c0005 | t0009 | g0242 | EUR | FIN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0344 | EUR | FIN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00544 | hp1 | a0002 | c0002 | t0038 | g0221 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0134 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00558 | hp2 | a0002 | c0011 | t0016 | g0249 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00597 | hp2 | a0001 | c0008 | t0048 | g0295 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00609 | hp2 | a0001 | c0001 | t0078 | g0129 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00621 | hp1 | a0001 | c0001 | t0036 | g0098 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00621 | hp2 | a0002 | c0002 | t0072 | g0019 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00673 | hp1 | a0001 | c0003 | t0003 | g0302 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0167 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0087 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0320 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01069 | hp1 | a0002 | c0005 | t0004 | g0239 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0165 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01070 | hp1 | a0001 | c0003 | t0003 | g0310 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0199 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01071 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0166 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01074 | hp1 | a0001 | c0003 | t0050 | g0312 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0198 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0073 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01099 | hp1 | a0002 | c0005 | t0009 | g0243 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01099 | hp2 | a0004 | c0007 | t0019 | g0339 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01106 | hp1 | a0001 | c0001 | t0008 | g0141 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01109 | hp1 | a0002 | c0005 | t0009 | g0238 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01109 | hp2 | a0015 | c0013 | t0002 | g0231 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0026 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01168 | hp1 | a0001 | c0001 | t0030 | g0057 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0225 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01169 | hp2 | a0001 | c0001 | t0030 | g0056 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01175 | hp1 | a0002 | c0005 | t0046 | g0234 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01175 | hp2 | a0001 | c0001 | t0018 | g0088 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01192 | hp2 | a0001 | c0001 | t0062 | g0139 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0050 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01243 | hp2 | a0002 | c0004 | t0068 | g0173 | AMR | PUR | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01257 | hp1 | a0001 | c0001 | t0014 | g0133 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01257 | hp2 | a0001 | c0001 | t0015 | g0175 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01261 | hp2 | a0002 | c0002 | t0039 | g0232 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0280 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01361 | hp1 | a0002 | c0005 | t0004 | g0236 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01361 | hp2 | a0001 | c0003 | t0003 | g0307 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0308 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01433 | hp2 | a0002 | c0002 | t0016 | g0186 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0323 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01496 | hp2 | a0002 | c0002 | t0016 | g0177 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01515 | hp1 | a0002 | c0005 | t0051 | g0240 | EUR | IBS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01515 | hp2 | a0001 | c0019 | t0001 | g0111 | EUR | IBS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01516 | hp1 | a0002 | c0005 | t0004 | g0279 | EUR | IBS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01516 | hp2 | a0002 | c0009 | t0001 | g0284 | EUR | IBS | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01884 | hp1 | a0002 | c0002 | t0012 | g0210 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01884 | hp2 | a0004 | c0007 | t0034 | g0336 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01891 | hp1 | a0002 | c0010 | t0017 | g0170 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01891 | hp2 | a0002 | c0002 | t0021 | g0181 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01934 | hp1 | a0002 | c0005 | t0009 | g0241 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0318 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01943 | hp2 | a0001 | c0001 | t0015 | g0145 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0120 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0311 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0086 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0267 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01978 | hp1 | a0001 | c0003 | t0003 | g0322 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0328 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01981 | hp2 | a0014 | c0023 | t0002 | g0345 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01993 | hp1 | a0002 | c0004 | t0005 | g0006 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0272 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0324 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02004 | hp2 | a0001 | c0001 | t0018 | g0142 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02015 | hp2 | a0001 | c0003 | t0025 | g0301 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02027 | hp2 | a0002 | c0002 | t0010 | g0017 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02040 | hp2 | a0011 | c0017 | t0001 | g0104 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02055 | hp1 | a0001 | c0001 | t0029 | g0051 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02055 | hp2 | a0002 | c0009 | t0070 | g0033 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0275 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0128 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02080 | hp2 | a0002 | c0011 | t0037 | g0268 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02083 | hp1 | a0002 | c0004 | t0004 | g0278 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02083 | hp2 | a0001 | c0001 | t0031 | g0342 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02129 | hp1 | a0001 | c0003 | t0003 | g0317 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02129 | hp2 | a0002 | c0004 | t0005 | g0005 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02135 | hp1 | a0001 | c0003 | t0003 | g0288 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02135 | hp2 | a0002 | c0009 | t0001 | g0055 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02145 | hp1 | a0001 | c0001 | t0033 | g0164 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02145 | hp2 | a0002 | c0004 | t0005 | g0168 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02148 | hp1 | a0001 | c0003 | t0003 | g0306 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02148 | hp2 | a0001 | c0001 | t0071 | g0099 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | CDX | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02155 | hp2 | a0002 | c0002 | t0023 | g0264 | EAS | CDX | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02257 | hp1 | a0002 | c0004 | t0003 | g0194 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02257 | hp2 | a0003 | c0006 | t0001 | g0028 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02258 | hp1 | a0002 | c0004 | t0020 | g0191 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02258 | hp2 | a0002 | c0002 | t0012 | g0214 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02273 | hp1 | a0001 | c0003 | t0003 | g0327 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02273 | hp2 | a0001 | c0003 | t0003 | g0313 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02280 | hp1 | a0002 | c0002 | t0012 | g0212 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02280 | hp2 | a0002 | c0002 | t0026 | g0187 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02300 | hp1 | a0002 | c0004 | t0005 | g0011 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0245 | AMR | PEL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02451 | hp1 | a0001 | c0001 | t0058 | g0348 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | KHV | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02615 | hp1 | a0002 | c0010 | t0017 | g0172 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0330 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02622 | hp2 | a0002 | c0027 | t0003 | g0038 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02630 | hp2 | a0008 | c0020 | t0019 | g0341 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02647 | hp1 | a0002 | c0024 | t0002 | g0332 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02647 | hp2 | a0002 | c0010 | t0017 | g0169 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02698 | hp2 | a0002 | c0002 | t0035 | g0271 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02717 | hp1 | a0004 | c0007 | t0076 | g0337 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02717 | hp2 | a0003 | c0018 | t0061 | g0179 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0036 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02723 | hp2 | a0003 | c0006 | t0001 | g0027 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02735 | hp1 | a0002 | c0002 | t0016 | g0273 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0346 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02738 | hp1 | a0002 | c0005 | t0009 | g0235 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02809 | hp1 | a0002 | c0004 | t0005 | g0046 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02809 | hp2 | a0002 | c0002 | t0026 | g0202 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02895 | hp1 | a0005 | c0012 | t0074 | g0159 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02895 | hp2 | a0002 | c0002 | t0027 | g0013 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02896 | hp1 | a0002 | c0002 | t0005 | g0039 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02896 | hp2 | a0001 | c0008 | t0056 | g0217 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02897 | hp1 | a0002 | c0002 | t0005 | g0041 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02897 | hp2 | a0002 | c0002 | t0027 | g0012 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02922 | hp1 | a0004 | c0007 | t0034 | g0335 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02922 | hp2 | a0005 | c0012 | t0073 | g0160 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02965 | hp1 | a0003 | c0006 | t0015 | g0065 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0059 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02976 | hp2 | a0002 | c0004 | t0003 | g0244 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03041 | hp2 | a0003 | c0006 | t0001 | g0031 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03139 | hp1 | a0003 | c0006 | t0001 | g0029 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0054 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03209 | hp1 | a0002 | c0002 | t0012 | g0211 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03209 | hp2 | a0002 | c0004 | t0003 | g0204 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0035 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03225 | hp2 | a0003 | c0006 | t0001 | g0030 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03239 | hp2 | a0002 | c0002 | t0035 | g0276 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03453 | hp1 | a0002 | c0009 | t0011 | g0053 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03486 | hp1 | a0002 | c0004 | t0066 | g0045 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03486 | hp2 | a0002 | c0026 | t0003 | g0201 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0229 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03490 | hp2 | a0001 | c0001 | t0022 | g0074 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03491 | hp1 | a0001 | c0001 | t0015 | g0143 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03491 | hp2 | a0002 | c0005 | t0004 | g0233 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0331 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03516 | hp2 | a0003 | c0006 | t0001 | g0032 | AFR | ESN | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03540 | hp1 | a0002 | c0004 | t0024 | g0184 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03540 | hp2 | a0002 | c0002 | t0012 | g0213 | AFR | GWD | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03579 | hp1 | a0013 | c0021 | t0077 | g0010 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0333 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03669 | hp2 | a0002 | c0004 | t0049 | g0196 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03688 | hp1 | a0002 | c0004 | t0003 | g0219 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03688 | hp2 | a0002 | c0002 | t0041 | g0266 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03704 | hp1 | a0002 | c0002 | t0042 | g0018 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03710 | hp2 | a0001 | c0001 | t0022 | g0085 | SAS | PJL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03831 | hp1 | a0001 | c0001 | t0022 | g0161 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0148 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03834 | hp1 | a0002 | c0004 | t0005 | g0007 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03927 | hp1 | a0001 | c0003 | t0052 | g0292 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0309 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03942 | hp1 | a0001 | c0001 | t0032 | g0091 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03942 | hp2 | a0001 | c0001 | t0059 | g0064 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG04184 | hp2 | a0001 | c0001 | t0014 | g0067 | SAS | BEB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG04199 | hp2 | a0002 | c0004 | t0003 | g0183 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG04204 | hp1 | a0002 | c0004 | t0003 | g0176 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG04228 | hp1 | a0002 | c0004 | t0003 | g0218 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0263 | SAS | STU | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0052 | AFR | YRI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18522 | hp2 | a0001 | c0001 | t0033 | g0163 | AFR | YRI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18612 | hp1 | a0002 | c0002 | t0010 | g0022 | EAS | CHB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18612 | hp2 | a0002 | c0004 | t0005 | g0008 | EAS | CHB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18747 | hp1 | a0001 | c0001 | t0031 | g0343 | EAS | CHB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18747 | hp2 | a0002 | c0002 | t0010 | g0024 | EAS | CHB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0329 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18941 | hp1 | a0002 | c0002 | t0010 | g0020 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18941 | hp2 | a0001 | c0001 | t0032 | g0105 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18942 | hp2 | a0002 | c0004 | t0004 | g0207 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18943 | hp1 | a0002 | c0002 | t0040 | g0230 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18944 | hp2 | a0001 | c0003 | t0004 | g0291 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0286 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18950 | hp1 | a0001 | c0003 | t0003 | g0326 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18951 | hp2 | a0001 | c0001 | t0060 | g0069 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18953 | hp2 | a0002 | c0004 | t0054 | g0190 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18956 | hp1 | a0001 | c0003 | t0003 | g0296 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18961 | hp1 | a0010 | c0016 | t0003 | g0289 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18964 | hp1 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18964 | hp2 | a0001 | c0001 | t0014 | g0127 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18967 | hp1 | a0002 | c0004 | t0053 | g0216 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18967 | hp2 | a0001 | c0001 | t0014 | g0153 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18969 | hp2 | a0002 | c0004 | t0005 | g0015 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18971 | hp2 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18972 | hp1 | a0002 | c0004 | t0004 | g0206 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18973 | hp2 | a0002 | c0004 | t0004 | g0208 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18974 | hp2 | a0006 | c0025 | t0025 | g0293 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18979 | hp1 | a0002 | c0004 | t0004 | g0195 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18981 | hp2 | a0002 | c0002 | t0055 | g0304 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18982 | hp2 | a0001 | c0001 | t0044 | g0048 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18983 | hp1 | a0002 | c0011 | t0002 | g0260 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0297 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18989 | hp1 | a0002 | c0004 | t0004 | g0209 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18991 | hp2 | a0002 | c0004 | t0004 | g0189 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18993 | hp1 | a0001 | c0001 | t0043 | g0047 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18993 | hp2 | a0001 | c0003 | t0020 | g0325 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18994 | hp1 | a0002 | c0004 | t0004 | g0215 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18994 | hp2 | a0001 | c0003 | t0007 | g0066 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0125 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19001 | hp1 | a0001 | c0001 | t0015 | g0117 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0334 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0300 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19005 | hp2 | a0001 | c0003 | t0003 | g0298 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19007 | hp1 | a0002 | c0002 | t0010 | g0023 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19012 | hp1 | a0001 | c0001 | t0064 | g0146 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19043 | hp1 | a0002 | c0010 | t0017 | g0171 | AFR | LWK | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0305 | AFR | LWK | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0287 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19060 | hp1 | a0001 | c0001 | t0007 | g0285 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19060 | hp2 | a0012 | c0022 | t0023 | g0265 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19062 | hp1 | a0001 | c0001 | t0065 | g0095 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19062 | hp2 | a0002 | c0002 | t0010 | g0021 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19066 | hp1 | a0002 | c0004 | t0067 | g0009 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19066 | hp2 | a0002 | c0004 | t0021 | g0180 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19067 | hp1 | a0002 | c0004 | t0004 | g0205 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0108 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19068 | hp2 | a0001 | c0003 | t0003 | g0303 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19083 | hp1 | a0001 | c0003 | t0003 | g0315 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19083 | hp2 | a0002 | c0004 | t0057 | g0220 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19086 | hp1 | a0009 | c0015 | t0003 | g0096 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0350 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19087 | hp1 | a0001 | c0003 | t0047 | g0294 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19240 | hp1 | a0002 | c0004 | t0005 | g0043 | AFR | YRI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA19240 | hp2 | a0002 | c0002 | t0005 | g0025 | AFR | YRI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0283 | AFR | ASW | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA20129 | hp2 | a0001 | c0008 | t0028 | g0016 | AFR | ASW | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA20752 | hp1 | a0001 | c0003 | t0003 | g0319 | EUR | TSI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01123 | hp1 | a0001 | c0003 | t0003 | g0316 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02109 | hp1 | a0002 | c0002 | t0045 | g0203 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02109 | hp2 | a0002 | c0004 | t0005 | g0042 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0349 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0062 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02559 | hp1 | a0001 | c0001 | t0029 | g0347 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG02559 | hp2 | a0004 | c0007 | t0075 | g0338 | AFR | ACB | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03471 | hp1 | a0002 | c0004 | t0003 | g0193 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG03471 | hp2 | a0001 | c0008 | t0028 | g0014 | AFR | MSL | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG06807 | hp1 | a0007 | c0014 | t0019 | g0340 | AFR | USA | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| HG06807 | hp2 | a0002 | c0004 | t0069 | g0040 | AFR | USA | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA18955 | hp2 | a0001 | c0001 | t0014 | g0094 | EAS | JPT | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA20300 | hp1 | a0001 | c0003 | t0020 | g0004 | AFR | USA | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA20300 | hp2 | a0002 | c0004 | t0024 | g0185 | AFR | USA | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA21309 | hp1 | a0002 | c0004 | t0021 | g0182 | AFR | LWK | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| NA21309 | hp2 | a0002 | c0004 | t0005 | g0044 | AFR | LWK | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0005 | t0009 | g0237 | REF | REF | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0063 | g0192 | REF | REF | MLXIP_chr12_122073756_122152344 | MLXIP | chr12 | 122073756 | 122152344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122078986
|
G | A | 1 | a0015 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.133G>A | p.Gly45Ser | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 231/8390 | 133/2760 | 45/919 | chr12 | 122078986 | ||
| chr12:122127352
|
G | T | 1 | a0006 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.510G>T | p.Trp170Cys | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/17 | 608/8390 | 510/2760 | 170/919 | chr12 | 122127352 | ||
| chr12:122133372
|
C | A | 3 | a0004a0005a0007 | 8 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(5): Show |
missense_variant | MODERATE | c.1117C>A | p.Leu373Ile | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1215/8390 | 1117/2760 | 373/919 | chr12 | 122133372 | ||
| chr12:122133442
|
A | G | 6 | a0002a0007a0012others(3): Show | 150 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(147): Show |
missense_variant | MODERATE | c.1187A>G | p.Glu396Gly | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1285/8390 | 1187/2760 | 396/919 | chr12 | 122133442 | ||
| chr12:122133697
|
C | T | 4 | a0004a0005a0007others(1): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
missense_variant | MODERATE | c.1442C>T | p.Pro481Leu | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1540/8390 | 1442/2760 | 481/919 | chr12 | 122133697 | ||
| chr12:122133870
|
G | T | 1 | a0003 | 8 | HG02257.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.1615G>T | p.Val539Leu | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1713/8390 | 1615/2760 | 539/919 | chr12 | 122133870 | ||
| chr12:122133915
|
C | G | 1 | a0009 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.1660C>G | p.Pro554Ala | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1758/8390 | 1660/2760 | 554/919 | chr12 | 122133915 | ||
| chr12:122135301
|
G | A | 1 | a0010 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.1810G>A | p.Val604Met | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 10/17 | 1908/8390 | 1810/2760 | 604/919 | chr12 | 122135301 | ||
| chr12:122138248
|
A | G | 1 | a0014 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.2209A>G | p.Met737Val | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 13/17 | 2307/8390 | 2209/2760 | 737/919 | chr12 | 122138248 | ||
| chr12:122138529
|
G | A | 1 | a0011 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2362G>A | p.Glu788Lys | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 14/17 | 2460/8390 | 2362/2760 | 788/919 | chr12 | 122138529 | ||
| chr12:122138895
|
AATACGTG others(8): Show |
A | 1 | a0012 | 1 | NA19060.hp2 | disruptive_inframe_deletion | MODERATE | c.2466_2480delATACGT others(9): Show |
p.Tyr823_Arg827del | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/17 | 2564/8390 | 2466/2760 | 822/919 | chr12 | 122138895 | ||
| chr12:122140961
|
T | G | 1 | a0005 | 2 | HG02895.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.2516T>G | p.Ile839Ser | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/17 | 2614/8390 | 2516/2760 | 839/919 | chr12 | 122140961 | ||
| chr12:122141784
|
G | A | 1 | a0013 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.2732G>A | p.Arg911Lys | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2830/8390 | 2732/2760 | 911/919 | chr12 | 122141784 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122078886
|
C | T | 2 | a0002c0026a0002c0027 | 2 | HG02622.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.33C>T | p.Arg11Arg | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 131/8390 | 33/2760 | 11/919 | chr12 | 122078886 | ||
| chr12:122078895
|
C | T | 1 | a0002c0011 | 3 | HG00558.hp2 HG02080.hp2 NA18983.hp1 |
synonymous_variant | LOW | c.42C>T | p.Arg14Arg | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 140/8390 | 42/2760 | 14/919 | chr12 | 122078895 | ||
| chr12:122078991
|
G | A | 1 | a0002c0005 | 12 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(9): Show |
synonymous_variant | LOW | c.138G>A | p.Ala46Ala | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 236/8390 | 138/2760 | 46/919 | chr12 | 122078991 | ||
| chr12:122133584
|
A | G | 7 | a0001c0008a0002c0002a0002c0011others(4): Show | 89 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(86): Show |
synonymous_variant | LOW | c.1329A>G | p.Pro443Pro | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1427/8390 | 1329/2760 | 443/919 | chr12 | 122133584 | ||
| chr12:122133743
|
C | T | 1 | a0002c0010 | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
synonymous_variant | LOW | c.1488C>T | p.Ala496Ala | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1586/8390 | 1488/2760 | 496/919 | chr12 | 122133743 | ||
| chr12:122133746
|
C | T | 1 | a0001c0019 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.1491C>T | p.Pro497Pro | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1589/8390 | 1491/2760 | 497/919 | chr12 | 122133746 | ||
| chr12:122133887
|
A | G | 1 | a0002c0027 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1632A>G | p.Val544Val | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1730/8390 | 1632/2760 | 544/919 | chr12 | 122133887 | ||
| chr12:122133914
|
G | A | 1 | a0009c0015 | 1 | NA19086.hp1 | synonymous_variant | LOW | c.1659G>A | p.Gln553Gln | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/17 | 1757/8390 | 1659/2760 | 553/919 | chr12 | 122133914 | ||
| chr12:122135327
|
G | T | 1 | a0002c0024 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1836G>T | p.Ala612Ala | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 10/17 | 1934/8390 | 1836/2760 | 612/919 | chr12 | 122135327 | ||
| chr12:122138453
|
T | C | 22 | a0001c0003a0001c0008a0002c0002others(19): Show | 205 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
synonymous_variant | LOW | c.2286T>C | p.Thr762Thr | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 14/17 | 2384/8390 | 2286/2760 | 762/919 | chr12 | 122138453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122078765
|
GCGGGC | G | 3 | a0004c0007t0019a0007c0014t0019a0008c0020t0019 | 3 | HG01099.hp2 HG02630.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75_-71delGCCGG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 71 | INFO_REALIGN_3_PRIME | chr12 | 122078765 | ||||
| chr12:122078767
|
G | T | 1 | a0002c0002t0035 | 2 | HG02698.hp2 HG03239.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | chr12 | 122078767 | ||||||
| chr12:122078770
|
C | T | 1 | a0001c0001t0078 | 1 | HG00609.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 84 | chr12 | 122078770 | |||||
| chr12:122078773
|
G | T | 1 | a0013c0021t0077 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 81 | chr12 | 122078773 | |||||
| chr12:122078797
|
C | T | 8 | a0004c0007t0019a0004c0007t0034a0004c0007t0075others(5): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | chr12 | 122078797 | ||||||
| chr12:122078801
|
C | T | 1 | a0002c0002t0072 | 1 | HG00621.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 53 | chr12 | 122078801 | |||||
| chr12:122078811
|
G | A | 1 | a0001c0001t0036 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/17 | 43 | chr12 | 122078811 | |||||
| chr12:122141831
|
G | A | 1 | a0002c0011t0037 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*19G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 19 | chr12 | 122141831 | |||||
| chr12:122141834
|
G | A | 15 | a0002c0002t0002a0002c0002t0016a0002c0002t0023others(12): Show | 62 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*22G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 22 | chr12 | 122141834 | |||||
| chr12:122141938
|
A | G | 1 | a0001c0001t0033 | 2 | HG02145.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*126A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 126 | chr12 | 122141938 | |||||
| chr12:122142054
|
C | G | 6 | a0004c0007t0019a0004c0007t0034a0004c0007t0075others(3): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*242C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 242 | chr12 | 122142054 | |||||
| chr12:122142153
|
G | A | 3 | a0001c0001t0043a0001c0001t0044a0002c0002t0042 | 3 | HG03704.hp1 NA18982.hp2 NA18993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*341G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 341 | chr12 | 122142153 | |||||
| chr12:122142153
|
G | C | 1 | a0002c0002t0045 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 341 | chr12 | 122142153 | |||||
| chr12:122142159
|
G | A | 1 | a0013c0021t0077 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 347 | chr12 | 122142159 | |||||
| chr12:122142209
|
CCCTCCTG others(3): Show |
C | 1 | a0013c0021t0077 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*399_*408delCTCCTG others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 399 | INFO_REALIGN_3_PRIME | chr12 | 122142209 | ||||
| chr12:122142262
|
C | T | 1 | a0001c0001t0071 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*450C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 450 | chr12 | 122142262 | |||||
| chr12:122142295
|
G | A | 53 | a0001c0003t0003a0001c0003t0004a0001c0003t0020others(50): Show | 175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*483G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 483 | chr12 | 122142295 | |||||
| chr12:122142616
|
C | T | 2 | a0001c0008t0028a0002c0002t0027 | 4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*804C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 804 | chr12 | 122142616 | |||||
| chr12:122142617
|
G | A | 1 | a0002c0002t0038 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 805 | chr12 | 122142617 | |||||
| chr12:122142824
|
G | A | 26 | a0001c0003t0003a0001c0003t0004a0001c0003t0020others(23): Show | 86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1012G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1012 | chr12 | 122142824 | |||||
| chr12:122142868
|
G | C | 4 | a0001c0001t0011a0001c0001t0029a0001c0001t0030others(1): Show | 10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1056G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1056 | chr12 | 122142868 | |||||
| chr12:122143135
|
C | T | 1 | a0002c0010t0017 | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1323C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1323 | chr12 | 122143135 | |||||
| chr12:122143339
|
C | T | 6 | a0001c0008t0028a0002c0002t0010a0002c0002t0027others(3): Show | 13 | HG00621.hp2 HG02027.hp2 HG02895.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1527C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1527 | chr12 | 122143339 | |||||
| chr12:122143672
|
T | C | 54 | a0001c0003t0003a0001c0003t0004a0001c0003t0020others(51): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1860T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1860 | chr12 | 122143672 | |||||
| chr12:122143754
|
C | T | 1 | a0013c0021t0077 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1942C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1942 | chr12 | 122143754 | |||||
| chr12:122143760
|
G | T | 1 | a0002c0009t0070 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1948G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1948 | chr12 | 122143760 | |||||
| chr12:122143788
|
G | C | 2 | a0001c0001t0013a0001c0001t0058 | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1976G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 1976 | chr12 | 122143788 | |||||
| chr12:122143822
|
C | G | 1 | a0001c0001t0030 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2010C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2010 | chr12 | 122143822 | |||||
| chr12:122143882
|
T | A | 16 | a0002c0002t0002a0002c0002t0016a0002c0002t0023others(13): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2070T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2070 | chr12 | 122143882 | |||||
| chr12:122143918
|
G | A | 2 | a0002c0002t0023a0012c0022t0023 | 2 | HG02155.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2106G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2106 | chr12 | 122143918 | |||||
| chr12:122143969
|
A | T | 54 | a0001c0003t0003a0001c0003t0004a0001c0003t0020others(51): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2157A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2157 | chr12 | 122143969 | |||||
| chr12:122143990
|
C | T | 16 | a0001c0001t0013a0001c0001t0058a0002c0002t0005others(13): Show | 33 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2178C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2178 | chr12 | 122143990 | |||||
| chr12:122144202
|
G | T | 2 | a0001c0001t0013a0001c0001t0058 | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2390G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2390 | chr12 | 122144202 | |||||
| chr12:122144203
|
G | T | 2 | a0001c0001t0013a0001c0001t0058 | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2391G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2391 | chr12 | 122144203 | |||||
| chr12:122144215
|
C | T | 1 | a0002c0004t0054 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2403 | chr12 | 122144215 | |||||
| chr12:122144418
|
C | CA | 14 | a0001c0001t0007a0001c0001t0014a0001c0001t0029others(11): Show | 35 | HG01106.hp2 HG01175.hp1 HG01257.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2630dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2631 | INFO_REALIGN_3_PRIME | chr12 | 122144418 | ||||
| chr12:122144418
|
CA | C | 6 | a0001c0001t0015a0001c0001t0065a0001c0003t0025others(3): Show | 9 | HG01257.hp2 HG01943.hp2 HG02015.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2630delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2630 | INFO_REALIGN_3_PRIME | chr12 | 122144418 | ||||
| chr12:122144418
|
CAAAAAA | C | 2 | a0001c0008t0056a0002c0002t0012 | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2625_*2630delAAAA others(2): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2625 | INFO_REALIGN_3_PRIME | chr12 | 122144418 | ||||
| chr12:122144418
|
CAAAAAAA others(3): Show |
C | 18 | a0002c0002t0002a0002c0002t0016a0002c0002t0023others(15): Show | 69 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2621_*2630delAAAA others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2621 | INFO_REALIGN_3_PRIME | chr12 | 122144418 | ||||
| chr12:122144454
|
G | A | 2 | a0001c0008t0056a0002c0002t0012 | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2642G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2642 | chr12 | 122144454 | |||||
| chr12:122144662
|
G | A | 2 | a0001c0001t0033a0002c0009t0070 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2850G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2850 | chr12 | 122144662 | |||||
| chr12:122144737
|
A | G | 1 | a0002c0002t0041 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2925A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 2925 | chr12 | 122144737 | |||||
| chr12:122144865
|
T | C | 1 | a0002c0004t0066 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3053T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3053 | chr12 | 122144865 | |||||
| chr12:122144914
|
A | G | 1 | a0001c0001t0064 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3102A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3102 | chr12 | 122144914 | |||||
| chr12:122145069
|
T | C | 1 | a0001c0001t0031 | 2 | HG02083.hp2 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3257T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3257 | chr12 | 122145069 | |||||
| chr12:122145260
|
G | A | 1 | a0002c0002t0039 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3448G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3448 | chr12 | 122145260 | |||||
| chr12:122145317
|
A | G | 59 | a0001c0003t0003a0001c0003t0004a0001c0003t0020others(56): Show | 193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*3505A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3505 | chr12 | 122145317 | |||||
| chr12:122145323
|
C | T | 3 | a0005c0012t0073a0005c0012t0074a0013c0021t0077 | 3 | HG02895.hp1 HG02922.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3511C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3511 | chr12 | 122145323 | |||||
| chr12:122145328
|
A | G | 32 | a0001c0003t0003a0001c0003t0004a0001c0003t0020others(29): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*3516A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3516 | chr12 | 122145328 | |||||
| chr12:122145462
|
G | T | 63 | a0001c0003t0003a0001c0003t0004a0001c0003t0020others(60): Show | 193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*3650G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3650 | chr12 | 122145462 | |||||
| chr12:122145738
|
G | A | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(30): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*3926G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3926 | chr12 | 122145738 | |||||
| chr12:122145769
|
G | C | 1 | a0004c0007t0075 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3957G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3957 | chr12 | 122145769 | |||||
| chr12:122145786
|
G | A | 8 | a0004c0007t0019a0004c0007t0034a0004c0007t0075others(5): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3974G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3974 | chr12 | 122145786 | |||||
| chr12:122145803
|
C | T | 1 | a0002c0004t0053 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3991C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 3991 | chr12 | 122145803 | |||||
| chr12:122145855
|
C | T | 1 | a0013c0021t0077 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4043C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4043 | chr12 | 122145855 | |||||
| chr12:122145928
|
C | T | 1 | a0001c0001t0044 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4116C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4116 | chr12 | 122145928 | |||||
| chr12:122145947
|
G | A | 1 | a0001c0001t0058 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4135G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4135 | chr12 | 122145947 | |||||
| chr12:122146106
|
G | C | 1 | a0002c0005t0009 | 6 | HG00323.hp1 HG01099.hp1 HG01109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4294G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4294 | chr12 | 122146106 | |||||
| chr12:122146146
|
T | C | 6 | a0004c0007t0019a0004c0007t0034a0004c0007t0075others(3): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4334T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4334 | chr12 | 122146146 | |||||
| chr12:122146181
|
G | A | 1 | a0001c0008t0048 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4369G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4369 | chr12 | 122146181 | |||||
| chr12:122146362
|
G | A | 58 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(55): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*4550G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4550 | chr12 | 122146362 | |||||
| chr12:122146368
|
C | T | 57 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(54): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*4556C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4556 | chr12 | 122146368 | |||||
| chr12:122146371
|
A | G | 1 | a0001c0003t0047 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4559A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4559 | chr12 | 122146371 | |||||
| chr12:122146408
|
C | T | 1 | a0002c0004t0024 | 2 | HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4596C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4596 | chr12 | 122146408 | |||||
| chr12:122146414
|
C | T | 1 | a0002c0010t0017 | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4602C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4602 | chr12 | 122146414 | |||||
| chr12:122146439
|
C | T | 1 | a0001c0008t0028 | 2 | HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4627C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4627 | chr12 | 122146439 | |||||
| chr12:122146559
|
A | G | 7 | a0002c0002t0005a0002c0002t0012a0002c0004t0005others(4): Show | 23 | HG01243.hp2 HG01884.hp1 HG01993.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4747A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4747 | chr12 | 122146559 | |||||
| chr12:122146574
|
G | A | 1 | a0002c0004t0049 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4762G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4762 | chr12 | 122146574 | |||||
| chr12:122146621
|
CGT | C | 38 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(35): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*4827_*4828delTG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4827 | INFO_REALIGN_3_PRIME | chr12 | 122146621 | ||||
| chr12:122146621
|
CGTGT | C | 2 | a0001c0001t0022a0001c0001t0059 | 4 | HG03490.hp2 HG03710.hp2 HG03831.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4825_*4828delTGTG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4825 | INFO_REALIGN_3_PRIME | chr12 | 122146621 | ||||
| chr12:122146641
|
C | T | 1 | a0002c0004t0024 | 2 | HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4829C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4829 | chr12 | 122146641 | |||||
| chr12:122146642
|
A | G | 1 | a0002c0004t0024 | 2 | HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4830A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4830 | chr12 | 122146642 | |||||
| chr12:122146642
|
ACG | A | 23 | a0001c0001t0062a0001c0003t0003a0001c0003t0004others(20): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*4837_*4838delCG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4837 | INFO_REALIGN_3_PRIME | chr12 | 122146642 | ||||
| chr12:122146644
|
G | A | 1 | a0002c0004t0024 | 2 | HG03540.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4832G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4832 | chr12 | 122146644 | |||||
| chr12:122146646
|
G | A | 5 | a0002c0002t0005a0002c0004t0005a0002c0004t0066others(2): Show | 17 | HG01993.hp1 HG02109.hp2 HG02129.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4834G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4834 | chr12 | 122146646 | |||||
| chr12:122146661
|
G | T | 68 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(65): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*4849G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4849 | chr12 | 122146661 | |||||
| chr12:122146701
|
G | A | 1 | a0001c0008t0028 | 2 | HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4889G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4889 | chr12 | 122146701 | |||||
| chr12:122146737
|
TGGTTCTG others(15): Show |
T | 6 | a0002c0002t0005a0002c0004t0005a0002c0004t0066others(3): Show | 18 | HG01243.hp2 HG01993.hp1 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4926_*4947delGGTT others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4926 | chr12 | 122146737 | |||||
| chr12:122146791
|
T | C | 2 | a0001c0001t0044a0001c0008t0048 | 2 | HG00597.hp2 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4979T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 4979 | chr12 | 122146791 | |||||
| chr12:122146934
|
C | T | 11 | a0001c0003t0004a0001c0008t0028a0001c0008t0056others(8): Show | 28 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5122C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5122 | chr12 | 122146934 | |||||
| chr12:122146938
|
T | G | 6 | a0002c0002t0005a0002c0004t0005a0002c0004t0066others(3): Show | 18 | HG01243.hp2 HG01993.hp1 HG02109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5126T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5126 | chr12 | 122146938 | |||||
| chr12:122146945
|
T | C | 1 | a0013c0021t0077 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5133T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5133 | chr12 | 122146945 | |||||
| chr12:122146980
|
T | G | 1 | a0001c0003t0050 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5168T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5168 | chr12 | 122146980 | |||||
| chr12:122147006
|
G | A | 1 | a0001c0001t0060 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5194G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5194 | chr12 | 122147006 | |||||
| chr12:122147046
|
T | C | 2 | a0001c0001t0013a0001c0001t0058 | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5234T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5234 | chr12 | 122147046 | |||||
| chr12:122147131
|
G | C | 1 | a0013c0021t0077 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5319G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5319 | chr12 | 122147131 | |||||
| chr12:122147205
|
T | C | 53 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(50): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*5393T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5393 | chr12 | 122147205 | |||||
| chr12:122147255
|
C | T | 12 | a0002c0002t0005a0002c0004t0005a0002c0004t0066others(9): Show | 25 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5443C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5443 | chr12 | 122147255 | |||||
| chr12:122147298
|
C | G | 13 | a0002c0002t0005a0002c0004t0005a0002c0004t0066others(10): Show | 26 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5486C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 17/17 | 5486 | chr12 | 122147298 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122079288
|
T | C | 20 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(17): Show | 20 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+22T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079288 | ||||||
| chr12:122079309
|
T | C | 1 | a0002c0002t0005g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.413+43T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079309 | ||||||
| chr12:122079331
|
A | G | 1 | a0002c0002t0002g0350 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+65A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079331 | ||||||
| chr12:122079450
|
T | A | 1 | a0002c0002t0002g0350 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+184T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079450 | ||||||
| chr12:122079489
|
T | A | 1 | a0001c0001t0008g0026 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.413+223T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079489 | ||||||
| chr12:122079567
|
T | A | 1 | a0002c0002t0002g0350 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+301T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079567 | ||||||
| chr12:122079858
|
T | C | 6 | a0003c0006t0001g0027a0003c0006t0001g0028a0003c0006t0001g0029others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+592T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079858 | ||||||
| chr12:122079937
|
A | C | 3 | a0001c0001t0013g0349a0001c0001t0029g0347a0001c0001t0058g0348 | 3 | HG02451.hp1 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+671A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122079937 | ||||||
| chr12:122080041
|
T | C | 1 | a0002c0009t0070g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+775T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080041 | ||||||
| chr12:122080123
|
C | T | 1 | a0001c0001t0007g0346 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.413+857C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080123 | ||||||
| chr12:122080155
|
T | C | 4 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(1): Show | 4 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+889T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080155 | ||||||
| chr12:122080337
|
A | G | 2 | a0002c0002t0002g0344a0014c0023t0002g0345 | 2 | HG00323.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.413+1071A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080337 | ||||||
| chr12:122080345
|
A | G | 2 | a0001c0001t0031g0342a0001c0001t0031g0343 | 2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.413+1079A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080345 | ||||||
| chr12:122080482
|
A | T | 7 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+1216A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080482 | ||||||
| chr12:122080505
|
C | T | 20 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(17): Show | 20 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+1239C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080505 | ||||||
| chr12:122080733
|
G | T | 1 | a0001c0001t0006g0334 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.413+1467G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080733 | ||||||
| chr12:122080953
|
G | A | 1 | a0002c0027t0003g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.413+1687G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122080953 | ||||||
| chr12:122081029
|
CT | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.413+1765delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122081029 | |||||
| chr12:122081053
|
A | G | 1 | a0002c0004t0005g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.413+1787A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081053 | ||||||
| chr12:122081119
|
C | G | 4 | a0002c0002t0002g0330a0002c0002t0002g0331a0002c0002t0002g0333others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+1853C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081119 | ||||||
| chr12:122081182
|
G | A | 10 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+1916G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081182 | ||||||
| chr12:122081287
|
G | A | 10 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+2021G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081287 | ||||||
| chr12:122081427
|
G | C | 3 | a0001c0001t0001g0049a0001c0001t0043g0047a0001c0001t0044g0048 | 3 | NA18982.hp2 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.413+2161G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081427 | ||||||
| chr12:122081564
|
T | C | 4 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(1): Show | 4 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+2298T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081564 | ||||||
| chr12:122081755
|
A | T | 3 | a0001c0001t0013g0349a0001c0001t0029g0347a0001c0001t0058g0348 | 3 | HG02451.hp1 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+2489A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081755 | ||||||
| chr12:122081887
|
C | T | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+2621C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081887 | ||||||
| chr12:122081945
|
T | G | 4 | a0004c0007t0034g0335a0004c0007t0034g0336a0004c0007t0075g0338others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+2679T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122081945 | ||||||
| chr12:122082179
|
G | T | 3 | a0001c0001t0008g0165a0001c0001t0008g0166a0001c0001t0008g0167 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.413+2913G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082179 | ||||||
| chr12:122082206
|
C | T | 47 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.413+2940C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082206 | ||||||
| chr12:122082244
|
G | C | 1 | a0002c0002t0002g0350 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+2978G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082244 | ||||||
| chr12:122082245
|
C | G | 1 | a0002c0002t0002g0350 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413+2979C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082245 | ||||||
| chr12:122082287
|
C | T | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+3021C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082287 | ||||||
| chr12:122082669
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.413+3403A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082669 | ||||||
| chr12:122082672
|
T | C | 3 | a0001c0001t0013g0349a0001c0001t0029g0347a0001c0001t0058g0348 | 3 | HG02451.hp1 HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+3406T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082672 | ||||||
| chr12:122082967
|
C | T | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+3701C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122082967 | ||||||
| chr12:122083076
|
T | C | 20 | a0001c0003t0003g0286a0001c0003t0003g0287a0001c0003t0003g0288others(17): Show | 20 | HG00597.hp2 HG00673.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+3810T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083076 | ||||||
| chr12:122083461
|
C | G | 2 | a0001c0001t0033g0163a0001c0001t0033g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+4195C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083461 | ||||||
| chr12:122083542
|
G | A | 4 | a0002c0010t0017g0169a0002c0010t0017g0170a0002c0010t0017g0171others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+4276G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083542 | ||||||
| chr12:122083571
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.413+4305T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083571 | ||||||
| chr12:122083580
|
A | G | 4 | a0002c0002t0002g0280a0002c0002t0002g0281a0002c0002t0002g0282others(1): Show | 4 | HG01358.hp2 NA18947.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4314A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083580 | ||||||
| chr12:122083643
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.413+4377A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083643 | ||||||
| chr12:122083710
|
G | T | 11 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+4444G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122083710 | ||||||
| chr12:122084056
|
G | A | 9 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(6): Show | 9 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+4790G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084056 | ||||||
| chr12:122084144
|
T | TTG | 20 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0178others(17): Show | 20 | HG01433.hp2 HG01891.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.413+4926_413+4927d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
T | TTGTG | 9 | a0001c0001t0001g0058a0001c0001t0001g0174a0001c0001t0007g0346others(6): Show | 9 | HG01168.hp1 HG01169.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+4924_413+4927d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
T | TTGTGTG | 4 | a0001c0001t0011g0052a0001c0001t0011g0054a0002c0004t0005g0005others(1): Show | 4 | HG02129.hp2 HG03195.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4922_413+4927d others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0029g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.413+4916_413+4927d others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0011g0050 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+4912_413+4927d others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
TTG | T | 87 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(84): Show | 87 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.413+4926_413+4927d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
TTGTG | T | 73 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0078others(70): Show | 73 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.413+4924_413+4927d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
TTGTGTG | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.413+4922_413+4927d others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
TTGTGTGT others(1): Show |
T | 16 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(13): Show | 16 | HG00280.hp1 HG00735.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+4920_413+4927d others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
TTGTGTGT others(3): Show |
T | 2 | a0002c0002t0005g0039a0002c0004t0069g0040 | 2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.413+4918_413+4927d others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
TTGTGTGT others(5): Show |
T | 4 | a0002c0002t0010g0017a0002c0002t0042g0018a0002c0004t0005g0043others(1): Show | 4 | HG02027.hp2 HG03704.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4916_413+4927d others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
TTGTGTGT others(7): Show |
T | 15 | a0001c0001t0022g0161a0001c0008t0028g0016a0002c0002t0005g0025others(12): Show | 15 | HG00621.hp2 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+4914_413+4927d others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084144
|
TTGTGTGT others(11): Show |
T | 1 | a0014c0023t0002g0345 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.413+4910_413+4927d others(20): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122084144 | |||||
| chr12:122084259
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.413+4993C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084259 | ||||||
| chr12:122084295
|
C | A | 1 | a0002c0009t0001g0055 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.413+5029C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084295 | ||||||
| chr12:122084462
|
G | A | 1 | a0002c0002t0039g0232 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.413+5196G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084462 | ||||||
| chr12:122084477
|
G | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0154others(4): Show | 7 | HG00280.hp1 HG00735.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+5211G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084477 | ||||||
| chr12:122084607
|
C | T | 1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+5341C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084607 | ||||||
| chr12:122084705
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.413+5439C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084705 | ||||||
| chr12:122084801
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.413+5535G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084801 | ||||||
| chr12:122084815
|
T | C | 11 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0001g0188others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+5549T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084815 | ||||||
| chr12:122084871
|
C | G | 10 | a0001c0003t0003g0306a0001c0003t0003g0307a0001c0003t0003g0322others(7): Show | 10 | HG01361.hp2 HG01496.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+5605C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084871 | ||||||
| chr12:122084960
|
C | T | 1 | a0002c0002t0035g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413+5694C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122084960 | ||||||
| chr12:122085014
|
T | C | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+5748T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085014 | ||||||
| chr12:122085015
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.413+5749T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085015 | ||||||
| chr12:122085028
|
G | C | 1 | a0002c0004t0003g0204 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.413+5762G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085028 | ||||||
| chr12:122085266
|
AC | A | 11 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+6002delC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122085266 | |||||
| chr12:122085405
|
A | AT | 7 | a0001c0001t0001g0152a0001c0001t0013g0349a0001c0001t0014g0153others(4): Show | 7 | HG02056.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+6155dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122085405 | |||||
| chr12:122085405
|
AT | A | 6 | a0001c0001t0014g0094a0001c0001t0030g0056a0001c0001t0033g0163others(3): Show | 6 | HG01099.hp2 HG01169.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+6155delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122085405 | |||||
| chr12:122085511
|
C | T | 1 | a0008c0020t0019g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.413+6245C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085511 | ||||||
| chr12:122085555
|
C | G | 1 | a0001c0008t0028g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413+6289C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085555 | ||||||
| chr12:122085762
|
T | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.413+6496T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085762 | ||||||
| chr12:122085778
|
A | G | 1 | a0001c0001t0032g0091 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.413+6512A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085778 | ||||||
| chr12:122085841
|
T | C | 5 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(2): Show | 5 | HG02723.hp1 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+6575T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085841 | ||||||
| chr12:122085846
|
A | G | 1 | a0002c0002t0002g0282 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.413+6580A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085846 | ||||||
| chr12:122085895
|
C | T | 2 | a0004c0007t0019g0339a0008c0020t0019g0341 | 2 | HG01099.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.413+6629C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085895 | ||||||
| chr12:122085944
|
C | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.413+6678C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085944 | ||||||
| chr12:122085982
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.413+6716G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122085982 | ||||||
| chr12:122086087
|
A | T | 1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6821A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086087 | ||||||
| chr12:122086088
|
A | T | 1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6822A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086088 | ||||||
| chr12:122086089
|
A | G | 1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6823A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086089 | ||||||
| chr12:122086095
|
G | A | 1 | a0002c0004t0020g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.413+6829G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086095 | ||||||
| chr12:122086098
|
A | C | 1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6832A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086098 | ||||||
| chr12:122086101
|
G | T | 1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6835G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086101 | ||||||
| chr12:122086106
|
T | G | 1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6840T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086106 | ||||||
| chr12:122086110
|
G | GAAGCCGG others(9): Show |
1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6844_413+6845i others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086110 | ||||||
| chr12:122086112
|
C | G | 1 | a0002c0002t0002g0277 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+6846C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086112 | ||||||
| chr12:122086161
|
TG | T | 3 | a0001c0001t0030g0056a0002c0002t0002g0277a0002c0005t0004g0233 | 3 | HG01169.hp2 HG03491.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.413+6898delG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122086161 | |||||
| chr12:122086175
|
C | G | 5 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(2): Show | 5 | HG02486.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+6909C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086175 | ||||||
| chr12:122086289
|
G | A | 1 | a0002c0005t0004g0279 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.413+7023G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086289 | ||||||
| chr12:122086322
|
GA | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.413+7057delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086322 | ||||||
| chr12:122086363
|
G | A | 11 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(8): Show | 11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+7097G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086363 | ||||||
| chr12:122086693
|
C | T | 1 | a0001c0001t0058g0348 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.413+7427C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086693 | ||||||
| chr12:122086876
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.413+7610A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086876 | ||||||
| chr12:122086963
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.413+7697A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086963 | ||||||
| chr12:122086991
|
A | G | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+7725A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086991 | ||||||
| chr12:122086995
|
G | A | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+7729G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086995 | ||||||
| chr12:122086996
|
C | T | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+7730C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122086996 | ||||||
| chr12:122087008
|
C | G | 1 | a0001c0001t0058g0348 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.413+7742C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087008 | ||||||
| chr12:122087020
|
G | C | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+7754G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087020 | ||||||
| chr12:122087021
|
T | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0147 | 4 | HG00099.hp2 HG00140.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+7755T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087021 | ||||||
| chr12:122087073
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.413+7807G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087073 | ||||||
| chr12:122087095
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+7829C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087095 | ||||||
| chr12:122087130
|
C | T | 12 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+7864C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087130 | ||||||
| chr12:122087237
|
C | T | 63 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.413+7971C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087237 | ||||||
| chr12:122087287
|
C | T | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+8021C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087287 | ||||||
| chr12:122087574
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.413+8308A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087574 | ||||||
| chr12:122087632
|
A | G | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+8366A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087632 | ||||||
| chr12:122087648
|
G | T | 1 | a0001c0001t0064g0146 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.413+8382G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087648 | ||||||
| chr12:122087858
|
G | GT | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+8597dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122087858 | |||||
| chr12:122087950
|
A | G | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+8684A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087950 | ||||||
| chr12:122087982
|
G | A | 1 | a0002c0002t0002g0344 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.413+8716G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122087982 | ||||||
| chr12:122088009
|
C | T | 12 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+8743C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088009 | ||||||
| chr12:122088130
|
C | T | 1 | a0002c0009t0070g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+8864C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088130 | ||||||
| chr12:122088131
|
G | A | 1 | a0002c0005t0046g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.413+8865G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088131 | ||||||
| chr12:122088135
|
A | G | 1 | a0002c0002t0002g0275 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.413+8869A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088135 | ||||||
| chr12:122088171
|
C | T | 1 | a0001c0001t0015g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.413+8905C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088171 | ||||||
| chr12:122088313
|
T | C | 1 | a0002c0002t0002g0245 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.413+9047T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088313 | ||||||
| chr12:122088381
|
T | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.413+9115T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088381 | ||||||
| chr12:122088470
|
G | A | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+9204G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088470 | ||||||
| chr12:122088533
|
A | G | 1 | a0002c0002t0016g0273 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.413+9267A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088533 | ||||||
| chr12:122088580
|
A | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+9314A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088580 | ||||||
| chr12:122088734
|
C | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+9468C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088734 | ||||||
| chr12:122088784
|
C | T | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413+9518C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088784 | ||||||
| chr12:122088943
|
G | A | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+9677G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122088943 | ||||||
| chr12:122089009
|
C | CA | 52 | a0001c0001t0001g0090a0001c0001t0001g0152a0001c0001t0001g0154others(49): Show | 52 | HG00280.hp1 HG00544.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.413+9766dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122089009 | |||||
| chr12:122089009
|
CA | C | 46 | a0001c0001t0001g0144a0001c0001t0001g0151a0001c0001t0001g0174others(43): Show | 46 | HG00323.hp1 HG00621.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.413+9766delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122089009 | |||||
| chr12:122089053
|
C | T | 1 | a0004c0007t0075g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413+9787C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122089053 | ||||||
| chr12:122089210
|
G | GAAGAAC | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+9945_413+9950d others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122089210 | |||||
| chr12:122089391
|
A | G | 1 | a0001c0001t0058g0348 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.413+10125A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122089391 | ||||||
| chr12:122089577
|
A | G | 7 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+10311A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122089577 | ||||||
| chr12:122089952
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.413+10686C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122089952 | ||||||
| chr12:122090080
|
T | C | 12 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+10814T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090080 | ||||||
| chr12:122090119
|
C | T | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.413+10853C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090119 | ||||||
| chr12:122090283
|
G | A | 2 | a0002c0002t0012g0210a0002c0002t0012g0211 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.413+11017G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090283 | ||||||
| chr12:122090294
|
G | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.413+11028G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090294 | ||||||
| chr12:122090357
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.413+11091T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090357 | ||||||
| chr12:122090369
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+11103T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090369 | ||||||
| chr12:122090408
|
ACT | A | 10 | a0001c0003t0003g0306a0001c0003t0003g0307a0001c0003t0003g0322others(7): Show | 10 | HG01361.hp2 HG01496.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+11147_413+1114 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122090408 | |||||
| chr12:122090419
|
A | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+11153A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090419 | ||||||
| chr12:122090496
|
CA | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.413+11242delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122090496 | |||||
| chr12:122090502
|
A | G | 2 | a0002c0002t0012g0213a0002c0002t0012g0214 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.413+11236A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090502 | ||||||
| chr12:122090554
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.413+11288A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090554 | ||||||
| chr12:122090577
|
A | G | 1 | a0004c0007t0019g0339 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413+11311A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122090577 | ||||||
| chr12:122091073
|
T | A | 1 | a0001c0003t0003g0305 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.413+11807T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091073 | ||||||
| chr12:122091193
|
G | A | 7 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+11927G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091193 | ||||||
| chr12:122091416
|
G | A | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+12150G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091416 | ||||||
| chr12:122091477
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.413+12211T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091477 | ||||||
| chr12:122091642
|
A | C | 11 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+12376A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091642 | ||||||
| chr12:122091700
|
A | T | 1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.413+12434A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091700 | ||||||
| chr12:122091761
|
C | T | 1 | a0004c0007t0019g0339 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413+12495C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122091761 | ||||||
| chr12:122092029
|
C | T | 12 | a0001c0001t0001g0147a0001c0008t0028g0014a0001c0008t0028g0016others(9): Show | 12 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+12763C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092029 | ||||||
| chr12:122092059
|
CCTTTCTT others(3): Show |
C | 2 | a0002c0002t0035g0271a0002c0002t0035g0276 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.413+12808_413+1281 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122092059 | |||||
| chr12:122092107
|
C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.413+12841C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092107 | ||||||
| chr12:122092160
|
C | T | 1 | a0007c0014t0019g0340 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.413+12894C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092160 | ||||||
| chr12:122092280
|
G | A | 3 | a0002c0002t0002g0246a0002c0002t0002g0247a0002c0002t0002g0248 | 3 | NA18953.hp1 NA18972.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.413+13014G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092280 | ||||||
| chr12:122092350
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.413+13084T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092350 | ||||||
| chr12:122092386
|
A | G | 1 | a0002c0010t0017g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.413+13120A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092386 | ||||||
| chr12:122092518
|
G | A | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413+13252G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092518 | ||||||
| chr12:122092742
|
A | G | 63 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.413+13476A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092742 | ||||||
| chr12:122092847
|
C | T | 223 | a0001c0001t0011g0050a0001c0001t0011g0052a0001c0001t0011g0054others(220): Show | 223 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.413+13581C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092847 | ||||||
| chr12:122092916
|
T | TGATGTGT others(11): Show |
1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.413+13659_413+1366 others(22): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122092916 | |||||
| chr12:122092916
|
T | TGATGTGT others(12): Show |
208 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(205): Show | 208 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.413+13659_413+1366 others(23): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122092916 | |||||
| chr12:122092925
|
T | TTGGTGTG others(12): Show |
1 | a0010c0016t0003g0289 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.413+13659_413+1366 others(23): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122092925 | ||||||
| chr12:122093034
|
GGT | G | 58 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.413+13777_413+1377 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093034 | |||||
| chr12:122093095
|
TGTGGTGT others(5): Show |
T | 183 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(180): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.413+13830_413+1384 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093095 | ||||||
| chr12:122093178
|
G | A | 1 | a0002c0002t0002g0275 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.413+13912G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093178 | ||||||
| chr12:122093256
|
A | C | 1 | a0002c0005t0009g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.413+13990A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093256 | ||||||
| chr12:122093260
|
Y | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.413+13994T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093260 | ||||||
| chr12:122093260
|
Y | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(12): Show | 15 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+13994C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093260 | ||||||
| chr12:122093276
|
A | G | 183 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(180): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.413+14010A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093276 | ||||||
| chr12:122093317
|
G | A | 80 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(77): Show | 80 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.413+14051G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093317 | ||||||
| chr12:122093461
|
A | G | 181 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(178): Show | 181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.413+14195A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093461 | ||||||
| chr12:122093464
|
T | C | 1 | a0002c0004t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.413+14198T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093464 | ||||||
| chr12:122093485
|
GGT | G | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+14229_413+1423 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093485 | |||||
| chr12:122093498
|
G | A | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+14232G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093498 | ||||||
| chr12:122093596
|
G | A | 7 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+14330G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093596 | ||||||
| chr12:122093677
|
A | G | 229 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0174others(226): Show | 229 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.413+14411A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093677 | ||||||
| chr12:122093697
|
TGGGGTGT others(10): Show |
T | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+14442_413+1445 others(21): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093697 | |||||
| chr12:122093765
|
T | G | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+14499T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093765 | ||||||
| chr12:122093767
|
T | G | 181 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(178): Show | 181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.413+14501T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093767 | ||||||
| chr12:122093769
|
T | G | 182 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(179): Show | 182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+14503T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093769 | ||||||
| chr12:122093791
|
TGTGTGTG others(3): Show |
T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+14536_413+1454 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093791 | |||||
| chr12:122093854
|
AGTGTCTG | A | 4 | a0002c0010t0017g0169a0002c0010t0017g0170a0002c0010t0017g0171others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+14593_413+1459 others(11): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093854 | |||||
| chr12:122093890
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.413+14624C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093890 | ||||||
| chr12:122093902
|
G | C | 2 | a0001c0001t0008g0026a0001c0001t0008g0086 | 2 | HG01167.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.413+14636G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093902 | ||||||
| chr12:122093927
|
TGTG | T | 81 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(78): Show | 81 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.413+14668_413+1467 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122093927 | |||||
| chr12:122093980
|
G | A | 182 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(179): Show | 182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+14714G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093980 | ||||||
| chr12:122093991
|
C | T | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+14725C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122093991 | ||||||
| chr12:122094001
|
TGTG | T | 12 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+14739_413+1474 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094001 | |||||
| chr12:122094095
|
G | T | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413+14829G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094095 | ||||||
| chr12:122094128
|
ATG | A | 58 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.413+14869_413+1487 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094128 | |||||
| chr12:122094176
|
GTGT | G | 12 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+14913_413+1491 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094176 | |||||
| chr12:122094192
|
TGTGTGTT others(1): Show |
T | 183 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(180): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.413+14933_413+1494 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094192 | |||||
| chr12:122094217
|
GGT | G | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+14958_413+1495 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094217 | |||||
| chr12:122094247
|
TG | T | 182 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(179): Show | 182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+14983delG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094247 | |||||
| chr12:122094389
|
GTGT | G | 4 | a0002c0005t0009g0235a0002c0005t0009g0237a0002c0005t0009g0238others(1): Show | 4 | HG01109.hp1 HG01934.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+15126_413+1512 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094389 | |||||
| chr12:122094391
|
G | T | 1 | a0002c0004t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.413+15125G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094391 | ||||||
| chr12:122094445
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+15179C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094445 | ||||||
| chr12:122094498
|
CTG | C | 170 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(167): Show | 170 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.413+15241_413+1524 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094498 | |||||
| chr12:122094516
|
GGT | G | 181 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(178): Show | 181 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.413+15259_413+1526 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094516 | |||||
| chr12:122094520
|
T | A | 1 | a0002c0004t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.413+15254T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094520 | ||||||
| chr12:122094550
|
G | T | 1 | a0002c0002t0002g0333 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.413+15284G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094550 | ||||||
| chr12:122094574
|
G | A | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+15308G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094574 | ||||||
| chr12:122094599
|
GTGT | G | 6 | a0002c0005t0009g0235a0002c0005t0009g0237a0002c0005t0009g0238others(3): Show | 6 | HG00323.hp1 HG01099.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+15337_413+1533 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094599 | |||||
| chr12:122094679
|
C | T | 5 | a0002c0002t0012g0210a0002c0002t0012g0211a0002c0002t0012g0212others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+15413C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094679 | ||||||
| chr12:122094681
|
A | G | 183 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(180): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.413+15415A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094681 | ||||||
| chr12:122094803
|
GGTGTGTT others(5): Show |
G | 1 | a0002c0002t0002g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.413+15555_413+1556 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122094803 | |||||
| chr12:122094919
|
G | T | 183 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(180): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.413+15653G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094919 | ||||||
| chr12:122094996
|
G | A | 12 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+15730G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094996 | ||||||
| chr12:122094996
|
G | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+15730G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122094996 | ||||||
| chr12:122095001
|
CTG | C | 183 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(180): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.413+15740_413+1574 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122095001 | |||||
| chr12:122095145
|
TGTGCGGT others(19): Show |
T | 63 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.413+15905_413+1593 others(30): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122095145 | |||||
| chr12:122095154
|
T | A | 1 | a0001c0003t0007g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+15888T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095154 | ||||||
| chr12:122095155
|
G | T | 1 | a0001c0003t0007g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+15889G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095155 | ||||||
| chr12:122095157
|
T | C | 1 | a0001c0003t0007g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+15891T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095157 | ||||||
| chr12:122095160
|
T | G | 1 | a0002c0004t0004g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.413+15894T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095160 | ||||||
| chr12:122095168
|
G | A | 1 | a0001c0001t0006g0100 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.413+15902G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095168 | ||||||
| chr12:122095171
|
A | T | 1 | a0001c0003t0007g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+15905A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095171 | ||||||
| chr12:122095176
|
G | A | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+15910G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095176 | ||||||
| chr12:122095189
|
G | A | 4 | a0002c0005t0009g0235a0002c0005t0009g0237a0002c0005t0009g0238others(1): Show | 4 | HG01109.hp1 HG01934.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+15923G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095189 | ||||||
| chr12:122095201
|
G | A | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+15935G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095201 | ||||||
| chr12:122095297
|
T | G | 1 | a0001c0001t0006g0334 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.413+16031T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095297 | ||||||
| chr12:122095297
|
T | TG | 18 | a0001c0001t0001g0101a0001c0001t0013g0349a0001c0001t0033g0163others(15): Show | 18 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.413+16038dupG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122095297 | |||||
| chr12:122095299
|
G | T | 3 | a0002c0002t0002g0200a0002c0002t0002g0270a0013c0021t0077g0010 | 3 | HG02523.hp2 HG03579.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.413+16033G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095299 | ||||||
| chr12:122095303
|
G | T | 1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.413+16037G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095303 | ||||||
| chr12:122095305
|
T | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+16039T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095305 | ||||||
| chr12:122095342
|
G | C | 210 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(207): Show | 210 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.413+16076G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095342 | ||||||
| chr12:122095478
|
G | A | 10 | a0001c0001t0011g0050a0001c0001t0011g0052a0001c0001t0011g0054others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+16212G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095478 | ||||||
| chr12:122095558
|
G | A | 1 | a0001c0003t0003g0311 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.413+16292G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095558 | ||||||
| chr12:122095675
|
CCTTTT | C | 12 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+16416_413+1642 others(9): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122095675 | |||||
| chr12:122095782
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+16516C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095782 | ||||||
| chr12:122095877
|
T | A | 12 | a0002c0002t0002g0198a0002c0002t0002g0199a0002c0002t0010g0017others(9): Show | 12 | HG00621.hp2 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+16611T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095877 | ||||||
| chr12:122095897
|
G | A | 46 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.413+16631G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095897 | ||||||
| chr12:122095951
|
G | C | 8 | a0003c0006t0001g0027a0003c0006t0001g0028a0003c0006t0001g0029others(5): Show | 8 | HG02257.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+16685G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095951 | ||||||
| chr12:122095959
|
G | A | 182 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(179): Show | 182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.413+16693G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122095959 | ||||||
| chr12:122096185
|
G | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.413+16919G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096185 | ||||||
| chr12:122096235
|
A | G | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+16969A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096235 | ||||||
| chr12:122096282
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.413+17016A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096282 | ||||||
| chr12:122096557
|
A | G | 1 | a0004c0007t0075g0338 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413+17291A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096557 | ||||||
| chr12:122096601
|
G | A | 10 | a0001c0001t0011g0050a0001c0001t0011g0052a0001c0001t0011g0054others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+17335G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096601 | ||||||
| chr12:122096775
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+17509G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096775 | ||||||
| chr12:122096881
|
G | A | 1 | a0001c0001t0011g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.413+17615G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096881 | ||||||
| chr12:122096925
|
G | A | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+17659G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122096925 | ||||||
| chr12:122097064
|
C | T | 1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.413+17798C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097064 | ||||||
| chr12:122097222
|
A | G | 1 | a0001c0001t0014g0153 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.413+17956A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097222 | ||||||
| chr12:122097239
|
C | T | 7 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+17973C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097239 | ||||||
| chr12:122097248
|
G | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.413+17982G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097248 | ||||||
| chr12:122097279
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+18013C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097279 | ||||||
| chr12:122097584
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0072 | 2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.413+18318G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097584 | ||||||
| chr12:122097594
|
CAG | C | 5 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+18331_413+1833 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097594 | |||||
| chr12:122097613
|
T | TA | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.413+18361dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097613 | |||||
| chr12:122097676
|
G | GT | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+18411dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097676 | |||||
| chr12:122097692
|
C | T | 4 | a0004c0007t0034g0335a0004c0007t0034g0336a0004c0007t0075g0338others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+18426C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097692 | ||||||
| chr12:122097746
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.413+18480G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097746 | ||||||
| chr12:122097846
|
T | TC | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0060others(135): Show | 140 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.413+18585dupC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097846 | |||||
| chr12:122097846
|
T | TCC | 8 | a0001c0001t0001g0058a0001c0001t0001g0150a0001c0001t0014g0067others(5): Show | 8 | HG01175.hp2 HG02738.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+18584_413+1858 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122097846 | |||||
| chr12:122097852
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+18586T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097852 | ||||||
| chr12:122097857
|
A | C | 1 | a0001c0001t0013g0349 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.413+18591A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097857 | ||||||
| chr12:122097891
|
G | C | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+18625G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097891 | ||||||
| chr12:122097946
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+18680T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097946 | ||||||
| chr12:122097982
|
T | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.413+18716T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122097982 | ||||||
| chr12:122098279
|
A | T | 1 | a0005c0012t0073g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.413+19013A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122098279 | ||||||
| chr12:122098924
|
G | A | 1 | a0001c0001t0060g0069 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.413+19658G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122098924 | ||||||
| chr12:122098971
|
C | T | 1 | a0002c0002t0040g0230 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.413+19705C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122098971 | ||||||
| chr12:122098980
|
G | A | 58 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.413+19714G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122098980 | ||||||
| chr12:122099234
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.413+19968A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099234 | ||||||
| chr12:122099252
|
A | G | 3 | a0002c0002t0002g0330a0002c0002t0002g0333a0002c0024t0002g0332 | 3 | HG02615.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.413+19986A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099252 | ||||||
| chr12:122099375
|
T | C | 1 | a0002c0002t0002g0250 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.413+20109T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099375 | ||||||
| chr12:122099443
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+20177C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099443 | ||||||
| chr12:122099451
|
G | A | 1 | a0002c0004t0068g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.413+20185G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099451 | ||||||
| chr12:122099616
|
A | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+20350A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099616 | ||||||
| chr12:122099720
|
A | G | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+20454A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099720 | ||||||
| chr12:122099744
|
A | G | 1 | a0001c0008t0028g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.413+20478A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099744 | ||||||
| chr12:122099823
|
T | A | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+20557T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122099823 | ||||||
| chr12:122100178
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.413+20912T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100178 | ||||||
| chr12:122100456
|
A | T | 1 | a0001c0001t0001g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413+21190A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100456 | ||||||
| chr12:122100518
|
T | C | 3 | a0002c0004t0005g0043a0002c0004t0005g0046a0002c0004t0066g0045 | 3 | HG02809.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+21252T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100518 | ||||||
| chr12:122100634
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.413+21368A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100634 | ||||||
| chr12:122100706
|
T | C | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+21440T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122100706 | ||||||
| chr12:122101036
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.413+21770A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101036 | ||||||
| chr12:122101037
|
TTATAA | T | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+21776_413+2178 others(9): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101037 | |||||
| chr12:122101106
|
C | T | 11 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+21840C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101106 | ||||||
| chr12:122101144
|
G | A | 1 | a0004c0007t0019g0339 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413+21878G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101144 | ||||||
| chr12:122101362
|
A | G | 1 | a0001c0001t0006g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.413+22096A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101362 | ||||||
| chr12:122101374
|
A | G | 10 | a0001c0001t0011g0050a0001c0001t0011g0052a0001c0001t0011g0054others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+22108A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101374 | ||||||
| chr12:122101443
|
A | G | 2 | a0002c0002t0027g0012a0002c0002t0027g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.413+22177A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101443 | ||||||
| chr12:122101449
|
C | CT | 69 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(66): Show | 69 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.413+22192dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101449 | |||||
| chr12:122101526
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.413+22260T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101526 | ||||||
| chr12:122101554
|
ATTTATTT others(6): Show |
A | 3 | a0002c0002t0026g0187a0002c0002t0026g0202a0002c0002t0045g0203 | 3 | HG02109.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.413+22292_413+2230 others(17): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101554 | |||||
| chr12:122101566
|
A | T | 5 | a0001c0003t0003g0318a0001c0003t0003g0319a0001c0003t0003g0320others(2): Show | 5 | HG00741.hp2 HG01943.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+22300A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101566 | ||||||
| chr12:122101566
|
AT | A | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.413+22307delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101566 | |||||
| chr12:122101570
|
T | A | 11 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(8): Show | 11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+22304T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101570 | ||||||
| chr12:122101573
|
T | C | 1 | a0002c0002t0002g0281 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.413+22307T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101573 | ||||||
| chr12:122101574
|
C | CT | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+22317dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101574 | |||||
| chr12:122101574
|
C | T | 1 | a0002c0002t0002g0281 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.413+22308C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101574 | ||||||
| chr12:122101584
|
C | CT | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.413+22332dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122101584 | |||||
| chr12:122101584
|
C | T | 1 | a0002c0002t0002g0281 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.413+22318C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101584 | ||||||
| chr12:122101605
|
G | A | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+22339G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101605 | ||||||
| chr12:122101641
|
C | T | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+22375C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101641 | ||||||
| chr12:122101673
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+22407C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101673 | ||||||
| chr12:122101674
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.413+22408A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101674 | ||||||
| chr12:122101732
|
C | CT | 11 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(8): Show | 11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+22466_413+2246 others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101732 | ||||||
| chr12:122101733
|
A | C | 11 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(8): Show | 11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+22467A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101733 | ||||||
| chr12:122101743
|
G | A | 1 | a0002c0002t0002g0281 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.413+22477G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101743 | ||||||
| chr12:122101778
|
A | G | 10 | a0001c0001t0011g0050a0001c0001t0011g0052a0001c0001t0011g0054others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+22512A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101778 | ||||||
| chr12:122101858
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.413+22592C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122101858 | ||||||
| chr12:122102119
|
G | A | 1 | a0002c0002t0010g0017 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.413+22853G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102119 | ||||||
| chr12:122102370
|
G | A | 1 | a0001c0003t0003g0286 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.413+23104G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102370 | ||||||
| chr12:122102413
|
G | C | 2 | a0001c0001t0033g0163a0001c0001t0033g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+23147G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102413 | ||||||
| chr12:122102430
|
A | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+23164A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102430 | ||||||
| chr12:122102645
|
T | C | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413+23379T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102645 | ||||||
| chr12:122102754
|
C | G | 3 | a0002c0002t0002g0199a0002c0002t0016g0177a0002c0002t0016g0186 | 3 | HG01070.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.413+23488C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102754 | ||||||
| chr12:122102909
|
G | A | 1 | a0001c0003t0050g0312 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.413+23643G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102909 | ||||||
| chr12:122102958
|
T | G | 1 | a0002c0009t0070g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+23692T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102958 | ||||||
| chr12:122102998
|
C | T | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+23732C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122102998 | ||||||
| chr12:122103026
|
C | T | 1 | a0007c0014t0019g0340 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.413+23760C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103026 | ||||||
| chr12:122103054
|
A | G | 70 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.413+23788A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103054 | ||||||
| chr12:122103130
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+23864A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103130 | ||||||
| chr12:122103175
|
ATATG | A | 51 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.413+23933_413+2393 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103175 | |||||
| chr12:122103187
|
G | A | 1 | a0002c0002t0040g0230 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.413+23921G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103187 | ||||||
| chr12:122103194
|
T | C | 1 | a0002c0002t0002g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413+23928T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103194 | ||||||
| chr12:122103195
|
GTATGTAT others(1): Show |
G | 8 | a0002c0002t0002g0283a0002c0002t0026g0187a0002c0002t0026g0202others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+23933_413+2394 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103195 | |||||
| chr12:122103199
|
G | T | 2 | a0002c0002t0002g0223a0002c0002t0035g0276 | 2 | HG03239.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.413+23933G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103199 | ||||||
| chr12:122103199
|
GTATT | G | 24 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(21): Show | 24 | HG01261.hp2 HG01884.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+23971_413+2397 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | |||||
| chr12:122103199
|
GTATTTAT others(1): Show |
G | 88 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0008g0148others(85): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.413+23967_413+2397 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | |||||
| chr12:122103199
|
GTATTTAT others(5): Show |
G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.413+23963_413+2397 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | |||||
| chr12:122103199
|
GTATTTAT others(9): Show |
G | 1 | a0002c0004t0005g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.413+23959_413+2397 others(20): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | |||||
| chr12:122103199
|
GTATTTAT others(13): Show |
G | 7 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+23955_413+2397 others(24): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | |||||
| chr12:122103199
|
GTATTTAT others(17): Show |
G | 1 | a0001c0001t0014g0133 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.413+23951_413+2397 others(28): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103199 | |||||
| chr12:122103203
|
T | G | 4 | a0001c0001t0033g0163a0001c0001t0033g0164a0001c0001t0058g0348others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+23937T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103203 | ||||||
| chr12:122103207
|
T | G | 19 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(16): Show | 19 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+23941T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103207 | ||||||
| chr12:122103211
|
T | G | 25 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0008g0148others(22): Show | 25 | HG00099.hp1 HG00738.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.413+23945T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103211 | ||||||
| chr12:122103215
|
T | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.413+23949T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103215 | ||||||
| chr12:122103219
|
T | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.413+23953T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103219 | ||||||
| chr12:122103223
|
T | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.413+23957T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103223 | ||||||
| chr12:122103227
|
T | G | 13 | a0001c0001t0033g0164a0002c0002t0005g0025a0002c0002t0005g0039others(10): Show | 13 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+23961T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103227 | ||||||
| chr12:122103231
|
T | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.413+23965T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103231 | ||||||
| chr12:122103246
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+23980G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103246 | ||||||
| chr12:122103521
|
C | CT | 20 | a0001c0003t0003g0303a0001c0003t0003g0315a0001c0003t0003g0326others(17): Show | 20 | HG01099.hp1 HG01981.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-23718dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103521 | |||||
| chr12:122103521
|
CT | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.414-23718delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103521 | |||||
| chr12:122103584
|
G | A | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-23672G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103584 | ||||||
| chr12:122103690
|
TTG | T | 7 | a0001c0003t0003g0004a0001c0003t0003g0308a0001c0003t0003g0310others(4): Show | 7 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-23564_414-2356 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103690 | |||||
| chr12:122103694
|
A | AT | 11 | a0002c0002t0002g0247a0002c0002t0002g0344a0002c0002t0010g0017others(8): Show | 11 | HG00323.hp2 HG00621.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-23546dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103694 | |||||
| chr12:122103694
|
A | T | 7 | a0001c0003t0003g0004a0001c0003t0003g0308a0001c0003t0003g0310others(4): Show | 7 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-23562A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103694 | ||||||
| chr12:122103746
|
G | A | 63 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.414-23510G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103746 | ||||||
| chr12:122103776
|
G | A | 3 | a0001c0003t0003g0318a0001c0003t0003g0319a0001c0003t0003g0320 | 3 | HG00741.hp2 HG01943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.414-23480G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103776 | ||||||
| chr12:122103840
|
G | GT | 25 | a0001c0008t0028g0014a0001c0008t0028g0016a0001c0008t0056g0217others(22): Show | 25 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.414-23401dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103840 | |||||
| chr12:122103840
|
GT | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.414-23401delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122103840 | |||||
| chr12:122103844
|
T | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-23412T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103844 | ||||||
| chr12:122103921
|
C | T | 3 | a0002c0002t0010g0017a0002c0002t0010g0022a0002c0002t0010g0023 | 3 | HG02027.hp2 NA18612.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.414-23335C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103921 | ||||||
| chr12:122103942
|
G | A | 32 | a0002c0002t0021g0181a0002c0004t0003g0176a0002c0004t0003g0183others(29): Show | 32 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.414-23314G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122103942 | ||||||
| chr12:122104026
|
A | G | 1 | a0001c0008t0048g0295 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.414-23230A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104026 | ||||||
| chr12:122104194
|
A | ACAAGTGT others(3): Show |
2 | a0001c0001t0033g0163a0001c0001t0033g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-23061_414-2305 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104194 | |||||
| chr12:122104424
|
G | A | 1 | a0001c0001t0031g0343 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.414-22832G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104424 | ||||||
| chr12:122104485
|
T | A | 3 | a0002c0002t0002g0223a0002c0002t0002g0251a0002c0002t0002g0256 | 3 | NA18952.hp1 NA19001.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.414-22771T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104485 | ||||||
| chr12:122104509
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-22747G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104509 | ||||||
| chr12:122104537
|
C | A | 1 | a0002c0002t0035g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414-22719C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104537 | ||||||
| chr12:122104575
|
C | CT | 7 | a0001c0003t0003g0302a0001c0003t0003g0311a0002c0002t0002g0247others(4): Show | 7 | HG00673.hp1 HG01952.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-22659dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104575 | |||||
| chr12:122104575
|
CT | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-22659delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104575 | |||||
| chr12:122104575
|
CTT | C | 15 | a0001c0001t0008g0165a0001c0001t0030g0057a0002c0002t0042g0018others(12): Show | 15 | HG01069.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-22660_414-2265 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104575 | |||||
| chr12:122104575
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0079 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.414-22672_414-2265 others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122104575 | |||||
| chr12:122104602
|
C | T | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.414-22654C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104602 | ||||||
| chr12:122104609
|
T | G | 2 | a0001c0001t0030g0056a0001c0001t0030g0057 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.414-22647T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104609 | ||||||
| chr12:122104653
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0015g0175 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.414-22603C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104653 | ||||||
| chr12:122104675
|
G | A | 2 | a0002c0002t0021g0181a0002c0004t0021g0182 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.414-22581G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104675 | ||||||
| chr12:122104681
|
G | A | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-22575G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104681 | ||||||
| chr12:122104715
|
G | T | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-22541G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104715 | ||||||
| chr12:122104736
|
C | T | 1 | a0002c0005t0009g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414-22520C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104736 | ||||||
| chr12:122104807
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-22449C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104807 | ||||||
| chr12:122104848
|
A | G | 70 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.414-22408A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104848 | ||||||
| chr12:122104987
|
G | A | 20 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(17): Show | 20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-22269G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122104987 | ||||||
| chr12:122105234
|
T | C | 1 | a0001c0001t0058g0348 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.414-22022T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105234 | ||||||
| chr12:122105278
|
G | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.414-21978G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105278 | ||||||
| chr12:122105320
|
A | AT | 6 | a0001c0001t0011g0054a0001c0001t0011g0059a0001c0001t0011g0062others(3): Show | 6 | HG00609.hp2 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-21926dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122105320 | |||||
| chr12:122105350
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.414-21906C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105350 | ||||||
| chr12:122105353
|
G | GT | 11 | a0001c0001t0006g0128a0001c0001t0014g0127a0001c0001t0044g0048others(8): Show | 11 | HG02015.hp2 HG02080.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-21893dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122105353 | |||||
| chr12:122105377
|
C | T | 1 | a0002c0004t0005g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.414-21879C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105377 | ||||||
| chr12:122105564
|
C | T | 1 | a0002c0002t0002g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.414-21692C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105564 | ||||||
| chr12:122105628
|
C | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0147 | 4 | HG00099.hp2 HG00140.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-21628C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105628 | ||||||
| chr12:122105633
|
G | A | 3 | a0002c0004t0005g0043a0002c0004t0005g0046a0002c0004t0066g0045 | 3 | HG02809.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.414-21623G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105633 | ||||||
| chr12:122105791
|
A | C | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-21465A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105791 | ||||||
| chr12:122105821
|
C | G | 2 | a0001c0001t0033g0163a0001c0001t0033g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-21435C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105821 | ||||||
| chr12:122105918
|
G | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-21338G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105918 | ||||||
| chr12:122105944
|
G | C | 1 | a0007c0014t0019g0340 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.414-21312G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105944 | ||||||
| chr12:122105956
|
A | C | 1 | a0002c0009t0011g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.414-21300A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105956 | ||||||
| chr12:122105979
|
C | T | 1 | a0002c0004t0020g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-21277C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122105979 | ||||||
| chr12:122106016
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-21240T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106016 | ||||||
| chr12:122106037
|
C | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-21219C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106037 | ||||||
| chr12:122106090
|
A | G | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-21166A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106090 | ||||||
| chr12:122106176
|
A | G | 21 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(18): Show | 21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.414-21080A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106176 | ||||||
| chr12:122106252
|
T | TTC | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-21002_414-2100 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106252 | |||||
| chr12:122106440
|
ATTGTCAC others(4): Show |
A | 1 | a0002c0009t0070g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414-20805_414-2079 others(15): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106440 | |||||
| chr12:122106491
|
G | T | 4 | a0001c0003t0003g0004a0001c0003t0003g0308a0001c0003t0003g0310others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-20765G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106491 | ||||||
| chr12:122106582
|
G | A | 7 | a0002c0002t0026g0187a0002c0002t0026g0202a0002c0002t0045g0203others(4): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-20674G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106582 | ||||||
| chr12:122106588
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.414-20668G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106588 | ||||||
| chr12:122106595
|
C | CT | 18 | a0001c0001t0013g0035a0001c0003t0003g0303a0001c0003t0003g0307others(15): Show | 18 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.414-20637dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106595 | |||||
| chr12:122106595
|
C | CTT | 11 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(8): Show | 11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-20638_414-2063 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106595 | |||||
| chr12:122106595
|
CT | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.414-20637delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106595 | |||||
| chr12:122106595
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0011g0050a0001c0001t0011g0052a0001c0001t0011g0054others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-20644_414-2063 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122106595 | |||||
| chr12:122106746
|
C | T | 1 | a0002c0002t0002g0333 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.414-20510C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106746 | ||||||
| chr12:122106754
|
T | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-20502T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106754 | ||||||
| chr12:122106819
|
C | A | 3 | a0002c0002t0026g0187a0002c0002t0026g0202a0002c0002t0045g0203 | 3 | HG02109.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.414-20437C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106819 | ||||||
| chr12:122106860
|
C | A | 1 | a0001c0001t0006g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.414-20396C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106860 | ||||||
| chr12:122106952
|
G | C | 10 | a0001c0003t0003g0306a0001c0003t0003g0307a0001c0003t0003g0322others(7): Show | 10 | HG01361.hp2 HG01496.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-20304G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106952 | ||||||
| chr12:122106984
|
G | A | 11 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0109others(8): Show | 11 | HG00738.hp2 HG01106.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-20272G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122106984 | ||||||
| chr12:122107007
|
C | T | 20 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0075others(17): Show | 20 | HG00597.hp1 HG02040.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-20249C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107007 | ||||||
| chr12:122107204
|
T | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-20052T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107204 | ||||||
| chr12:122107466
|
T | TG | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-19789dupG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122107466 | |||||
| chr12:122107556
|
C | G | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.414-19700C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107556 | ||||||
| chr12:122107602
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0082a0001c0001t0001g0123 | 3 | HG01256.hp1 HG01258.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.414-19654A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107602 | ||||||
| chr12:122107944
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-19312C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122107944 | ||||||
| chr12:122108140
|
C | T | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-19116C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108140 | ||||||
| chr12:122108346
|
C | T | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-18910C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108346 | ||||||
| chr12:122108367
|
C | CA | 16 | a0001c0003t0003g0287a0001c0003t0003g0296a0001c0003t0003g0308others(13): Show | 16 | HG01074.hp2 HG01433.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.414-18868dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122108367 | |||||
| chr12:122108367
|
CA | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.414-18868delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122108367 | |||||
| chr12:122108495
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.414-18761C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108495 | ||||||
| chr12:122108693
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.414-18563G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108693 | ||||||
| chr12:122108763
|
G | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-18493G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122108763 | ||||||
| chr12:122109224
|
A | T | 1 | a0002c0004t0021g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.414-18032A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109224 | ||||||
| chr12:122109311
|
C | T | 1 | a0002c0004t0004g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414-17945C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109311 | ||||||
| chr12:122109384
|
A | C | 21 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(18): Show | 21 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.414-17872A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109384 | ||||||
| chr12:122109486
|
A | G | 63 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.414-17770A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109486 | ||||||
| chr12:122109697
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-17559C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109697 | ||||||
| chr12:122109702
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-17554T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109702 | ||||||
| chr12:122109982
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.414-17274G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122109982 | ||||||
| chr12:122110026
|
T | C | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.414-17230T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110026 | ||||||
| chr12:122110191
|
G | A | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-17065G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110191 | ||||||
| chr12:122110299
|
T | A | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-16957T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110299 | ||||||
| chr12:122110348
|
C | T | 1 | a0002c0004t0020g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-16908C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110348 | ||||||
| chr12:122110374
|
G | A | 2 | a0002c0004t0005g0015a0002c0004t0067g0009 | 2 | NA18969.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.414-16882G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110374 | ||||||
| chr12:122110444
|
C | T | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-16812C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110444 | ||||||
| chr12:122110538
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-16718C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110538 | ||||||
| chr12:122110544
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0007g0346 | 3 | HG02735.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.414-16712C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110544 | ||||||
| chr12:122110638
|
G | A | 1 | a0002c0004t0020g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-16618G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110638 | ||||||
| chr12:122110806
|
A | G | 3 | a0002c0002t0002g0245a0002c0002t0002g0267a0002c0002t0002g0272 | 3 | HG01975.hp2 HG01993.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.414-16450A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110806 | ||||||
| chr12:122110844
|
A | G | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-16412A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110844 | ||||||
| chr12:122110847
|
G | A | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-16409G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110847 | ||||||
| chr12:122110884
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0075 | 2 | HG00597.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.414-16372T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110884 | ||||||
| chr12:122110893
|
T | C | 2 | a0001c0001t0001g0150a0002c0004t0020g0191 | 2 | HG02258.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.414-16363T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110893 | ||||||
| chr12:122110902
|
C | A | 1 | a0002c0009t0070g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414-16354C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122110902 | ||||||
| chr12:122111071
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-16185T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111071 | ||||||
| chr12:122111076
|
C | CA | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.414-16162dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122111076 | |||||
| chr12:122111076
|
CA | C | 63 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(60): Show | 63 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.414-16162delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122111076 | |||||
| chr12:122111335
|
A | G | 1 | a0001c0001t0058g0348 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.414-15921A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111335 | ||||||
| chr12:122111564
|
C | G | 2 | a0001c0001t0033g0163a0001c0001t0033g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-15692C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111564 | ||||||
| chr12:122111601
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-15655C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111601 | ||||||
| chr12:122111932
|
A | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-15324A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122111932 | ||||||
| chr12:122112077
|
G | A | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-15179G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112077 | ||||||
| chr12:122112136
|
T | C | 2 | a0003c0006t0001g0028a0003c0006t0001g0029 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.414-15120T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112136 | ||||||
| chr12:122112351
|
T | C | 1 | a0002c0002t0012g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414-14905T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112351 | ||||||
| chr12:122112399
|
G | A | 1 | a0003c0006t0001g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.414-14857G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112399 | ||||||
| chr12:122112516
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0130 | 2 | NA18947.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.414-14740G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112516 | ||||||
| chr12:122112519
|
C | T | 8 | a0003c0006t0001g0027a0003c0006t0001g0028a0003c0006t0001g0029others(5): Show | 8 | HG02257.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-14737C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112519 | ||||||
| chr12:122112527
|
G | A | 7 | a0002c0004t0005g0005a0002c0004t0005g0006a0002c0004t0005g0007others(4): Show | 7 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-14729G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112527 | ||||||
| chr12:122112576
|
G | A | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-14680G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112576 | ||||||
| chr12:122112740
|
G | A | 1 | a0002c0002t0002g0274 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.414-14516G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112740 | ||||||
| chr12:122112863
|
T | C | 1 | a0002c0004t0049g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.414-14393T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112863 | ||||||
| chr12:122112976
|
A | AG | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-14280_414-1427 others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122112976 | ||||||
| chr12:122113366
|
C | G | 2 | a0002c0002t0021g0181a0002c0004t0021g0182 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.414-13890C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113366 | ||||||
| chr12:122113464
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-13792C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113464 | ||||||
| chr12:122113513
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.414-13743C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113513 | ||||||
| chr12:122113681
|
C | CT | 6 | a0001c0003t0003g0288a0001c0003t0047g0294a0001c0008t0048g0295others(3): Show | 6 | HG00597.hp2 HG02135.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-13554dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | |||||
| chr12:122113681
|
C | CTTTT | 6 | a0004c0007t0019g0339a0004c0007t0075g0338a0004c0007t0076g0337others(3): Show | 6 | HG01099.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-13557_414-1355 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | |||||
| chr12:122113681
|
C | CTTTTT | 14 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.414-13558_414-1355 others(9): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | |||||
| chr12:122113681
|
C | CTTTTTT | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.414-13559_414-1355 others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | |||||
| chr12:122113681
|
C | CTTTTTTT | 38 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0001g0081others(35): Show | 38 | HG00621.hp1 HG00735.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.414-13560_414-1355 others(11): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | |||||
| chr12:122113681
|
CT | C | 84 | a0001c0003t0003g0297a0001c0008t0028g0014a0001c0008t0028g0016others(81): Show | 84 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.414-13554delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | |||||
| chr12:122113681
|
CTT | C | 7 | a0001c0008t0056g0217a0002c0002t0002g0225a0002c0002t0012g0210others(4): Show | 7 | HG01169.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-13555_414-1355 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113681 | |||||
| chr12:122113704
|
A | G | 1 | a0002c0005t0004g0279 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.414-13552A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113704 | ||||||
| chr12:122113714
|
T | A | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-13542T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113714 | ||||||
| chr12:122113747
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-13509C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113747 | ||||||
| chr12:122113798
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.414-13458C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113798 | ||||||
| chr12:122113927
|
C | T | 1 | a0001c0001t0011g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.414-13329C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113927 | ||||||
| chr12:122113928
|
G | A | 1 | a0001c0001t0064g0146 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.414-13328G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113928 | ||||||
| chr12:122113981
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0072 | 2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.414-13275G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122113981 | ||||||
| chr12:122113984
|
C | CT | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.414-13254dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113984 | |||||
| chr12:122113984
|
C | CTT | 9 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0006g0134others(6): Show | 9 | HG00544.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-13255_414-1325 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113984 | |||||
| chr12:122113984
|
CT | C | 7 | a0001c0008t0056g0217a0002c0002t0002g0344a0002c0002t0012g0210others(4): Show | 7 | HG00323.hp2 HG01516.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-13254delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122113984 | |||||
| chr12:122114047
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-13209A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114047 | ||||||
| chr12:122114274
|
C | A | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-12982C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114274 | ||||||
| chr12:122114291
|
C | A | 7 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-12965C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114291 | ||||||
| chr12:122114394
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-12862T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114394 | ||||||
| chr12:122114473
|
A | G | 28 | a0002c0004t0003g0218a0002c0004t0003g0219a0002c0004t0004g0189others(25): Show | 28 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.414-12783A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114473 | ||||||
| chr12:122114495
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-12761T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114495 | ||||||
| chr12:122114554
|
G | A | 1 | a0002c0004t0020g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.414-12702G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114554 | ||||||
| chr12:122114559
|
G | A | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-12697G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114559 | ||||||
| chr12:122114668
|
C | T | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-12588C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114668 | ||||||
| chr12:122114689
|
C | T | 1 | a0002c0005t0004g0233 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.414-12567C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114689 | ||||||
| chr12:122114712
|
T | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-12544T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114712 | ||||||
| chr12:122114737
|
C | CT | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-12501dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122114737 | |||||
| chr12:122114737
|
C | CTT | 6 | a0001c0001t0006g0103a0001c0001t0006g0128a0001c0001t0014g0153others(3): Show | 6 | HG01175.hp2 HG02055.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-12502_414-1250 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122114737 | |||||
| chr12:122114755
|
T | G | 5 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(2): Show | 5 | HG02486.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-12501T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114755 | ||||||
| chr12:122114757
|
G | T | 5 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(2): Show | 5 | HG02486.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-12499G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114757 | ||||||
| chr12:122114758
|
T | TTG | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.414-12498_414-1249 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114758 | ||||||
| chr12:122114759
|
G | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0007g0346 | 3 | HG02735.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.414-12497G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114759 | ||||||
| chr12:122114764
|
G | T | 1 | a0003c0006t0015g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414-12492G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114764 | ||||||
| chr12:122114814
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-12442C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114814 | ||||||
| chr12:122114902
|
C | T | 1 | a0002c0002t0002g0282 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.414-12354C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122114902 | ||||||
| chr12:122115006
|
C | G | 20 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(17): Show | 20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-12250C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115006 | ||||||
| chr12:122115036
|
C | T | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.414-12220C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115036 | ||||||
| chr12:122115249
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-12007C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115249 | ||||||
| chr12:122115287
|
C | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-11969C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115287 | ||||||
| chr12:122115294
|
A | G | 20 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(17): Show | 20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-11962A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115294 | ||||||
| chr12:122115309
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-11947T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115309 | ||||||
| chr12:122115388
|
G | T | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-11868G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115388 | ||||||
| chr12:122115416
|
C | T | 4 | a0001c0001t0033g0163a0001c0001t0033g0164a0001c0003t0003g0317others(1): Show | 4 | HG02055.hp2 HG02129.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-11840C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115416 | ||||||
| chr12:122115461
|
C | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-11795C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115461 | ||||||
| chr12:122115536
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-11720G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115536 | ||||||
| chr12:122115581
|
T | G | 2 | a0002c0002t0027g0012a0002c0002t0027g0013 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.414-11675T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115581 | ||||||
| chr12:122115587
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.414-11669T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115587 | ||||||
| chr12:122115587
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.414-11669T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115587 | ||||||
| chr12:122115588
|
C | A | 1 | a0001c0001t0001g0132 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.414-11668C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115588 | ||||||
| chr12:122115588
|
C | CA | 173 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(170): Show | 173 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.414-11651dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | |||||
| chr12:122115588
|
C | CAA | 6 | a0001c0001t0008g0026a0001c0001t0014g0127a0001c0019t0001g0111others(3): Show | 6 | HG01167.hp2 HG01496.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-11652_414-1165 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | |||||
| chr12:122115588
|
C | CAAA | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.414-11653_414-1165 others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | |||||
| chr12:122115588
|
C | CAAAA | 6 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0006g0118others(3): Show | 6 | HG02135.hp2 HG02738.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-11654_414-1165 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | |||||
| chr12:122115588
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0013g0036a0001c0001t0013g0037a0001c0001t0013g0349others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-11660_414-1165 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | |||||
| chr12:122115588
|
C | CAAAAAAA others(4): Show |
9 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(6): Show | 9 | HG02809.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-11661_414-1165 others(15): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | |||||
| chr12:122115588
|
C | CAAAAAAA others(5): Show |
9 | a0002c0004t0005g0042a0002c0004t0005g0168a0002c0004t0068g0173others(6): Show | 9 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-11662_414-1165 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | |||||
| chr12:122115588
|
C | CAAAAAAA others(6): Show |
2 | a0002c0004t0066g0045a0004c0007t0075g0338 | 2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.414-11663_414-1165 others(17): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122115588 | |||||
| chr12:122115610
|
A | G | 1 | a0001c0001t0058g0348 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.414-11646A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115610 | ||||||
| chr12:122115966
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-11290A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115966 | ||||||
| chr12:122115985
|
A | G | 1 | a0002c0002t0035g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414-11271A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122115985 | ||||||
| chr12:122116019
|
C | A | 13 | a0002c0005t0004g0233a0002c0005t0004g0236a0002c0005t0004g0239others(10): Show | 13 | HG00323.hp1 HG01069.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-11237C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116019 | ||||||
| chr12:122116053
|
A | AAC | 70 | a0001c0001t0058g0348a0001c0003t0003g0299a0001c0003t0020g0325others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.414-11169_414-1116 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
A | AACAC | 16 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(13): Show | 16 | HG01243.hp2 HG01261.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.414-11171_414-1116 others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
A | AACACACA others(3): Show |
5 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-11177_414-1116 others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
A | AACACACA others(5): Show |
4 | a0002c0004t0005g0043a0002c0004t0005g0046a0002c0004t0005g0168others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-11179_414-1116 others(16): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
A | AACACACA others(7): Show |
6 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0004t0005g0044others(3): Show | 6 | HG02145.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-11181_414-1116 others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
A | AACACACA others(9): Show |
1 | a0004c0007t0019g0339 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.414-11183_414-1116 others(20): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
A | AACACACA others(11): Show |
6 | a0004c0007t0034g0335a0004c0007t0034g0336a0004c0007t0075g0338others(3): Show | 6 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-11185_414-1116 others(22): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
A | AACACACA others(17): Show |
1 | a0002c0009t0070g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414-11191_414-1116 others(28): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
AAC | A | 3 | a0002c0010t0017g0170a0002c0010t0017g0171a0002c0010t0017g0172 | 3 | HG01891.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.414-11169_414-1116 others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
AACACAC | A | 3 | a0001c0001t0001g0174a0001c0001t0014g0133a0001c0001t0015g0175 | 3 | HG01257.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.414-11173_414-1116 others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116053
|
AACACACA others(1): Show |
A | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-11175_414-1116 others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116053 | |||||
| chr12:122116180
|
C | T | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-11076C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116180 | ||||||
| chr12:122116256
|
A | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-11000A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116256 | ||||||
| chr12:122116281
|
G | GT | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-10966dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122116281 | |||||
| chr12:122116421
|
T | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-10835T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116421 | ||||||
| chr12:122116437
|
C | A | 8 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0106others(5): Show | 8 | HG00280.hp1 HG00735.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-10819C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116437 | ||||||
| chr12:122116693
|
A | G | 1 | a0002c0002t0041g0266 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.414-10563A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116693 | ||||||
| chr12:122116742
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-10514A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122116742 | ||||||
| chr12:122117103
|
C | T | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.414-10153C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122117103 | ||||||
| chr12:122117380
|
A | G | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.414-9876A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122117380 | ||||||
| chr12:122117626
|
G | C | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-9630G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122117626 | ||||||
| chr12:122117758
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-9498G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122117758 | ||||||
| chr12:122118053
|
T | A | 1 | a0001c0003t0003g0305 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.414-9203T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118053 | ||||||
| chr12:122118094
|
C | T | 1 | a0002c0002t0035g0271 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.414-9162C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118094 | ||||||
| chr12:122118263
|
A | G | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-8993A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118263 | ||||||
| chr12:122118270
|
A | AT | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.414-8983dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122118270 | |||||
| chr12:122118352
|
C | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.414-8904C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118352 | ||||||
| chr12:122118387
|
C | T | 2 | a0002c0002t0023g0264a0012c0022t0023g0265 | 2 | HG02155.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.414-8869C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118387 | ||||||
| chr12:122118392
|
T | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8864T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118392 | ||||||
| chr12:122118395
|
A | G | 20 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(17): Show | 20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-8861A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118395 | ||||||
| chr12:122118576
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8680A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118576 | ||||||
| chr12:122118709
|
G | A | 1 | a0008c0020t0019g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-8547G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118709 | ||||||
| chr12:122118779
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8477C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118779 | ||||||
| chr12:122118845
|
C | CA | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-8398dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122118845 | |||||
| chr12:122118866
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.414-8390T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118866 | ||||||
| chr12:122118895
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.414-8361G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118895 | ||||||
| chr12:122118932
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8324C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118932 | ||||||
| chr12:122118933
|
G | A | 1 | a0002c0004t0003g0183 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.414-8323G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118933 | ||||||
| chr12:122118949
|
G | A | 4 | a0001c0001t0001g0084a0001c0001t0001g0113a0001c0001t0001g0121others(1): Show | 4 | HG01123.hp2 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-8307G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118949 | ||||||
| chr12:122118967
|
C | G | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-8289C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118967 | ||||||
| chr12:122118993
|
C | T | 7 | a0001c0001t0011g0054a0001c0001t0011g0059a0001c0001t0011g0062others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-8263C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122118993 | ||||||
| chr12:122119016
|
A | T | 6 | a0001c0001t0008g0141a0001c0001t0018g0087a0001c0001t0018g0088others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-8240A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119016 | ||||||
| chr12:122119034
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-8222C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119034 | ||||||
| chr12:122119037
|
C | T | 2 | a0002c0002t0041g0266a0002c0005t0004g0236 | 2 | HG01361.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.414-8219C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119037 | ||||||
| chr12:122119167
|
C | CA | 4 | a0001c0001t0033g0163a0001c0001t0033g0164a0001c0003t0047g0294others(1): Show | 4 | HG02055.hp2 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-8082dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122119167 | |||||
| chr12:122119175
|
CAAACA | C | 13 | a0002c0002t0002g0344a0002c0002t0005g0025a0002c0002t0005g0039others(10): Show | 13 | HG00323.hp2 HG01243.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.414-8058_414-8054d others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122119175 | |||||
| chr12:122119190
|
AAAACAAA others(2): Show |
A | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-8058_414-8050d others(11): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122119190 | |||||
| chr12:122119315
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-7941G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119315 | ||||||
| chr12:122119342
|
T | A | 5 | a0001c0001t0011g0054a0001c0001t0011g0059a0001c0001t0011g0062others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-7914T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119342 | ||||||
| chr12:122119431
|
G | A | 8 | a0002c0002t0016g0273a0004c0007t0019g0339a0004c0007t0034g0335others(5): Show | 8 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-7825G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119431 | ||||||
| chr12:122119548
|
C | T | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-7708C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119548 | ||||||
| chr12:122119552
|
C | T | 3 | a0002c0004t0005g0043a0002c0004t0005g0046a0002c0004t0066g0045 | 3 | HG02809.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.414-7704C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119552 | ||||||
| chr12:122119565
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-7691G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119565 | ||||||
| chr12:122119593
|
G | A | 11 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-7663G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119593 | ||||||
| chr12:122119613
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-7643G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119613 | ||||||
| chr12:122119681
|
G | A | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-7575G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119681 | ||||||
| chr12:122119686
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-7570T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119686 | ||||||
| chr12:122119690
|
G | A | 2 | a0001c0001t0033g0163a0001c0001t0033g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-7566G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119690 | ||||||
| chr12:122119892
|
TTGCCCTT others(8): Show |
T | 1 | a0002c0002t0002g0258 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.414-7363_414-7349d others(17): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122119892 | ||||||
| chr12:122120111
|
A | G | 76 | a0001c0008t0056g0217a0002c0002t0002g0197a0002c0002t0002g0198others(73): Show | 76 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.414-7145A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120111 | ||||||
| chr12:122120171
|
C | CT | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.414-7085_414-7084i others(3): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120171 | ||||||
| chr12:122120250
|
T | A | 1 | a0001c0001t0062g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.414-7006T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120250 | ||||||
| chr12:122120299
|
T | G | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-6957T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120299 | ||||||
| chr12:122120341
|
G | C | 1 | a0002c0002t0035g0271 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.414-6915G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120341 | ||||||
| chr12:122120402
|
T | C | 2 | a0002c0002t0026g0202a0002c0002t0045g0203 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.414-6854T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120402 | ||||||
| chr12:122120404
|
G | A | 20 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(17): Show | 20 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-6852G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120404 | ||||||
| chr12:122120600
|
A | G | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.414-6656A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120600 | ||||||
| chr12:122120657
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-6599A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120657 | ||||||
| chr12:122120750
|
G | A | 1 | a0002c0002t0002g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.414-6506G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120750 | ||||||
| chr12:122120778
|
T | A | 1 | a0002c0005t0009g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414-6478T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120778 | ||||||
| chr12:122120972
|
G | A | 94 | a0001c0008t0028g0014a0001c0008t0028g0016a0001c0008t0056g0217others(91): Show | 94 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.414-6284G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120972 | ||||||
| chr12:122120994
|
G | A | 3 | a0002c0010t0017g0169a0002c0010t0017g0170a0002c0010t0017g0172 | 3 | HG01891.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.414-6262G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122120994 | ||||||
| chr12:122121009
|
G | GTTTTTT | 13 | a0001c0001t0001g0126a0001c0001t0007g0346a0001c0001t0013g0034others(10): Show | 13 | HG01515.hp2 HG02083.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-6247_414-6246i others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121009 | ||||||
| chr12:122121009
|
G | GTTTTTTT | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.414-6247_414-6246i others(9): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121009 | ||||||
| chr12:122121009
|
G | GTTTTTTT others(1): Show |
27 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0110others(24): Show | 27 | HG00609.hp2 HG00735.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.414-6247_414-6246i others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121009 | ||||||
| chr12:122121010
|
G | GTTTTT | 8 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(5): Show | 8 | HG01261.hp2 HG01884.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-6232_414-6228d others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(3): Show |
1 | a0002c0002t0072g0019 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.414-6237_414-6228d others(12): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(4): Show |
2 | a0002c0002t0026g0202a0002c0002t0045g0203 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.414-6238_414-6228d others(13): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(5): Show |
3 | a0002c0010t0017g0169a0002c0010t0017g0171a0002c0010t0017g0172 | 3 | HG02615.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.414-6239_414-6228d others(14): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(6): Show |
1 | a0002c0010t0017g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.414-6240_414-6228d others(15): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(10): Show |
1 | a0002c0002t0027g0012 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.414-6244_414-6228d others(19): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(11): Show |
6 | a0002c0002t0002g0330a0002c0002t0005g0025a0002c0002t0005g0039others(3): Show | 6 | HG02615.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-6245_414-6228d others(20): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(12): Show |
3 | a0002c0002t0002g0259a0002c0002t0002g0333a0002c0004t0069g0040 | 3 | HG02040.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(21): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(13): Show |
3 | a0002c0004t0005g0042a0002c0004t0005g0044a0002c0004t0005g0046 | 3 | HG02109.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(22): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(14): Show |
4 | a0002c0002t0016g0273a0002c0004t0005g0168a0002c0004t0066g0045others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(23): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(15): Show |
12 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0002g0245others(9): Show | 12 | HG01358.hp2 HG01975.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(24): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(16): Show |
5 | a0002c0002t0002g0331a0002c0002t0010g0020a0002c0002t0042g0018others(2): Show | 5 | HG03516.hp1 HG03704.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(25): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(17): Show |
11 | a0002c0002t0002g0225a0002c0002t0002g0261a0002c0002t0002g0275others(8): Show | 11 | HG00544.hp1 HG00558.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(26): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(18): Show |
13 | a0002c0002t0002g0197a0002c0002t0002g0223a0002c0002t0002g0226others(10): Show | 13 | HG00609.hp1 HG01167.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(27): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(19): Show |
3 | a0002c0002t0002g0227a0002c0002t0002g0251a0002c0002t0002g0256 | 3 | NA18952.hp1 NA19001.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(28): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(20): Show |
2 | a0002c0002t0002g0200a0002c0002t0002g0258 | 2 | HG02523.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(29): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(21): Show |
2 | a0002c0002t0002g0222a0002c0002t0010g0017 | 2 | HG02027.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(30): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(22): Show |
2 | a0002c0002t0016g0177a0015c0013t0002g0231 | 2 | HG01109.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(31): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(23): Show |
5 | a0002c0002t0002g0224a0002c0002t0002g0229a0002c0002t0002g0250others(2): Show | 5 | HG01074.hp2 HG01433.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-6228_414-6227i others(32): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(24): Show |
2 | a0002c0002t0002g0198a0002c0004t0067g0009 | 2 | HG01081.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(33): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(25): Show |
1 | a0002c0002t0010g0023 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(34): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(27): Show |
3 | a0002c0002t0002g0252a0002c0002t0002g0277a0002c0002t0041g0266 | 3 | HG03688.hp2 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(36): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(32): Show |
1 | a0002c0002t0002g0253 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(41): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(34): Show |
1 | a0002c0002t0002g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.414-6228_414-6227i others(43): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(35): Show |
2 | a0002c0002t0002g0263a0002c0002t0002g0283 | 2 | HG04228.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.414-6228_414-6227i others(44): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(38): Show |
1 | a0002c0002t0040g0230 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(47): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(40): Show |
1 | a0002c0002t0002g0246 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(49): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | GTTTTTTT others(50): Show |
1 | a0002c0002t0002g0248 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.414-6228_414-6227i others(59): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
G | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.414-6246G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121010 | ||||||
| chr12:122121010
|
GT | G | 7 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-6228delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121010
|
GTTTT | G | 26 | a0002c0004t0003g0218a0002c0004t0003g0219a0002c0004t0004g0189others(23): Show | 26 | HG01069.hp1 HG01099.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.414-6231_414-6228d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121010 | |||||
| chr12:122121050
|
G | T | 4 | a0001c0001t0014g0067a0001c0001t0022g0074a0001c0001t0022g0161others(1): Show | 4 | HG03490.hp2 HG03831.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-6206G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121050 | ||||||
| chr12:122121140
|
G | T | 11 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(8): Show | 11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-6116G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121140 | ||||||
| chr12:122121157
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-6099A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121157 | ||||||
| chr12:122121299
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-5957T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121299 | ||||||
| chr12:122121307
|
C | CT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.414-5928dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121307 | |||||
| chr12:122121307
|
C | CTT | 13 | a0001c0001t0001g0078a0001c0001t0001g0131a0001c0001t0001g0152others(10): Show | 13 | HG00544.hp2 HG02109.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-5929_414-5928d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121307 | |||||
| chr12:122121307
|
CT | C | 8 | a0001c0003t0003g0286a0001c0003t0003g0303a0001c0003t0003g0310others(5): Show | 8 | HG01070.hp1 HG01169.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-5928delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122121307 | |||||
| chr12:122121329
|
A | T | 4 | a0002c0002t0012g0210a0002c0002t0012g0211a0002c0002t0012g0212others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-5927A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121329 | ||||||
| chr12:122121376
|
C | T | 95 | a0001c0008t0028g0014a0001c0008t0028g0016a0001c0008t0056g0217others(92): Show | 95 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.414-5880C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121376 | ||||||
| chr12:122121402
|
G | A | 58 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(55): Show | 58 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.414-5854G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121402 | ||||||
| chr12:122121464
|
C | A | 1 | a0002c0005t0009g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414-5792C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121464 | ||||||
| chr12:122121505
|
C | T | 1 | a0001c0001t0078g0129 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.414-5751C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121505 | ||||||
| chr12:122121506
|
G | A | 1 | a0002c0004t0068g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-5750G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121506 | ||||||
| chr12:122121629
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-5627A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121629 | ||||||
| chr12:122121768
|
C | A | 1 | a0002c0004t0053g0216 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.414-5488C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122121768 | ||||||
| chr12:122122049
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-5207A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122049 | ||||||
| chr12:122122050
|
C | CCTT | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-5204_414-5203i others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122122050 | |||||
| chr12:122122115
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-5141G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122115 | ||||||
| chr12:122122212
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-5044A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122212 | ||||||
| chr12:122122280
|
C | A | 1 | a0002c0002t0002g0227 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.414-4976C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122280 | ||||||
| chr12:122122290
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-4966C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122290 | ||||||
| chr12:122122340
|
C | T | 2 | a0001c0001t0033g0163a0001c0001t0033g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-4916C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122340 | ||||||
| chr12:122122368
|
G | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.414-4888G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122368 | ||||||
| chr12:122122370
|
A | T | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-4886A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122370 | ||||||
| chr12:122122514
|
C | G | 1 | a0003c0018t0061g0179 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.414-4742C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122514 | ||||||
| chr12:122122516
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.414-4740A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122516 | ||||||
| chr12:122122564
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0130 | 2 | NA18947.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.414-4692C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122564 | ||||||
| chr12:122122565
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-4691A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122565 | ||||||
| chr12:122122605
|
G | T | 11 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-4651G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122605 | ||||||
| chr12:122122614
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.414-4642T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122614 | ||||||
| chr12:122122635
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-4621A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122635 | ||||||
| chr12:122122834
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-4422A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122834 | ||||||
| chr12:122122860
|
C | CT | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.414-4383dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122122860 | |||||
| chr12:122122860
|
CT | C | 9 | a0001c0003t0003g0286a0001c0003t0003g0297a0002c0002t0002g0200others(6): Show | 9 | HG00323.hp1 HG01169.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-4383delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122122860 | |||||
| chr12:122122884
|
G | A | 2 | a0001c0008t0028g0014a0001c0008t0028g0016 | 2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.414-4372G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122884 | ||||||
| chr12:122122940
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.414-4316G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122940 | ||||||
| chr12:122122971
|
C | T | 75 | a0001c0008t0056g0217a0002c0002t0002g0197a0002c0002t0002g0198others(72): Show | 75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.414-4285C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122122971 | ||||||
| chr12:122123059
|
G | A | 2 | a0013c0021t0077g0010a0015c0013t0002g0231 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.414-4197G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123059 | ||||||
| chr12:122123169
|
T | G | 1 | a0001c0001t0006g0103 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.414-4087T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123169 | ||||||
| chr12:122123243
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0015g0145 | 2 | HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.414-4013G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123243 | ||||||
| chr12:122123282
|
C | A | 1 | a0002c0002t0038g0221 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.414-3974C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123282 | ||||||
| chr12:122123318
|
C | T | 1 | a0002c0002t0040g0230 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.414-3938C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123318 | ||||||
| chr12:122123369
|
C | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3887C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123369 | ||||||
| chr12:122123404
|
G | A | 37 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.414-3852G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123404 | ||||||
| chr12:122123420
|
C | T | 2 | a0002c0002t0012g0213a0002c0002t0012g0214 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.414-3836C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123420 | ||||||
| chr12:122123517
|
C | T | 94 | a0001c0008t0028g0014a0001c0008t0028g0016a0001c0008t0056g0217others(91): Show | 94 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.414-3739C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123517 | ||||||
| chr12:122123596
|
G | A | 11 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(8): Show | 11 | HG01993.hp1 HG02129.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-3660G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123596 | ||||||
| chr12:122123608
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3648G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123608 | ||||||
| chr12:122123662
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.414-3594G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123662 | ||||||
| chr12:122123955
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3301T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122123955 | ||||||
| chr12:122124089
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-3167A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124089 | ||||||
| chr12:122124111
|
C | A | 1 | a0002c0004t0005g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.414-3145C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124111 | ||||||
| chr12:122124173
|
C | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0082a0001c0001t0001g0123 | 3 | HG01256.hp1 HG01258.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.414-3083C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124173 | ||||||
| chr12:122124197
|
CTCAGCTG others(10): Show |
C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3058_414-3042d others(19): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124197 | ||||||
| chr12:122124203
|
T | C | 95 | a0001c0008t0028g0014a0001c0008t0028g0016a0001c0008t0056g0217others(92): Show | 95 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.414-3053T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124203 | ||||||
| chr12:122124211
|
T | TCCTCAGC others(27): Show |
1 | a0001c0008t0028g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.414-3035_414-3002d others(36): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124211 | |||||
| chr12:122124221
|
TC | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-3029delC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124221 | |||||
| chr12:122124228
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-3028A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124228 | ||||||
| chr12:122124229
|
C | T | 1 | a0002c0002t0035g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414-3027C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124229 | ||||||
| chr12:122124233
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3023C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124233 | ||||||
| chr12:122124245
|
A | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-3011A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124245 | ||||||
| chr12:122124254
|
G | GC | 39 | a0001c0001t0001g0063a0001c0001t0001g0092a0001c0001t0001g0107others(36): Show | 39 | HG00597.hp2 HG00621.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.414-2995dupC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124254 | |||||
| chr12:122124309
|
CCCCTCCT others(92): Show |
C | 1 | a0002c0002t0035g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414-2943_414-2845d others(101): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124309 | |||||
| chr12:122124326
|
CCCCACCC others(75): Show |
C | 5 | a0001c0001t0001g0084a0001c0001t0001g0107a0001c0001t0001g0131others(2): Show | 5 | HG00738.hp2 HG01934.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-2926_414-2845d others(84): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124326 | |||||
| chr12:122124330
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.414-2926A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124330 | ||||||
| chr12:122124331
|
CCCTCAGC others(9): Show |
C | 3 | a0002c0002t0002g0199a0002c0002t0016g0177a0002c0002t0016g0186 | 3 | HG01070.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.414-2909_414-2894d others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124331 | |||||
| chr12:122124331
|
CCCTCAGC others(76): Show |
C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.414-2892_414-2810d others(85): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124331 | |||||
| chr12:122124331
|
CCCTCAGC others(92): Show |
C | 1 | a0004c0007t0034g0336 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.414-2909_414-2811d others(101): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124331 | |||||
| chr12:122124359
|
CCCCGTCC others(42): Show |
C | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.414-2893_414-2845d others(51): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124359 | |||||
| chr12:122124380
|
A | ACCTCAGC others(9): Show |
1 | a0002c0002t0055g0304 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.414-2867_414-2866i others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124380 | |||||
| chr12:122124389
|
G | GC | 20 | a0001c0003t0003g0302a0001c0008t0048g0295a0002c0002t0002g0198others(17): Show | 20 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-2860dupC | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124389 | |||||
| chr12:122124413
|
C | CCACCTCA others(29): Show |
1 | a0002c0002t0002g0258 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.414-2843_414-2842i others(38): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124413 | ||||||
| chr12:122124413
|
C | G | 7 | a0001c0001t0001g0060a0001c0001t0001g0084a0001c0001t0001g0107others(4): Show | 7 | HG00738.hp2 HG01934.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-2843C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124413 | ||||||
| chr12:122124414
|
A | ACCTCAGC others(28): Show |
1 | a0002c0004t0005g0011 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.414-2811_414-2810i others(37): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124414 | |||||
| chr12:122124414
|
A | ACCTCAGC others(27): Show |
84 | a0001c0008t0028g0014a0001c0008t0028g0016a0001c0008t0056g0217others(81): Show | 84 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.414-2811_414-2810i others(36): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124414 | |||||
| chr12:122124414
|
A | ATCTCAGC others(27): Show |
8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-2842_414-2841i others(36): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124414 | ||||||
| chr12:122124414
|
A | C | 8 | a0001c0001t0001g0060a0001c0001t0001g0084a0001c0001t0001g0107others(5): Show | 8 | HG00738.hp2 HG01934.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-2842A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124414 | ||||||
| chr12:122124414
|
ACCTCAGC others(9): Show |
A | 10 | a0001c0003t0003g0306a0001c0003t0003g0307a0001c0003t0003g0322others(7): Show | 10 | HG01361.hp2 HG01496.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-2826_414-2811d others(18): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122124414 | |||||
| chr12:122124531
|
C | T | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-2725C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124531 | ||||||
| chr12:122124584
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.414-2672C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124584 | ||||||
| chr12:122124656
|
G | A | 1 | a0002c0004t0005g0007 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.414-2600G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124656 | ||||||
| chr12:122124658
|
C | T | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-2598C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124658 | ||||||
| chr12:122124736
|
T | A | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-2520T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124736 | ||||||
| chr12:122124886
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.414-2370G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124886 | ||||||
| chr12:122124957
|
A | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-2299A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122124957 | ||||||
| chr12:122125035
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.414-2221G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125035 | ||||||
| chr12:122125237
|
C | T | 7 | a0002c0002t0026g0187a0002c0002t0026g0202a0002c0002t0045g0203others(4): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-2019C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125237 | ||||||
| chr12:122125331
|
C | CA | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.414-1911dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122125331 | |||||
| chr12:122125331
|
C | CAA | 11 | a0001c0001t0001g0092a0001c0001t0007g0076a0004c0007t0019g0339others(8): Show | 11 | HG01099.hp2 HG01192.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-1912_414-1911d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122125331 | |||||
| chr12:122125331
|
CA | C | 67 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(64): Show | 67 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.414-1911delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr12 | 122125331 | |||||
| chr12:122125418
|
T | G | 1 | a0001c0003t0003g0287 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.414-1838T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125418 | ||||||
| chr12:122125442
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-1814A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125442 | ||||||
| chr12:122125472
|
C | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-1784C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125472 | ||||||
| chr12:122125567
|
A | G | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-1689A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125567 | ||||||
| chr12:122125581
|
C | T | 11 | a0002c0002t0005g0025a0002c0002t0005g0039a0002c0002t0005g0041others(8): Show | 11 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-1675C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125581 | ||||||
| chr12:122125598
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-1658C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125598 | ||||||
| chr12:122125630
|
G | A | 3 | a0001c0001t0008g0165a0001c0001t0008g0166a0001c0001t0008g0167 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.414-1626G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125630 | ||||||
| chr12:122125645
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.414-1611G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125645 | ||||||
| chr12:122125738
|
G | A | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-1518G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125738 | ||||||
| chr12:122125942
|
G | C | 1 | a0001c0003t0003g0287 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.414-1314G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122125942 | ||||||
| chr12:122126001
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.414-1255G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126001 | ||||||
| chr12:122126046
|
A | T | 75 | a0001c0008t0056g0217a0002c0002t0002g0197a0002c0002t0002g0198others(72): Show | 75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.414-1210A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126046 | ||||||
| chr12:122126059
|
C | T | 2 | a0002c0002t0021g0181a0002c0004t0021g0182 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.414-1197C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126059 | ||||||
| chr12:122126103
|
C | T | 1 | a0006c0025t0025g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1153C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126103 | ||||||
| chr12:122126104
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0155others(1): Show | 4 | HG01192.hp1 HG02698.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-1152C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126104 | ||||||
| chr12:122126105
|
A | T | 1 | a0006c0025t0025g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1151A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126105 | ||||||
| chr12:122126116
|
A | T | 1 | a0006c0025t0025g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1140A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126116 | ||||||
| chr12:122126117
|
G | C | 1 | a0006c0025t0025g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1139G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126117 | ||||||
| chr12:122126119
|
A | G | 1 | a0006c0025t0025g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1137A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126119 | ||||||
| chr12:122126136
|
C | T | 1 | a0006c0025t0025g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1120C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126136 | ||||||
| chr12:122126138
|
A | T | 1 | a0006c0025t0025g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.414-1118A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126138 | ||||||
| chr12:122126362
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-894G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126362 | ||||||
| chr12:122126376
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0082a0001c0001t0001g0123 | 3 | HG01256.hp1 HG01258.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.414-880G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126376 | ||||||
| chr12:122126457
|
A | T | 75 | a0001c0008t0056g0217a0002c0002t0002g0197a0002c0002t0002g0198others(72): Show | 75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.414-799A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126457 | ||||||
| chr12:122126552
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.414-704C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126552 | ||||||
| chr12:122126553
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-703A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126553 | ||||||
| chr12:122126603
|
G | A | 4 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-653G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126603 | ||||||
| chr12:122126653
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-603G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122126653 | ||||||
| chr12:122127053
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.414-203C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127053 | ||||||
| chr12:122127055
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-201C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127055 | ||||||
| chr12:122127073
|
A | C | 1 | a0001c0001t0015g0117 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.414-183A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127073 | ||||||
| chr12:122127073
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-183A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127073 | ||||||
| chr12:122127094
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.414-162C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127094 | ||||||
| chr12:122127138
|
G | A | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-118G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 1/16 | chr12 | 122127138 | ||||||
| chr12:122127385
|
G | A | 1 | a0001c0001t0008g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.520+23G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127385 | ||||||
| chr12:122127531
|
A | T | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+169A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127531 | ||||||
| chr12:122127599
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.520+237T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127599 | ||||||
| chr12:122127778
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.521-105G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127778 | ||||||
| chr12:122127803
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.521-80G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 2/16 | chr12 | 122127803 | ||||||
| chr12:122127981
|
G | A | 1 | a0001c0001t0033g0163 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.606+13G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122127981 | ||||||
| chr12:122128051
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.606+83T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128051 | ||||||
| chr12:122128078
|
C | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.606+110C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128078 | ||||||
| chr12:122128088
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.606+120G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128088 | ||||||
| chr12:122128201
|
T | A | 2 | a0001c0001t0011g0050a0001c0001t0011g0052 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.606+233T>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128201 | ||||||
| chr12:122128453
|
T | C | 75 | a0001c0008t0056g0217a0002c0002t0002g0197a0002c0002t0002g0198others(72): Show | 75 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.606+485T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128453 | ||||||
| chr12:122128645
|
C | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG00738.hp2 HG01106.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-492C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128645 | ||||||
| chr12:122128685
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.607-452G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128685 | ||||||
| chr12:122128693
|
C | T | 2 | a0002c0004t0024g0184a0002c0004t0024g0185 | 2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.607-444C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128693 | ||||||
| chr12:122128731
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.607-406C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128731 | ||||||
| chr12:122128765
|
C | A | 19 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(16): Show | 19 | HG00621.hp2 HG01993.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.607-372C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128765 | ||||||
| chr12:122128943
|
C | T | 1 | a0002c0002t0041g0266 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.607-194C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128943 | ||||||
| chr12:122128974
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0043g0047a0001c0001t0044g0048 | 3 | NA18982.hp2 NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.607-163T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128974 | ||||||
| chr12:122128993
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.607-144T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122128993 | ||||||
| chr12:122129006
|
T | C | 1 | a0001c0001t0043g0047 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.607-131T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122129006 | ||||||
| chr12:122129052
|
A | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.607-85A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 3/16 | chr12 | 122129052 | ||||||
| chr12:122129341
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.696+115G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129341 | ||||||
| chr12:122129346
|
G | A | 1 | a0002c0002t0005g0025 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.696+120G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129346 | ||||||
| chr12:122129396
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0015g0175 | 3 | HG01257.hp2 HG01258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.696+170C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129396 | ||||||
| chr12:122129398
|
C | T | 2 | a0002c0002t0002g0281a0002c0002t0002g0282 | 2 | NA18947.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.696+172C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129398 | ||||||
| chr12:122129417
|
C | G | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.697-171C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129417 | ||||||
| chr12:122129513
|
G | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(154): Show | 159 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.697-75G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 4/16 | chr12 | 122129513 | ||||||
| chr12:122129662
|
CT | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.738+36delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr12 | 122129662 | |||||
| chr12:122129671
|
G | C | 1 | a0002c0002t0040g0230 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.738+42G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 5/16 | chr12 | 122129671 | ||||||
| chr12:122129840
|
T | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(164): Show | 169 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.739-101T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 5/16 | chr12 | 122129840 | ||||||
| chr12:122129889
|
C | T | 6 | a0002c0004t0005g0043a0002c0004t0005g0044a0002c0004t0005g0046others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.739-52C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 5/16 | chr12 | 122129889 | ||||||
| chr12:122130218
|
G | C | 1 | a0002c0004t0054g0190 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.910+106G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130218 | ||||||
| chr12:122130223
|
G | A | 5 | a0001c0001t0018g0087a0001c0001t0018g0088a0001c0001t0018g0140others(2): Show | 5 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+111G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130223 | ||||||
| chr12:122130239
|
T | G | 4 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.910+127T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130239 | ||||||
| chr12:122130311
|
T | C | 6 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(3): Show | 6 | HG01099.hp2 HG01884.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+199T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130311 | ||||||
| chr12:122130362
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.910+250A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130362 | ||||||
| chr12:122130441
|
G | A | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.910+329G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130441 | ||||||
| chr12:122130452
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.910+340G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130452 | ||||||
| chr12:122130486
|
G | A | 70 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(67): Show | 70 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.911-358G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130486 | ||||||
| chr12:122130496
|
G | A | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.911-348G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130496 | ||||||
| chr12:122130591
|
T | C | 1 | a0001c0001t0058g0348 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.911-253T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130591 | ||||||
| chr12:122130728
|
C | A | 1 | a0002c0011t0037g0268 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.911-116C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 6/16 | chr12 | 122130728 | ||||||
| chr12:122130968
|
C | G | 211 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(208): Show | 211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1000+35C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122130968 | ||||||
| chr12:122131044
|
G | A | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1000+111G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131044 | ||||||
| chr12:122131186
|
A | G | 1 | a0002c0002t0055g0304 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1000+253A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131186 | ||||||
| chr12:122131394
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0178a0001c0001t0015g0175 | 3 | HG01257.hp2 HG01258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1000+461C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131394 | ||||||
| chr12:122131417
|
G | T | 177 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(174): Show | 177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1000+484G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131417 | ||||||
| chr12:122131441
|
C | CT | 100 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0001t0001g0130others(97): Show | 100 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1000+533dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | |||||
| chr12:122131441
|
C | CTT | 73 | a0001c0003t0003g0286a0001c0003t0003g0287a0001c0003t0003g0309others(70): Show | 73 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1000+532_1000+533d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | |||||
| chr12:122131441
|
C | CTTT | 9 | a0002c0002t0002g0247a0002c0002t0002g0252a0002c0002t0002g0254others(6): Show | 9 | HG01891.hp1 HG02027.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1000+531_1000+533d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | |||||
| chr12:122131441
|
C | CTTTTT | 7 | a0002c0002t0010g0020a0002c0002t0010g0021a0002c0002t0010g0022others(4): Show | 7 | HG00621.hp2 HG03704.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000+529_1000+533d others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | |||||
| chr12:122131441
|
CT | C | 19 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0001g0123others(16): Show | 19 | HG01168.hp2 HG01256.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1000+533delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131441 | |||||
| chr12:122131552
|
C | T | 178 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(175): Show | 178 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.1000+619C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131552 | ||||||
| chr12:122131693
|
T | C | 89 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1001-599T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131693 | ||||||
| chr12:122131739
|
G | A | 177 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(174): Show | 177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1001-553G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131739 | ||||||
| chr12:122131816
|
C | T | 4 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-476C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122131816 | ||||||
| chr12:122131912
|
C | CT | 21 | a0001c0001t0001g0070a0001c0001t0001g0106a0001c0001t0001g0149others(18): Show | 21 | HG00140.hp1 HG00621.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-351dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122131912
|
CT | C | 21 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0081others(18): Show | 21 | HG01168.hp1 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-351delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122131912
|
CTT | C | 18 | a0001c0001t0001g0138a0001c0001t0033g0163a0002c0002t0005g0025others(15): Show | 18 | HG01256.hp2 HG01993.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1001-352_1001-351d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122131912
|
CTTT | C | 14 | a0001c0003t0003g0286a0001c0003t0003g0287a0001c0003t0003g0302others(11): Show | 14 | HG00673.hp1 HG00741.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1001-353_1001-351d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122131912
|
CTTTT | C | 84 | a0001c0003t0003g0004a0001c0003t0003g0288a0001c0003t0003g0290others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1001-354_1001-351d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122131912
|
CTTTTT | C | 79 | a0001c0003t0003g0328a0001c0008t0028g0014a0001c0008t0028g0016others(76): Show | 79 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1001-355_1001-351d others(7): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122131912
|
CTTTTTTT others(1): Show |
C | 6 | a0004c0007t0034g0335a0004c0007t0034g0336a0004c0007t0075g0338others(3): Show | 6 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001-358_1001-351d others(10): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122131912
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001-359_1001-351d others(11): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122131912
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0010g0017 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1001-365_1001-351d others(17): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr12 | 122131912 | |||||
| chr12:122132211
|
C | A | 1 | a0002c0004t0004g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1001-81C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122132211 | ||||||
| chr12:122132212
|
G | A | 178 | a0001c0001t0058g0348a0001c0003t0003g0004a0001c0003t0003g0286others(175): Show | 178 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.1001-80G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122132212 | ||||||
| chr12:122132219
|
G | A | 178 | a0001c0001t0058g0348a0001c0003t0003g0004a0001c0003t0003g0286others(175): Show | 178 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.1001-73G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 7/16 | chr12 | 122132219 | ||||||
| chr12:122132411
|
G | A | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1092+28G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132411 | ||||||
| chr12:122132729
|
C | T | 8 | a0002c0002t0010g0017a0002c0002t0010g0020a0002c0002t0010g0021others(5): Show | 8 | HG00621.hp2 HG02027.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.1092+346C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132729 | ||||||
| chr12:122132768
|
TG | T | 177 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(174): Show | 177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1092+389delG | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr12 | 122132768 | |||||
| chr12:122132843
|
A | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1092+460A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132843 | ||||||
| chr12:122132871
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1093-477C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132871 | ||||||
| chr12:122132987
|
C | T | 1 | a0001c0001t0022g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1093-361C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122132987 | ||||||
| chr12:122133011
|
C | G | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093-337C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 8/16 | chr12 | 122133011 | ||||||
| chr12:122134025
|
C | T | 1 | a0001c0001t0008g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1732+38C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134025 | ||||||
| chr12:122134205
|
G | GT | 96 | a0001c0001t0001g0158a0001c0001t0001g0188a0001c0001t0007g0083others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1732+231dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134205 | |||||
| chr12:122134205
|
G | GTT | 36 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(33): Show | 36 | HG01099.hp2 HG01123.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1732+230_1732+231d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134205 | |||||
| chr12:122134205
|
G | GTTT | 17 | a0002c0002t0005g0025a0002c0002t0005g0041a0002c0004t0005g0005others(14): Show | 17 | HG01243.hp2 HG01993.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1732+229_1732+231d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134205 | |||||
| chr12:122134264
|
G | A | 7 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1732+277G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134264 | ||||||
| chr12:122134277
|
C | T | 1 | a0001c0001t0044g0048 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1732+290C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134277 | ||||||
| chr12:122134304
|
CCTT | C | 3 | a0002c0002t0026g0187a0002c0002t0026g0202a0002c0002t0045g0203 | 3 | HG02109.hp1 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1732+319_1732+321d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134304 | |||||
| chr12:122134419
|
T | C | 177 | a0001c0001t0015g0143a0001c0003t0003g0004a0001c0003t0003g0286others(174): Show | 177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1732+432T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134419 | ||||||
| chr12:122134428
|
G | A | 2 | a0002c0004t0003g0218a0002c0004t0003g0219 | 2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1732+441G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134428 | ||||||
| chr12:122134445
|
C | CA | 176 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(173): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1732+460dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134445 | |||||
| chr12:122134677
|
C | CT | 93 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(90): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1733-533dupT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134677 | |||||
| chr12:122134677
|
CT | C | 22 | a0001c0001t0001g0079a0001c0001t0008g0165a0001c0001t0032g0105others(19): Show | 22 | HG01069.hp2 HG01243.hp2 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.1733-533delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134677 | |||||
| chr12:122134714
|
G | T | 176 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(173): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1733-510G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134714 | ||||||
| chr12:122134767
|
C | T | 4 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0027g0012others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1733-457C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134767 | ||||||
| chr12:122134850
|
C | T | 204 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(201): Show | 204 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1733-374C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134850 | ||||||
| chr12:122134939
|
G | T | 3 | a0001c0003t0003g0318a0001c0003t0003g0319a0001c0003t0003g0320 | 3 | HG00741.hp2 HG01943.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1733-285G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122134939 | ||||||
| chr12:122134981
|
CT | C | 176 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(173): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1733-235delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr12 | 122134981 | |||||
| chr12:122135159
|
C | T | 9 | a0004c0007t0019g0339a0004c0007t0034g0335a0004c0007t0034g0336others(6): Show | 9 | HG01099.hp2 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1733-65C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 9/16 | chr12 | 122135159 | ||||||
| chr12:122135683
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2032+17C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135683 | ||||||
| chr12:122135700
|
C | T | 1 | a0002c0009t0070g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2032+34C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135700 | ||||||
| chr12:122135816
|
C | T | 1 | a0002c0004t0068g0173 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2032+150C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135816 | ||||||
| chr12:122135834
|
G | T | 1 | a0002c0002t0002g0199 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2032+168G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135834 | ||||||
| chr12:122135919
|
C | T | 1 | a0002c0002t0002g0200 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2032+253C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122135919 | ||||||
| chr12:122136142
|
A | G | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2032+476A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136142 | ||||||
| chr12:122136178
|
A | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 5 | HG02683.hp2 HG02738.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.2032+512A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136178 | ||||||
| chr12:122136217
|
G | A | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2032+551G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136217 | ||||||
| chr12:122136387
|
T | TA | 6 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG00738.hp2 HG01106.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.2032+721_2032+722i others(3): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136387 | ||||||
| chr12:122136411
|
G | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2032+745G>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136411 | ||||||
| chr12:122136457
|
TGC | T | 9 | a0001c0008t0028g0016a0001c0008t0056g0217a0002c0002t0012g0210others(6): Show | 9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2032+792_2032+793d others(4): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136457 | ||||||
| chr12:122136457
|
TGCA | T | 4 | a0001c0003t0003g0315a0001c0003t0003g0320a0002c0004t0004g0195others(1): Show | 4 | HG00741.hp2 HG03579.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2032+792_2032+794d others(5): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136457 | ||||||
| chr12:122136457
|
TGCAA | T | 81 | a0001c0003t0003g0004a0001c0003t0003g0287a0001c0003t0003g0288others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.2032+792_2032+795d others(6): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136457 | ||||||
| chr12:122136458
|
G | A | 80 | a0001c0008t0028g0014a0002c0002t0002g0197a0002c0002t0002g0198others(77): Show | 80 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2032+792G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136458 | ||||||
| chr12:122136459
|
C | CA | 28 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0121others(25): Show | 29 | HG00544.hp2 HG01168.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2032+816dupA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 122136459 | |||||
| chr12:122136459
|
C | CAAAAAA | 22 | a0002c0002t0005g0039a0002c0002t0005g0041a0002c0004t0005g0005others(19): Show | 22 | HG01099.hp2 HG01884.hp2 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.2032+811_2032+816d others(8): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 122136459 | |||||
| chr12:122136459
|
CA | C | 18 | a0001c0001t0001g0109a0001c0001t0015g0143a0001c0001t0033g0163others(15): Show | 18 | HG00621.hp2 HG02027.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2032+816delA | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr12 | 122136459 | |||||
| chr12:122136461
|
A | C | 9 | a0001c0008t0028g0016a0001c0008t0056g0217a0002c0002t0012g0210others(6): Show | 9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2032+795A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136461 | ||||||
| chr12:122136461
|
A | T | 1 | a0009c0015t0003g0096 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2032+795A>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136461 | ||||||
| chr12:122136462
|
A | C | 4 | a0001c0003t0003g0315a0001c0003t0003g0320a0002c0004t0004g0195others(1): Show | 4 | HG00741.hp2 HG03579.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2032+796A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136462 | ||||||
| chr12:122136463
|
A | C | 82 | a0001c0003t0003g0004a0001c0003t0003g0287a0001c0003t0003g0288others(79): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.2032+797A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136463 | ||||||
| chr12:122136464
|
A | C | 1 | a0001c0003t0003g0286 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2032+798A>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136464 | ||||||
| chr12:122136534
|
T | C | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2032+868T>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136534 | ||||||
| chr12:122136841
|
G | A | 13 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(10): Show | 13 | HG00621.hp2 HG02027.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.2033-628G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136841 | ||||||
| chr12:122136868
|
C | T | 1 | a0015c0013t0002g0231 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2033-601C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122136868 | ||||||
| chr12:122137116
|
A | G | 4 | a0002c0004t0005g0043a0002c0004t0005g0046a0002c0004t0066g0045others(1): Show | 4 | HG02717.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2033-353A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137116 | ||||||
| chr12:122137145
|
T | G | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2033-324T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137145 | ||||||
| chr12:122137187
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2033-282C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137187 | ||||||
| chr12:122137217
|
T | G | 1 | a0009c0015t0003g0096 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2033-252T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137217 | ||||||
| chr12:122137219
|
G | A | 1 | a0009c0015t0003g0096 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2033-250G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137219 | ||||||
| chr12:122137441
|
G | A | 6 | a0001c0008t0056g0217a0002c0002t0012g0210a0002c0002t0012g0211others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2033-28G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137441 | ||||||
| chr12:122137444
|
C | A | 1 | a0009c0015t0003g0096 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2033-25C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 11/16 | chr12 | 122137444 | ||||||
| chr12:122137660
|
CT | C | 179 | a0001c0001t0033g0163a0001c0001t0033g0164a0001c0003t0003g0004others(176): Show | 179 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.2154+72delT | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr12 | 122137660 | |||||
| chr12:122137675
|
G | A | 2 | a0001c0001t0033g0163a0001c0001t0033g0164 | 2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2154+85G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | chr12 | 122137675 | ||||||
| chr12:122137836
|
G | A | 1 | a0002c0002t0021g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2154+246G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | chr12 | 122137836 | ||||||
| chr12:122137968
|
C | G | 1 | a0002c0002t0026g0202 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2155-226C>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | chr12 | 122137968 | ||||||
| chr12:122138090
|
C | T | 1 | a0002c0002t0002g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2155-104C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 12/16 | chr12 | 122138090 | ||||||
| chr12:122138620
|
T | TGG | 13 | a0001c0008t0028g0014a0001c0008t0028g0016a0002c0002t0010g0017others(10): Show | 13 | HG00621.hp2 HG02027.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.2384+71_2384+72dup others(2): Show |
MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr12 | 122138620 | |||||
| chr12:122138735
|
G | A | 1 | a0001c0001t0015g0117 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2385-80G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 14/16 | chr12 | 122138735 | ||||||
| chr12:122139008
|
T | G | 1 | a0002c0002t0002g0270 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2508+70T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139008 | ||||||
| chr12:122139048
|
A | G | 89 | a0001c0008t0028g0014a0001c0008t0028g0016a0001c0008t0056g0217others(86): Show | 89 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.2508+110A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139048 | ||||||
| chr12:122139076
|
C | T | 1 | a0007c0014t0019g0340 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2508+138C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139076 | ||||||
| chr12:122139387
|
A | G | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2508+449A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139387 | ||||||
| chr12:122139451
|
G | A | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2508+513G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139451 | ||||||
| chr12:122139505
|
G | C | 1 | a0012c0022t0023g0265 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2508+567G>C | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139505 | ||||||
| chr12:122139617
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2508+679C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139617 | ||||||
| chr12:122139657
|
A | G | 2 | a0005c0012t0073g0160a0005c0012t0074g0159 | 2 | HG02895.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2508+719A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139657 | ||||||
| chr12:122139705
|
C | T | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2508+767C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139705 | ||||||
| chr12:122139803
|
G | A | 176 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(173): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2508+865G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139803 | ||||||
| chr12:122139834
|
C | T | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2508+896C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122139834 | ||||||
| chr12:122140009
|
A | G | 1 | a0001c0001t0029g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2509-945A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140009 | ||||||
| chr12:122140087
|
G | A | 1 | a0001c0003t0003g0313 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2509-867G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140087 | ||||||
| chr12:122140462
|
A | G | 1 | a0001c0001t0013g0349 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2509-492A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140462 | ||||||
| chr12:122140550
|
C | T | 176 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(173): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2509-404C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140550 | ||||||
| chr12:122140584
|
G | A | 33 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(30): Show | 33 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.2509-370G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140584 | ||||||
| chr12:122140662
|
C | T | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2509-292C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140662 | ||||||
| chr12:122140665
|
A | G | 209 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(206): Show | 209 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2509-289A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140665 | ||||||
| chr12:122140895
|
C | T | 1 | a0002c0002t0002g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2509-59C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140895 | ||||||
| chr12:122140921
|
C | T | 1 | a0001c0001t0007g0346 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2509-33C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 15/16 | chr12 | 122140921 | ||||||
| chr12:122141199
|
C | A | 4 | a0002c0005t0009g0235a0002c0005t0009g0237a0002c0005t0009g0238others(1): Show | 4 | HG01109.hp1 HG01934.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.2638+116C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141199 | ||||||
| chr12:122141208
|
A | G | 71 | a0002c0002t0002g0197a0002c0002t0002g0198a0002c0002t0002g0199others(68): Show | 71 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2638+125A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141208 | ||||||
| chr12:122141227
|
T | G | 176 | a0001c0003t0003g0004a0001c0003t0003g0286a0001c0003t0003g0287others(173): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2638+144T>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141227 | ||||||
| chr12:122141417
|
G | A | 6 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2639-274G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141417 | ||||||
| chr12:122141445
|
A | G | 209 | a0001c0001t0013g0034a0001c0001t0013g0035a0001c0001t0013g0036others(206): Show | 209 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2639-246A>G | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141445 | ||||||
| chr12:122141480
|
G | A | 1 | a0013c0021t0077g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2639-211G>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141480 | ||||||
| chr12:122141503
|
C | A | 2 | a0002c0002t0021g0181a0002c0004t0021g0182 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2639-188C>A | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141503 | ||||||
| chr12:122141568
|
C | T | 3 | a0001c0001t0033g0163a0001c0001t0033g0164a0002c0009t0070g0033 | 3 | HG02055.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2639-123C>T | MLXIP | ENSG00000175727.15 | transcript | ENST00000319080.12 | protein_coding | 16/16 | chr12 | 122141568 |