Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 11043 |
|---|---|
| ensemblid | ENSG00000080561.14 |
| hgncid | 7096 |
| symbol | MID2 |
| name | midline 2 |
| refseq_nuc | NM_012216.4 |
| refseq_prot | NP_036348.2 |
| ensembl_nuc | ENST00000262843.11 |
| ensembl_prot | ENSP00000262843.6 |
| mane_status | MANE Select |
| chr | chrX |
| start | 107825866 |
| end | 107931637 |
| strand | + |
| ver | v1.2 |
| region | chrX:107825866-107931637 |
| region5000 | chrX:107820866-107936637 |
| regionname0 | MID2_chrX_107825866_107931637 |
| regionname5000 | MID2_chrX_107820866_107936637 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 735 | 170 | 63 | 22 | 61 | 5 | 17 | 45 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0002 | 0/0 | 735 | 8 | 0 | 2 | 1 | 2 | 3 | 1 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0003 | 0/0 | 383 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0004 | 0/0 | 481 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0005 | 0/0 | 320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2208 | 141 | 53 | 21 | 47 | 4 | 14 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| c0002 | 0/0 | 2208 | 28 | 10 | 1 | 14 | 1 | 2 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| c0003 | 0/0 | 2208 | 8 | 0 | 2 | 1 | 2 | 3 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| c0004 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| c0005 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| c0006 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| c0007 | 0/0 | 2207 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 5126 | 96 | 26 | 16 | 34 | 4 | 14 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0002 | 0/0 | 5126 | 41 | 5 | 5 | 22 | 3 | 6 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0003 | 0/0 | 5126 | 9 | 8 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0004 | 0/0 | 5126 | 7 | 0 | 0 | 7 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0005 | 0/0 | 5126 | 7 | 7 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0006 | 0/0 | 5126 | 5 | 4 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0007 | 0/0 | 5126 | 5 | 4 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0008 | 0/0 | 5126 | 3 | 3 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0009 | 0/0 | 5126 | 2 | 2 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0010 | 0/0 | 5126 | 2 | 2 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0011 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0012 | 0/0 | 5126 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0013 | 0/0 | 5126 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| t0014 | 0/0 | 5126 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2208 | 141 | 53 | 21 | 47 | 4 | 14 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0002 | 0/0 | 2208 | 28 | 10 | 1 | 14 | 1 | 2 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0006 | 0/0 | 2208 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0002c0003 | 0/0 | 2208 | 8 | 0 | 2 | 1 | 2 | 3 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0003c0007 | 0/0 | 2207 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0004c0004 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0005c0005 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7333 | 87 | 20 | 16 | 31 | 4 | 14 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0002 | 0/0 | 7333 | 13 | 4 | 1 | 8 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0003 | 0/0 | 7333 | 9 | 8 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0004 | 0/0 | 7333 | 7 | 0 | 0 | 7 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0005 | 0/0 | 7333 | 7 | 7 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0006 | 0/0 | 7333 | 3 | 2 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0007 | 0/0 | 7333 | 5 | 4 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0008 | 0/0 | 7333 | 3 | 3 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0009 | 0/0 | 7333 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0010 | 0/0 | 7333 | 2 | 2 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0011 | 0/0 | 7333 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0012 | 0/0 | 7333 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0013 | 0/0 | 7333 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0001t0014 | 0/0 | 7333 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0002t0001 | 0/0 | 7333 | 7 | 6 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0002t0002 | 0/0 | 7333 | 18 | 1 | 1 | 13 | 1 | 2 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0002t0006 | 0/0 | 7333 | 2 | 2 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0002t0009 | 0/0 | 7333 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0001c0006t0002 | 0/0 | 7333 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0002c0003t0002 | 0/0 | 7333 | 8 | 0 | 2 | 1 | 2 | 3 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0003c0007t0002 | 0/0 | 7332 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0004c0004t0001 | 0/0 | 7334 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| a0005c0005t0001 | 0/0 | 7334 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | copy fasta | chrX | 107820866 | 107936637 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0012g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0013g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0001t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0002t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0001c0006t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0002c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0003c0007t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0004c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| a0005c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00735 | hp2 | a0002 | c0003 | t0002 | g0161 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0173 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0167 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0142 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01168 | hp2 | a0003 | c0007 | t0002 | g0131 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01255 | hp1 | a0002 | c0003 | t0002 | g0162 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01515 | hp1 | a0002 | c0003 | t0002 | g0160 | EUR | IBS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01516 | hp2 | a0002 | c0003 | t0002 | g0138 | EUR | IBS | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0168 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | CDX | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0180 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02738 | hp1 | a0001 | c0006 | t0002 | g0128 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0171 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0139 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0166 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0025 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | ESN | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03225 | hp1 | a0001 | c0002 | t0006 | g0179 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0130 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03704 | hp2 | a0002 | c0003 | t0002 | g0159 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03710 | hp1 | a0002 | c0003 | t0002 | g0163 | SAS | PJL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0164 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18975 | hp2 | a0001 | c0001 | t0013 | g0114 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0123 | AFR | LWK | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19062 | hp1 | a0004 | c0004 | t0001 | g0110 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19090 | hp1 | a0002 | c0003 | t0002 | g0170 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19091 | hp1 | a0005 | c0005 | t0001 | g0103 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0127 | EUR | TSI | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0133 | AFR | ACB | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | USA | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | USA | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | USA | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA21309 | hp1 | a0001 | c0002 | t0009 | g0176 | AFR | LWK | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0100 | REF | REF | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0067 | REF | REF | MID2_chrX_107820866_107936637 | MID2 | chrX | 107820866 | 107936637 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:107905499
|
G | GC | 1 | a0005 | 1 | NA19091.hp1 | frameshift_variant | HIGH | c.947dupC | p.Gln317fs | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/10 | 1509/7333 | 948/2208 | 316/735 | INFO_REALIGN_3_PRIME | chrX | 107905499 | |
| chrX:107916047
|
CA | C | 1 | a0003 | 1 | HG01168.hp2 | frameshift_variant | HIGH | c.1121delA | p.Asn374fs | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/10 | 1682/7333 | 1121/2208 | 374/735 | INFO_REALIGN_3_PRIME | chrX | 107916047 | |
| chrX:107916061
|
C | A | 2 | a0002a0003 | 9 | HG00735.hp2 HG01168.hp2 HG01255.hp1 others(6): Show |
missense_variant | MODERATE | c.1133C>A | p.Ala378Asp | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/10 | 1694/7333 | 1133/2208 | 378/735 | chrX | 107916061 | ||
| chrX:107917726
|
C | CG | 1 | a0004 | 1 | NA19062.hp1 | frameshift_variant | HIGH | c.1426dupG | p.Ala476fs | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/10 | 1988/7333 | 1427/2208 | 476/735 | INFO_REALIGN_3_PRIME | chrX | 107917726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:107840845
|
A | C | 3 | a0001c0002a0001c0006a0003c0007 | 30 | HG01168.hp1 HG01168.hp2 HG01891.hp1 others(27): Show |
synonymous_variant | LOW | c.180A>C | p.Ser60Ser | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/10 | 741/7333 | 180/2208 | 60/735 | chrX | 107840845 | ||
| chrX:107917732
|
G | A | 1 | a0001c0006 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1428G>A | p.Ala476Ala | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/10 | 1989/7333 | 1428/2208 | 476/735 | chrX | 107917732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:107826162
|
T | C | 1 | a0001c0001t0011 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-265T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/10 | 265 | chrX | 107826162 | |||||
| chrX:107927287
|
T | G | 1 | a0001c0001t0008 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*214T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 214 | chrX | 107927287 | |||||
| chrX:107927666
|
T | G | 1 | a0001c0001t0003 | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*593T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 593 | chrX | 107927666 | |||||
| chrX:107927867
|
C | T | 1 | a0001c0001t0014 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 794 | chrX | 107927867 | |||||
| chrX:107928325
|
C | G | 1 | a0001c0001t0005 | 7 | HG02922.hp1 HG02965.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1252C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1252 | chrX | 107928325 | |||||
| chrX:107928414
|
T | A | 3 | a0001c0001t0005a0001c0001t0009a0001c0002t0009 | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1341T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1341 | chrX | 107928414 | |||||
| chrX:107928415
|
A | T | 1 | a0001c0001t0013 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1342A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1342 | chrX | 107928415 | |||||
| chrX:107928744
|
A | C | 2 | a0001c0001t0007a0001c0001t0011 | 6 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1671A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1671 | chrX | 107928744 | |||||
| chrX:107929008
|
C | T | 1 | a0001c0001t0012 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1935C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 1935 | chrX | 107929008 | |||||
| chrX:107929811
|
C | A | 1 | a0001c0001t0007 | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2738C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 2738 | chrX | 107929811 | |||||
| chrX:107930293
|
T | C | 2 | a0001c0001t0006a0001c0002t0006 | 5 | HG01243.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3220T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 3220 | chrX | 107930293 | |||||
| chrX:107930939
|
T | A | 10 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(7): Show | 49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3866T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 3866 | chrX | 107930939 | |||||
| chrX:107931519
|
T | C | 1 | a0001c0001t0004 | 7 | NA18966.hp1 NA18973.hp2 NA18983.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4446T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 4446 | chrX | 107931519 | |||||
| chrX:107931625
|
A | G | 1 | a0001c0001t0010 | 2 | HG02486.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4552A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 10/10 | 4552 | chrX | 107931625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:107826534
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4+104G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826534 | ||||||
| chrX:107826545
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4+115G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826545 | ||||||
| chrX:107826763
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(1): Show | 4 | HG02145.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4+333G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826763 | ||||||
| chrX:107826883
|
C | A | 1 | a0001c0001t0002g0006 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4+453C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826883 | ||||||
| chrX:107826977
|
A | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(55): Show | 58 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.4+547A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107826977 | ||||||
| chrX:107827792
|
T | A | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02630.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4+1362T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107827792 | ||||||
| chrX:107827938
|
C | T | 2 | a0001c0002t0006g0179a0001c0002t0006g0180 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4+1508C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107827938 | ||||||
| chrX:107828280
|
CTCTTT | C | 13 | a0001c0001t0002g0021a0001c0001t0005g0016a0001c0001t0005g0017others(10): Show | 13 | HG01243.hp1 HG02818.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.4+1866_4+1870delTC others(3): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828280 | |||||
| chrX:107828310
|
C | CT | 10 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG02165.hp1 HG02622.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4+1899dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | |||||
| chrX:107828310
|
C | CTT | 24 | a0001c0001t0003g0126a0001c0001t0007g0139a0001c0002t0001g0146others(21): Show | 24 | HG01109.hp1 HG01168.hp1 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.4+1898_4+1899dupTT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | |||||
| chrX:107828310
|
C | CTTT | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG00735.hp2 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.4+1897_4+1899dupTT others(1): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | |||||
| chrX:107828310
|
C | CTTTT | 10 | a0001c0001t0002g0178a0001c0001t0003g0007a0001c0001t0003g0008others(7): Show | 10 | HG00741.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.4+1896_4+1899dupTT others(2): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | |||||
| chrX:107828310
|
C | CTTTTT | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4+1895_4+1899dupTT others(3): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | |||||
| chrX:107828310
|
CT | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG00621.hp1 HG02165.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.4+1899delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | |||||
| chrX:107828310
|
CTTT | C | 3 | a0001c0001t0002g0132a0001c0001t0008g0134a0001c0001t0010g0133 | 3 | HG01891.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4+1897_4+1899delTT others(1): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828310 | |||||
| chrX:107828312
|
T | TTC | 5 | a0001c0002t0002g0127a0001c0002t0002g0129a0001c0002t0002g0130others(2): Show | 5 | HG01168.hp2 HG02738.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.4+1883_4+1884insCT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107828312 | |||||
| chrX:107828331
|
A | G | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4+1901A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107828331 | ||||||
| chrX:107828440
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4+2010T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107828440 | ||||||
| chrX:107828480
|
T | A | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02622.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4+2050T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107828480 | ||||||
| chrX:107828902
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4+2472C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107828902 | ||||||
| chrX:107829196
|
G | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.4+2766G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829196 | ||||||
| chrX:107829243
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.4+2813C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829243 | ||||||
| chrX:107829578
|
G | C | 12 | a0001c0001t0002g0021a0001c0001t0005g0016a0001c0001t0005g0017others(9): Show | 12 | HG01243.hp1 HG02886.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.4+3148G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829578 | ||||||
| chrX:107829805
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4+3375G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829805 | ||||||
| chrX:107829818
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(82): Show |
intron_variant | MODIFIER | c.4+3388C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107829818 | ||||||
| chrX:107830226
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4+3796C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107830226 | ||||||
| chrX:107830607
|
G | A | 7 | a0002c0003t0002g0138a0002c0003t0002g0159a0002c0003t0002g0160others(4): Show | 7 | HG00735.hp2 HG01255.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.4+4177G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107830607 | ||||||
| chrX:107830801
|
T | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02622.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4+4371T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107830801 | ||||||
| chrX:107831244
|
T | C | 2 | a0001c0001t0003g0177a0001c0001t0009g0026 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4+4814T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107831244 | ||||||
| chrX:107831270
|
G | A | 10 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(7): Show | 10 | HG01109.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.4+4840G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107831270 | ||||||
| chrX:107832962
|
G | A | 1 | a0001c0001t0005g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4+6532G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107832962 | ||||||
| chrX:107832992
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4+6562A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107832992 | ||||||
| chrX:107833201
|
G | A | 3 | a0001c0001t0002g0132a0001c0001t0008g0134a0001c0001t0010g0133 | 3 | HG01891.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4+6771G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833201 | ||||||
| chrX:107833411
|
T | TTA | 7 | a0001c0001t0001g0040a0001c0001t0003g0011a0001c0001t0003g0012others(4): Show | 7 | HG01109.hp1 HG02015.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4+6999_4+7000dupAT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833411 | |||||
| chrX:107833411
|
T | TTATA | 9 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(6): Show | 9 | HG02622.hp2 HG02723.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.4+6997_4+7000dupAT others(2): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833411 | |||||
| chrX:107833425
|
A | AT | 1 | a0001c0002t0009g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4+6996dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833425 | |||||
| chrX:107833425
|
A | T | 1 | a0002c0003t0002g0138 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4+6995A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833425 | ||||||
| chrX:107833427
|
A | AT | 24 | a0001c0001t0003g0177a0001c0001t0009g0026a0001c0002t0001g0146others(21): Show | 24 | HG01168.hp1 HG01168.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.4+6998dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833427 | |||||
| chrX:107833427
|
A | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(17): Show | 20 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.4+6997A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833427 | ||||||
| chrX:107833428
|
TA | T | 3 | a0001c0001t0002g0132a0001c0001t0008g0134a0001c0001t0010g0133 | 3 | HG01891.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4+6999delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833428 | ||||||
| chrX:107833429
|
A | AT | 6 | a0001c0001t0001g0165a0001c0001t0007g0139a0001c0001t0007g0166others(3): Show | 6 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4+7007dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107833429 | |||||
| chrX:107833429
|
A | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00558.hp2 HG00673.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.4+6999A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833429 | ||||||
| chrX:107833431
|
T | A | 28 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(25): Show | 28 | HG01109.hp1 HG01243.hp1 HG02622.hp1 others(25): Show |
intron_variant | MODIFIER | c.4+7001T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833431 | ||||||
| chrX:107833437
|
T | A | 1 | a0001c0001t0002g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4+7007T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833437 | ||||||
| chrX:107833577
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18988.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.5-7093G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107833577 | ||||||
| chrX:107834036
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5-6634T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834036 | ||||||
| chrX:107834086
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0043 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.5-6584G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834086 | ||||||
| chrX:107834234
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.5-6436A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834234 | ||||||
| chrX:107834554
|
G | A | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5-6116G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834554 | ||||||
| chrX:107834740
|
G | C | 1 | a0001c0002t0001g0154 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5-5930G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834740 | ||||||
| chrX:107834958
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02630.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.5-5712C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107834958 | ||||||
| chrX:107835201
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.5-5469T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107835201 | ||||||
| chrX:107835421
|
C | T | 2 | a0001c0001t0008g0013a0001c0001t0008g0014 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.5-5249C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107835421 | ||||||
| chrX:107835518
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0012g0173 | 2 | HG00741.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5-5152C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107835518 | ||||||
| chrX:107835654
|
A | ATCT | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(77): Show | 80 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.5-5014_5-5012dupCT others(1): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107835654 | |||||
| chrX:107836260
|
C | CT | 1 | a0001c0001t0001g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5-4397dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107836260 | |||||
| chrX:107836400
|
T | C | 10 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(7): Show | 10 | HG01109.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.5-4270T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836400 | ||||||
| chrX:107836493
|
C | T | 2 | a0001c0002t0006g0179a0001c0002t0006g0180 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.5-4177C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836493 | ||||||
| chrX:107836516
|
G | A | 1 | a0001c0002t0002g0140 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5-4154G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836516 | ||||||
| chrX:107836530
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5-4140C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836530 | ||||||
| chrX:107836542
|
C | T | 7 | a0001c0001t0001g0165a0001c0001t0007g0139a0001c0001t0007g0166others(4): Show | 7 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.5-4128C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107836542 | ||||||
| chrX:107836553
|
C | CT | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.5-4103dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107836553 | |||||
| chrX:107836553
|
CT | C | 11 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 11 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.5-4103delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107836553 | |||||
| chrX:107836553
|
CTT | C | 1 | a0001c0001t0014g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5-4104_5-4103delTT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107836553 | |||||
| chrX:107837299
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.5-3371G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107837299 | ||||||
| chrX:107837538
|
T | TA | 3 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0002g0046 | 3 | HG02622.hp1 HG03041.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.5-3120dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107837538 | |||||
| chrX:107837538
|
TA | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(54): Show | 57 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.5-3120delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107837538 | |||||
| chrX:107837539
|
A | T | 3 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0109 | 3 | NA18966.hp1 NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.5-3131A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107837539 | ||||||
| chrX:107837597
|
CA | C | 4 | a0001c0001t0001g0106a0001c0001t0003g0015a0001c0001t0008g0013others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.5-3059delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107837597 | |||||
| chrX:107837857
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5-2813T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107837857 | ||||||
| chrX:107838520
|
A | G | 2 | a0001c0001t0002g0178a0001c0001t0012g0173 | 2 | HG00741.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.5-2150A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838520 | ||||||
| chrX:107838600
|
GTAGT | G | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.5-2064_5-2061delAG others(2): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107838600 | |||||
| chrX:107838787
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(82): Show |
intron_variant | MODIFIER | c.5-1883A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838787 | ||||||
| chrX:107838874
|
T | C | 7 | a0001c0001t0002g0021a0001c0001t0005g0016a0001c0001t0005g0017others(4): Show | 7 | HG02922.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5-1796T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838874 | ||||||
| chrX:107838962
|
T | C | 10 | a0001c0001t0002g0178a0001c0001t0012g0173a0002c0003t0002g0138others(7): Show | 10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.5-1708T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838962 | ||||||
| chrX:107838984
|
C | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(55): Show | 58 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.5-1686C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107838984 | ||||||
| chrX:107839370
|
G | GT | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5-1296dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107839370 | |||||
| chrX:107839375
|
G | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5-1295G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839375 | ||||||
| chrX:107839379
|
G | GT | 14 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0165others(11): Show | 14 | HG01099.hp1 HG01106.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.5-1277dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107839379 | |||||
| chrX:107839379
|
G | GTT | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.5-1278_5-1277dupTT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107839379 | |||||
| chrX:107839379
|
G | GTTT | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5-1279_5-1277dupTT others(1): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107839379 | |||||
| chrX:107839379
|
G | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5-1291G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839379 | ||||||
| chrX:107839434
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5-1236T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839434 | ||||||
| chrX:107839478
|
A | T | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(55): Show | 58 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.5-1192A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839478 | ||||||
| chrX:107839734
|
A | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 68 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.5-936A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107839734 | ||||||
| chrX:107840042
|
A | G | 11 | a0001c0001t0002g0021a0001c0001t0005g0016a0001c0001t0005g0017others(8): Show | 11 | HG01243.hp1 HG02886.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.5-628A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107840042 | ||||||
| chrX:107840243
|
CAT | C | 10 | a0001c0001t0002g0178a0001c0001t0012g0173a0002c0003t0002g0138others(7): Show | 10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.5-425_5-424delTA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chrX | 107840243 | |||||
| chrX:107840332
|
A | T | 8 | a0002c0003t0002g0138a0002c0003t0002g0159a0002c0003t0002g0160others(5): Show | 8 | HG00735.hp2 HG01255.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.5-338A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 1/9 | chrX | 107840332 | ||||||
| chrX:107841402
|
G | A | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02622.hp2 HG02976.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+17G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107841402 | ||||||
| chrX:107841423
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.720+38C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107841423 | ||||||
| chrX:107842630
|
G | A | 2 | a0001c0001t0003g0177a0001c0001t0009g0026 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.720+1245G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107842630 | ||||||
| chrX:107842656
|
G | T | 10 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(7): Show | 10 | HG01109.hp1 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+1271G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107842656 | ||||||
| chrX:107842911
|
G | C | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.720+1526G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107842911 | ||||||
| chrX:107843333
|
A | G | 7 | a0001c0001t0001g0165a0001c0001t0007g0139a0001c0001t0007g0166others(4): Show | 7 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.720+1948A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843333 | ||||||
| chrX:107843338
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.720+1953C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843338 | ||||||
| chrX:107843474
|
G | A | 2 | a0001c0002t0006g0179a0001c0002t0006g0180 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.720+2089G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843474 | ||||||
| chrX:107843491
|
T | A | 12 | a0001c0001t0002g0021a0001c0001t0005g0016a0001c0001t0005g0017others(9): Show | 12 | HG01243.hp1 HG02886.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.720+2106T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843491 | ||||||
| chrX:107843612
|
T | C | 3 | a0001c0001t0002g0132a0001c0001t0008g0134a0001c0001t0010g0133 | 3 | HG01891.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.720+2227T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843612 | ||||||
| chrX:107843673
|
C | T | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.720+2288C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843673 | ||||||
| chrX:107843799
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.720+2414G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843799 | ||||||
| chrX:107843813
|
G | A | 12 | a0001c0001t0002g0021a0001c0001t0005g0016a0001c0001t0005g0017others(9): Show | 12 | HG01243.hp1 HG02886.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.720+2428G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843813 | ||||||
| chrX:107843866
|
G | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+2481G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843866 | ||||||
| chrX:107843873
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0113a0001c0001t0001g0181others(1): Show | 4 | HG02055.hp1 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2488G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843873 | ||||||
| chrX:107843950
|
A | G | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.720+2565A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107843950 | ||||||
| chrX:107844230
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.720+2845G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107844230 | ||||||
| chrX:107844468
|
T | G | 10 | a0001c0001t0002g0178a0001c0001t0012g0173a0002c0003t0002g0138others(7): Show | 10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+3083T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107844468 | ||||||
| chrX:107844548
|
A | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+3163A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107844548 | ||||||
| chrX:107844737
|
C | CCTAA | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 90 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.720+3354_720+3355i others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107844737 | |||||
| chrX:107844905
|
G | T | 1 | a0001c0001t0008g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.720+3520G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107844905 | ||||||
| chrX:107845024
|
G | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0105others(1): Show | 4 | NA18747.hp1 NA18975.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+3639G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845024 | ||||||
| chrX:107845039
|
T | A | 2 | a0001c0002t0006g0179a0001c0002t0006g0180 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.720+3654T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845039 | ||||||
| chrX:107845039
|
T | G | 49 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0038others(46): Show | 49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.720+3654T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845039 | ||||||
| chrX:107845451
|
T | C | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.720+4066T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845451 | ||||||
| chrX:107845492
|
A | AAC | 5 | a0001c0001t0001g0002a0001c0001t0001g0064a0001c0001t0004g0032others(2): Show | 5 | HG00280.hp1 HG03540.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+4140_720+4141d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845492 | |||||
| chrX:107845492
|
A | AACAC | 3 | a0001c0001t0001g0034a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | HG01069.hp1 HG01071.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.720+4138_720+4141d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845492 | |||||
| chrX:107845492
|
A | AC | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.720+4107_720+4108i others(3): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845492 | ||||||
| chrX:107845492
|
AAC | A | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.720+4140_720+4141d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845492 | |||||
| chrX:107845492
|
AACACACA others(5): Show |
A | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.720+4130_720+4141d others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845492 | |||||
| chrX:107845517
|
A | ACTCT | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.720+4133_720+4134i others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845517 | |||||
| chrX:107845517
|
A | ACTCTCTC others(1): Show |
1 | a0001c0002t0002g0140 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.720+4133_720+4134i others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845517 | |||||
| chrX:107845519
|
A | ACT | 4 | a0001c0001t0002g0178a0001c0001t0012g0173a0002c0003t0002g0163others(1): Show | 4 | HG00741.hp2 HG01071.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4135_720+4136i others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845519 | |||||
| chrX:107845519
|
A | ACTCT | 1 | a0002c0003t0002g0170 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.720+4135_720+4136i others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845519 | |||||
| chrX:107845519
|
A | T | 2 | a0001c0002t0002g0140a0003c0007t0002g0131 | 2 | HG01168.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.720+4134A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845519 | ||||||
| chrX:107845521
|
A | ACT | 1 | a0002c0003t0002g0138 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.720+4137_720+4138i others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | |||||
| chrX:107845521
|
A | ACTCT | 2 | a0001c0002t0002g0141a0002c0003t0002g0159 | 2 | HG03704.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.720+4137_720+4138i others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | |||||
| chrX:107845521
|
A | ACTCTCT | 3 | a0001c0001t0006g0023a0001c0001t0006g0024a0001c0006t0002g0128 | 3 | HG02738.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.720+4137_720+4138i others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | |||||
| chrX:107845521
|
A | ACTCTCTC others(1): Show |
6 | a0001c0001t0002g0132a0001c0001t0003g0007a0001c0001t0014g0171others(3): Show | 6 | HG01168.hp1 HG01891.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4137_720+4138i others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | |||||
| chrX:107845521
|
A | ACTCTCTC others(3): Show |
15 | a0001c0001t0002g0006a0001c0001t0002g0046a0001c0001t0002g0050others(12): Show | 15 | HG00558.hp1 HG00609.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+4137_720+4138i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | |||||
| chrX:107845521
|
A | ACTCTCTC others(5): Show |
3 | a0001c0001t0002g0112a0001c0002t0002g0137a0001c0002t0002g0148 | 3 | HG02165.hp1 HG03471.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.720+4137_720+4138i others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | |||||
| chrX:107845521
|
A | ACTCTCTC others(7): Show |
2 | a0001c0002t0002g0149a0001c0002t0002g0150 | 2 | NA18973.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.720+4137_720+4138i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845521 | |||||
| chrX:107845521
|
A | T | 10 | a0001c0001t0002g0178a0001c0001t0012g0173a0001c0002t0002g0140others(7): Show | 10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.720+4136A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845521 | ||||||
| chrX:107845523
|
A | ACTCTCT | 3 | a0001c0001t0001g0120a0001c0001t0010g0123a0001c0001t0010g0133 | 3 | HG02486.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.720+4139_720+4140i others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845523 | |||||
| chrX:107845523
|
A | ACTCTCTC others(1): Show |
1 | a0001c0001t0006g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.720+4139_720+4140i others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845523 | |||||
| chrX:107845523
|
A | ACTCTCTC others(3): Show |
1 | a0001c0001t0002g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.720+4139_720+4140i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845523 | |||||
| chrX:107845523
|
A | ACTCTCTC others(7): Show |
1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.720+4139_720+4140i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845523 | |||||
| chrX:107845523
|
A | T | 47 | a0001c0001t0002g0006a0001c0001t0002g0038a0001c0001t0002g0046others(44): Show | 47 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.720+4138A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845523 | ||||||
| chrX:107845525
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0005g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0003g0008 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(20): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0003g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(22): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACAC others(25): Show |
1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(34): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACTC others(5): Show |
4 | a0001c0001t0005g0017a0001c0001t0005g0018a0001c0001t0005g0027others(1): Show | 4 | HG02922.hp1 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+4141_720+4142i others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACTC others(7): Show |
1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACTC others(9): Show |
2 | a0001c0001t0005g0020a0001c0002t0009g0176 | 2 | HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.720+4141_720+4142i others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACTC others(11): Show |
2 | a0001c0001t0003g0010a0001c0001t0003g0015 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.720+4141_720+4142i others(20): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACACTC others(23): Show |
1 | a0001c0001t0003g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(32): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACTCT | 1 | a0001c0001t0001g0041 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACTCTC others(7): Show |
1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACTCTC others(9): Show |
1 | a0001c0002t0001g0154 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACTCTC others(11): Show |
1 | a0001c0001t0003g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(20): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACTCTC others(21): Show |
1 | a0001c0001t0001g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.720+4141_720+4142i others(30): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACTCTC others(23): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0175a0001c0001t0003g0012 | 3 | HG02970.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.720+4141_720+4142i others(32): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACTCTC others(25): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.720+4141_720+4142i others(34): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACACTCTC others(27): Show |
1 | a0001c0002t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.720+4141_720+4142i others(36): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACT | 2 | a0001c0001t0001g0043a0001c0001t0004g0098 | 2 | HG03041.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.720+4172_720+4173d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACTCT | 2 | a0001c0001t0001g0042a0001c0001t0007g0169 | 2 | HG02258.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.720+4170_720+4173d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACTCTCTC others(1): Show |
6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+4166_720+4173d others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACTCTCTC others(5): Show |
1 | a0001c0002t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.720+4162_720+4173d others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACTCTCTC others(7): Show |
1 | a0001c0002t0001g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.720+4160_720+4173d others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | ACTCTCTC others(9): Show |
2 | a0001c0002t0001g0156a0001c0002t0001g0157 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.720+4158_720+4173d others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845525
|
A | T | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0040others(59): Show | 62 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.720+4140A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845525 | ||||||
| chrX:107845525
|
ACTCT | A | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.720+4170_720+4173d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845525 | |||||
| chrX:107845527
|
T | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(3): Show | 6 | HG00738.hp1 HG00741.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+4142T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845527 | ||||||
| chrX:107845540
|
C | CTCTCTCT others(3): Show |
2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.720+4164_720+4165i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107845540 | |||||
| chrX:107845876
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0043 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.720+4491G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845876 | ||||||
| chrX:107845980
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.720+4595C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107845980 | ||||||
| chrX:107846003
|
T | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.720+4618T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846003 | ||||||
| chrX:107846071
|
G | C | 1 | a0001c0001t0001g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.720+4686G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846071 | ||||||
| chrX:107846381
|
A | G | 6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+4996A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846381 | ||||||
| chrX:107846515
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.720+5130C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846515 | ||||||
| chrX:107846700
|
G | A | 3 | a0001c0001t0002g0132a0001c0001t0003g0012a0001c0001t0003g0126 | 3 | HG01109.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.720+5315G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846700 | ||||||
| chrX:107846709
|
T | C | 1 | a0001c0002t0009g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.720+5324T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846709 | ||||||
| chrX:107846835
|
A | G | 1 | a0001c0001t0005g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.720+5450A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846835 | ||||||
| chrX:107846965
|
A | G | 3 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053 | 3 | HG00609.hp1 NA18948.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.720+5580A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107846965 | ||||||
| chrX:107847004
|
A | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 94 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.720+5619A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107847004 | ||||||
| chrX:107847113
|
G | A | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.720+5728G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107847113 | ||||||
| chrX:107848771
|
A | G | 1 | a0001c0001t0004g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.721-5838A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107848771 | ||||||
| chrX:107849033
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 179 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.721-5576A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849033 | ||||||
| chrX:107849341
|
G | C | 1 | a0001c0001t0002g0046 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.721-5268G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849341 | ||||||
| chrX:107849348
|
T | C | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.721-5261T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849348 | ||||||
| chrX:107849429
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.721-5180A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849429 | ||||||
| chrX:107849488
|
A | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0096others(1): Show | 4 | HG00280.hp1 HG01516.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-5121A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107849488 | ||||||
| chrX:107850189
|
G | GAC | 1 | a0001c0001t0013g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.721-4393_721-4392d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107850189 | |||||
| chrX:107850189
|
GACAC | G | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.721-4395_721-4392d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107850189 | |||||
| chrX:107850189
|
GACACAC | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 92 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.721-4397_721-4392d others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107850189 | |||||
| chrX:107850217
|
C | CA | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.721-4392_721-4391i others(3): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107850217 | ||||||
| chrX:107850426
|
A | G | 8 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(5): Show | 8 | HG01109.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.721-4183A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107850426 | ||||||
| chrX:107850590
|
T | C | 1 | a0002c0003t0002g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.721-4019T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107850590 | ||||||
| chrX:107851476
|
A | G | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-3133A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851476 | ||||||
| chrX:107851552
|
A | G | 1 | a0001c0001t0006g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.721-3057A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851552 | ||||||
| chrX:107851652
|
A | AAAC | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.721-2930_721-2928d others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851652 | |||||
| chrX:107851707
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0112a0001c0002t0002g0143 | 3 | HG02976.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.721-2902A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851707 | ||||||
| chrX:107851767
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 94 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.721-2842G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851767 | ||||||
| chrX:107851780
|
C | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(76): Show | 79 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.721-2829C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107851780 | ||||||
| chrX:107851853
|
CTTTTTAT others(5): Show |
C | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.721-2754_721-2743d others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851853 | |||||
| chrX:107851855
|
T | TTTTA | 2 | a0001c0002t0002g0137a0001c0002t0002g0143 | 2 | HG02165.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.721-2711_721-2708d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | |||||
| chrX:107851855
|
TTTTA | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0030others(111): Show | 114 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.721-2711_721-2708d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | |||||
| chrX:107851855
|
TTTTATTT others(1): Show |
T | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(10): Show | 13 | HG01243.hp1 HG01516.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.721-2715_721-2708d others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | |||||
| chrX:107851855
|
TTTTATTT others(5): Show |
T | 9 | a0001c0001t0002g0132a0001c0001t0003g0007a0001c0001t0003g0008others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.721-2719_721-2708d others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | |||||
| chrX:107851855
|
TTTTATTT others(9): Show |
T | 9 | a0001c0001t0001g0135a0001c0001t0005g0016a0001c0001t0005g0017others(6): Show | 9 | HG02922.hp1 HG02965.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.721-2723_721-2708d others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | |||||
| chrX:107851855
|
TTTTATTT others(13): Show |
T | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-2727_721-2708d others(22): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | |||||
| chrX:107851855
|
TTTTATTT others(17): Show |
T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.721-2731_721-2708d others(26): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 107851855 | |||||
| chrX:107852143
|
C | T | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.721-2466C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107852143 | ||||||
| chrX:107852866
|
G | A | 1 | a0002c0003t0002g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.721-1743G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107852866 | ||||||
| chrX:107852924
|
C | T | 1 | a0001c0002t0009g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.721-1685C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107852924 | ||||||
| chrX:107853108
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.721-1501A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853108 | ||||||
| chrX:107853112
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.721-1497A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853112 | ||||||
| chrX:107853141
|
C | G | 18 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-1468C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853141 | ||||||
| chrX:107853188
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0126 | 2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.721-1421G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853188 | ||||||
| chrX:107853424
|
T | G | 1 | a0001c0002t0009g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.721-1185T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853424 | ||||||
| chrX:107853538
|
G | A | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.721-1071G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853538 | ||||||
| chrX:107853590
|
G | A | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.721-1019G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853590 | ||||||
| chrX:107853931
|
C | G | 4 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 4 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-678C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853931 | ||||||
| chrX:107853951
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.721-658A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107853951 | ||||||
| chrX:107854026
|
T | C | 18 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-583T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854026 | ||||||
| chrX:107854138
|
T | G | 5 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.721-471T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854138 | ||||||
| chrX:107854206
|
A | G | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.721-403A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854206 | ||||||
| chrX:107854308
|
T | C | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-301T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854308 | ||||||
| chrX:107854452
|
G | C | 18 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-157G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854452 | ||||||
| chrX:107854541
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.721-68T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 2/9 | chrX | 107854541 | ||||||
| chrX:107854897
|
C | T | 11 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 11 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+193C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107854897 | ||||||
| chrX:107854911
|
A | G | 18 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+207A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107854911 | ||||||
| chrX:107854966
|
A | G | 18 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+262A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107854966 | ||||||
| chrX:107854999
|
A | G | 1 | a0001c0002t0002g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.816+295A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107854999 | ||||||
| chrX:107855176
|
A | G | 32 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0046others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.816+472A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107855176 | ||||||
| chrX:107855696
|
A | G | 11 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 11 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+992A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107855696 | ||||||
| chrX:107855882
|
C | T | 18 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+1178C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107855882 | ||||||
| chrX:107856091
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.816+1387G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107856091 | ||||||
| chrX:107857183
|
T | C | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.816+2479T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107857183 | ||||||
| chrX:107857207
|
G | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+2503G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107857207 | ||||||
| chrX:107857281
|
C | CT | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+2594dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107857281 | |||||
| chrX:107857281
|
CT | C | 3 | a0001c0001t0001g0070a0001c0001t0003g0177a0001c0002t0002g0151 | 3 | HG02451.hp1 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.816+2594delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107857281 | |||||
| chrX:107857593
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.816+2889A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107857593 | ||||||
| chrX:107857784
|
A | G | 16 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 16 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.816+3080A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107857784 | ||||||
| chrX:107858104
|
C | A | 2 | a0001c0001t0005g0017a0001c0001t0005g0019 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.816+3400C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858104 | ||||||
| chrX:107858123
|
A | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+3419A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858123 | ||||||
| chrX:107858527
|
T | C | 1 | a0001c0001t0004g0115 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.816+3823T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858527 | ||||||
| chrX:107858553
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.816+3849C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858553 | ||||||
| chrX:107858733
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.816+4029T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107858733 | ||||||
| chrX:107859068
|
A | G | 18 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(15): Show | 18 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.816+4364A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859068 | ||||||
| chrX:107859184
|
C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 59 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.816+4480C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859184 | ||||||
| chrX:107859473
|
G | A | 2 | a0001c0002t0006g0179a0001c0002t0006g0180 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.816+4769G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859473 | ||||||
| chrX:107859677
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+4973C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859677 | ||||||
| chrX:107859700
|
G | C | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.816+4996G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859700 | ||||||
| chrX:107859919
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+5215A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107859919 | ||||||
| chrX:107860126
|
G | A | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816+5422G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107860126 | ||||||
| chrX:107861045
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(13): Show | 16 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.816+6341T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861045 | ||||||
| chrX:107861468
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+6764A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861468 | ||||||
| chrX:107861472
|
T | C | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+6768T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861472 | ||||||
| chrX:107861743
|
A | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0134 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.816+7039A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861743 | ||||||
| chrX:107861889
|
T | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(2): Show | 5 | HG00280.hp1 HG01516.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+7185T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861889 | ||||||
| chrX:107861987
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+7283A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107861987 | ||||||
| chrX:107862235
|
A | G | 1 | a0001c0006t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.816+7531A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107862235 | ||||||
| chrX:107862784
|
T | C | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+8080T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107862784 | ||||||
| chrX:107863141
|
T | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+8437T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107863141 | ||||||
| chrX:107863325
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+8621C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107863325 | ||||||
| chrX:107863560
|
C | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.816+8856C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107863560 | ||||||
| chrX:107863978
|
C | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0102 | 2 | HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.816+9274C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107863978 | ||||||
| chrX:107864086
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+9382T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864086 | ||||||
| chrX:107864136
|
C | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0134 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.816+9432C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864136 | ||||||
| chrX:107864301
|
A | G | 2 | a0001c0002t0002g0137a0001c0002t0002g0147 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.816+9597A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864301 | ||||||
| chrX:107864302
|
C | A | 2 | a0001c0002t0002g0137a0001c0002t0002g0147 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.816+9598C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864302 | ||||||
| chrX:107864714
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0113 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.816+10010A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864714 | ||||||
| chrX:107864726
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.816+10022A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107864726 | ||||||
| chrX:107865131
|
C | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+10427C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865131 | ||||||
| chrX:107865131
|
C | T | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+10427C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865131 | ||||||
| chrX:107865161
|
T | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+10457T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865161 | ||||||
| chrX:107865545
|
C | CCT | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+10842_816+1084 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107865545 | |||||
| chrX:107865573
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+10869G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865573 | ||||||
| chrX:107865573
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.816+10869G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865573 | ||||||
| chrX:107865605
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.816+10901A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865605 | ||||||
| chrX:107865655
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+10951T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865655 | ||||||
| chrX:107865758
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.816+11054C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865758 | ||||||
| chrX:107865764
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+11060C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865764 | ||||||
| chrX:107865839
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+11135A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865839 | ||||||
| chrX:107865993
|
G | C | 1 | a0001c0002t0009g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.816+11289G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865993 | ||||||
| chrX:107865995
|
G | T | 5 | a0002c0003t0002g0138a0002c0003t0002g0159a0002c0003t0002g0160others(2): Show | 5 | HG01515.hp1 HG01516.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+11291G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107865995 | ||||||
| chrX:107866070
|
C | T | 4 | a0001c0001t0002g0056a0001c0002t0002g0136a0001c0002t0002g0141others(1): Show | 4 | NA18944.hp1 NA18945.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+11366C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107866070 | ||||||
| chrX:107866225
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.816+11521A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107866225 | ||||||
| chrX:107866419
|
GA | G | 1 | a0001c0001t0003g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.816+11719delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866419 | |||||
| chrX:107866421
|
AAACAC | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0008g0014 | 3 | HG02630.hp1 HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.816+11719_816+1172 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866421 | |||||
| chrX:107866422
|
A | AAC | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0003g0010others(1): Show | 4 | HG02572.hp1 HG02723.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+11772_816+1177 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
A | AACAC | 2 | a0001c0001t0001g0089a0001c0001t0013g0114 | 2 | HG04199.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.816+11770_816+1177 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AAC | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0102a0001c0001t0001g0175 | 3 | HG01433.hp1 HG03704.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.816+11772_816+1177 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACAC | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0066others(13): Show | 16 | HG00642.hp1 HG01099.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.816+11770_816+1177 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACACAC | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(55): Show | 58 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.816+11768_816+1177 others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACACACA others(1): Show |
A | 20 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 20 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.816+11766_816+1177 others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACACACA others(3): Show |
A | 20 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0072others(17): Show | 20 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.816+11764_816+1177 others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACACACA others(5): Show |
A | 29 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0046others(26): Show | 29 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.816+11762_816+1177 others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACACACA others(7): Show |
A | 2 | a0001c0001t0003g0177a0001c0001t0014g0171 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.816+11760_816+1177 others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACACACA others(9): Show |
A | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.816+11758_816+1177 others(20): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACACACA others(13): Show |
A | 4 | a0001c0001t0006g0022a0001c0001t0006g0024a0001c0002t0006g0179others(1): Show | 4 | HG01243.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+11754_816+1177 others(24): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866422
|
AACACACA others(15): Show |
A | 12 | a0001c0001t0002g0038a0001c0001t0002g0178a0001c0001t0006g0023others(9): Show | 12 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.816+11752_816+1177 others(26): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866422 | |||||
| chrX:107866464
|
CACACACA others(6): Show |
C | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.816+11765_816+1177 others(17): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107866464 | |||||
| chrX:107866817
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+12113A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107866817 | ||||||
| chrX:107867317
|
A | AT | 1 | a0001c0001t0013g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.816+12630dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107867317 | |||||
| chrX:107867317
|
AT | A | 36 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0121others(33): Show | 36 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.816+12630delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107867317 | |||||
| chrX:107867317
|
ATT | A | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+12629_816+1263 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107867317 | |||||
| chrX:107867335
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+12631G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867335 | ||||||
| chrX:107867493
|
C | A | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816+12789C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867493 | ||||||
| chrX:107867514
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.816+12810A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867514 | ||||||
| chrX:107867764
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+13060A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867764 | ||||||
| chrX:107867978
|
A | T | 49 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0038others(46): Show | 49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.816+13274A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107867978 | ||||||
| chrX:107868003
|
A | G | 35 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(32): Show | 35 | HG01106.hp1 HG01109.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.816+13299A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107868003 | ||||||
| chrX:107868178
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+13474T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107868178 | ||||||
| chrX:107868219
|
T | C | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+13515T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107868219 | ||||||
| chrX:107868389
|
A | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124 | 3 | HG02622.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.816+13685A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107868389 | ||||||
| chrX:107869091
|
G | A | 2 | a0001c0001t0007g0139a0001c0001t0007g0166 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.816+14387G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869091 | ||||||
| chrX:107869485
|
T | G | 1 | a0001c0001t0008g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.816+14781T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869485 | ||||||
| chrX:107869590
|
G | T | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+14886G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869590 | ||||||
| chrX:107869712
|
T | C | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+15008T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869712 | ||||||
| chrX:107869833
|
TA | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+15139delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107869833 | |||||
| chrX:107869838
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+15134A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869838 | ||||||
| chrX:107869882
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.816+15178T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107869882 | ||||||
| chrX:107870060
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+15356T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107870060 | ||||||
| chrX:107870222
|
T | G | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+15518T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107870222 | ||||||
| chrX:107870519
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+15815G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107870519 | ||||||
| chrX:107870621
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0062 | 2 | HG02698.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.816+15917G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107870621 | ||||||
| chrX:107870753
|
C | CT | 51 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0049others(48): Show | 51 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.816+16067dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | |||||
| chrX:107870753
|
C | CTT | 8 | a0001c0001t0001g0124a0001c0001t0002g0091a0001c0002t0001g0154others(5): Show | 8 | HG02572.hp1 HG02738.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+16066_816+1606 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | |||||
| chrX:107870753
|
C | CTTT | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0174others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+16065_816+1606 others(7): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | |||||
| chrX:107870753
|
C | CTTTT | 8 | a0001c0001t0001g0005a0001c0001t0005g0016a0001c0001t0005g0017others(5): Show | 8 | HG02145.hp1 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+16064_816+1606 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | |||||
| chrX:107870753
|
C | CTTTTT | 1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.816+16063_816+1606 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | |||||
| chrX:107870753
|
CT | C | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.816+16067delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107870753 | |||||
| chrX:107871023
|
T | C | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+16319T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871023 | ||||||
| chrX:107871258
|
C | T | 1 | a0001c0006t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.816+16554C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871258 | ||||||
| chrX:107871282
|
G | A | 2 | a0001c0001t0010g0123a0001c0001t0010g0133 | 2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.816+16578G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871282 | ||||||
| chrX:107871317
|
C | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.816+16613C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871317 | ||||||
| chrX:107871386
|
G | A | 32 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0046others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.816+16682G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871386 | ||||||
| chrX:107871400
|
G | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+16696G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871400 | ||||||
| chrX:107871499
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.816+16795A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871499 | ||||||
| chrX:107871527
|
T | C | 10 | a0001c0001t0001g0165a0001c0001t0003g0007a0001c0001t0003g0008others(7): Show | 10 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+16823T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871527 | ||||||
| chrX:107871726
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.816+17022A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871726 | ||||||
| chrX:107871760
|
C | T | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.816+17056C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871760 | ||||||
| chrX:107871783
|
T | G | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816+17079T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871783 | ||||||
| chrX:107871786
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+17082T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871786 | ||||||
| chrX:107871811
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+17107A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871811 | ||||||
| chrX:107871868
|
C | A | 1 | a0001c0002t0002g0152 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.816+17164C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107871868 | ||||||
| chrX:107872020
|
C | T | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+17316C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107872020 | ||||||
| chrX:107872214
|
CCTGA | C | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+17514_816+1751 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107872214 | |||||
| chrX:107872254
|
A | G | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+17550A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107872254 | ||||||
| chrX:107872320
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+17616A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107872320 | ||||||
| chrX:107872801
|
A | G | 1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.816+18097A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107872801 | ||||||
| chrX:107873505
|
T | C | 1 | a0001c0001t0007g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.816+18801T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107873505 | ||||||
| chrX:107874245
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.816+19541A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107874245 | ||||||
| chrX:107874388
|
G | GT | 1 | a0001c0002t0001g0146 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.816+19686dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107874388 | |||||
| chrX:107874492
|
T | A | 11 | a0001c0001t0002g0178a0001c0001t0012g0173a0002c0003t0002g0138others(8): Show | 11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+19788T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107874492 | ||||||
| chrX:107875258
|
C | G | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+20554C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875258 | ||||||
| chrX:107875391
|
C | G | 32 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0046others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.816+20687C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875391 | ||||||
| chrX:107875657
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124 | 3 | HG02622.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.816+20953G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875657 | ||||||
| chrX:107875829
|
T | C | 15 | a0001c0001t0001g0165a0001c0001t0005g0016a0001c0001t0005g0017others(12): Show | 15 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.816+21125T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875829 | ||||||
| chrX:107875864
|
C | T | 1 | a0001c0001t0010g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.816+21160C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875864 | ||||||
| chrX:107875893
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+21189T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107875893 | ||||||
| chrX:107876142
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.816+21438C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876142 | ||||||
| chrX:107876277
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.816+21573A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876277 | ||||||
| chrX:107876409
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.816+21705A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876409 | ||||||
| chrX:107876685
|
TCAGCTG | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0102 | 2 | HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.816+21985_816+2199 others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107876685 | |||||
| chrX:107876719
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.816+22015G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876719 | ||||||
| chrX:107876888
|
A | G | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+22184A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107876888 | ||||||
| chrX:107877178
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+22474G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107877178 | ||||||
| chrX:107877694
|
T | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+22990T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107877694 | ||||||
| chrX:107878012
|
GA | G | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+23320delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107878012 | |||||
| chrX:107878062
|
A | T | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+23358A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107878062 | ||||||
| chrX:107878358
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+23654A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107878358 | ||||||
| chrX:107878640
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.816+23936C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107878640 | ||||||
| chrX:107878939
|
T | C | 1 | a0001c0001t0008g0014 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.816+24235T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107878939 | ||||||
| chrX:107879107
|
G | A | 1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.816+24403G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107879107 | ||||||
| chrX:107879187
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.816+24483T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107879187 | ||||||
| chrX:107879243
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.816+24539G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107879243 | ||||||
| chrX:107879528
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-24430C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107879528 | ||||||
| chrX:107879931
|
GT | G | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.817-24020delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107879931 | |||||
| chrX:107880246
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-23712C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880246 | ||||||
| chrX:107880329
|
CA | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA18986.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.817-23627delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107880329 | |||||
| chrX:107880360
|
G | A | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-23598G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880360 | ||||||
| chrX:107880558
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.817-23400A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880558 | ||||||
| chrX:107880571
|
C | CA | 1 | a0001c0002t0002g0151 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.817-23380dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107880571 | |||||
| chrX:107880682
|
G | A | 7 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-23276G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880682 | ||||||
| chrX:107880921
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-23037A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107880921 | ||||||
| chrX:107881146
|
T | C | 9 | a0002c0003t0002g0138a0002c0003t0002g0159a0002c0003t0002g0160others(6): Show | 9 | HG00735.hp2 HG01168.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-22812T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881146 | ||||||
| chrX:107881468
|
T | C | 1 | a0001c0002t0002g0152 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.817-22490T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881468 | ||||||
| chrX:107881477
|
C | T | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0134 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.817-22481C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881477 | ||||||
| chrX:107881480
|
A | G | 1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.817-22478A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881480 | ||||||
| chrX:107881506
|
G | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-22452G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881506 | ||||||
| chrX:107881684
|
G | A | 2 | a0001c0001t0008g0013a0001c0001t0008g0014 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.817-22274G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881684 | ||||||
| chrX:107881701
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.817-22257A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881701 | ||||||
| chrX:107881739
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-22219A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881739 | ||||||
| chrX:107881757
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.817-22201C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881757 | ||||||
| chrX:107881831
|
T | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-22127T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881831 | ||||||
| chrX:107881863
|
A | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.817-22095A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107881863 | ||||||
| chrX:107882047
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0043 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.817-21911C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882047 | ||||||
| chrX:107882372
|
A | G | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-21586A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882372 | ||||||
| chrX:107882456
|
T | C | 2 | a0001c0001t0002g0132a0001c0001t0014g0171 | 2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.817-21502T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882456 | ||||||
| chrX:107882505
|
G | GA | 15 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(12): Show | 15 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.817-21445dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107882505 | |||||
| chrX:107882555
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-21403C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882555 | ||||||
| chrX:107882774
|
C | G | 49 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0038others(46): Show | 49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.817-21184C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882774 | ||||||
| chrX:107882892
|
G | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-21066G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882892 | ||||||
| chrX:107882958
|
C | G | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.817-21000C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107882958 | ||||||
| chrX:107883013
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-20945A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883013 | ||||||
| chrX:107883075
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-20883A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883075 | ||||||
| chrX:107883088
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-20870A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883088 | ||||||
| chrX:107883233
|
G | A | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-20725G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883233 | ||||||
| chrX:107883385
|
A | C | 6 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(3): Show | 6 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-20573A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883385 | ||||||
| chrX:107883397
|
T | A | 1 | a0001c0001t0014g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.817-20561T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107883397 | ||||||
| chrX:107884115
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.817-19843T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884115 | ||||||
| chrX:107884398
|
T | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-19560T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884398 | ||||||
| chrX:107884614
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-19344C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884614 | ||||||
| chrX:107884683
|
C | CA | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-19270dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107884683 | |||||
| chrX:107884684
|
A | AAAAAC | 2 | a0001c0001t0001g0047a0001c0001t0001g0102 | 2 | HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.817-19254_817-1925 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107884684 | |||||
| chrX:107884728
|
A | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.817-19230A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884728 | ||||||
| chrX:107884747
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.817-19211C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884747 | ||||||
| chrX:107884878
|
T | C | 1 | a0001c0001t0004g0032 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.817-19080T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107884878 | ||||||
| chrX:107885093
|
G | GGAGA | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.817-18864_817-1886 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107885093 | |||||
| chrX:107885102
|
C | CTTAT | 3 | a0001c0002t0002g0149a0001c0002t0006g0179a0001c0002t0006g0180 | 3 | HG02647.hp1 HG03225.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.817-18829_817-1882 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107885102 | |||||
| chrX:107885102
|
C | CTTATTTA others(1): Show |
4 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 4 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-18833_817-1882 others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107885102 | |||||
| chrX:107885102
|
C | CTTATTTA others(5): Show |
2 | a0001c0001t0001g0113a0001c0001t0007g0169 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.817-18837_817-1882 others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107885102 | |||||
| chrX:107885386
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18572T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885386 | ||||||
| chrX:107885391
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-18567G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885391 | ||||||
| chrX:107885402
|
G | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18556G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885402 | ||||||
| chrX:107885518
|
T | A | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.817-18440T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885518 | ||||||
| chrX:107885645
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.817-18313G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885645 | ||||||
| chrX:107885655
|
A | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18303A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885655 | ||||||
| chrX:107885719
|
A | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18239A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885719 | ||||||
| chrX:107885720
|
G | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-18238G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885720 | ||||||
| chrX:107885776
|
G | A | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-18182G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885776 | ||||||
| chrX:107885893
|
T | C | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-18065T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885893 | ||||||
| chrX:107885969
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-17989A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107885969 | ||||||
| chrX:107886025
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-17933C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886025 | ||||||
| chrX:107886119
|
T | G | 33 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0038others(30): Show | 33 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.817-17839T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886119 | ||||||
| chrX:107886337
|
C | A | 1 | a0001c0002t0002g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.817-17621C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886337 | ||||||
| chrX:107886394
|
G | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-17564G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886394 | ||||||
| chrX:107886559
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.817-17399T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886559 | ||||||
| chrX:107886790
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.817-17168T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886790 | ||||||
| chrX:107886808
|
T | G | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.817-17150T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886808 | ||||||
| chrX:107886945
|
A | G | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(2): Show | 5 | HG00280.hp1 HG01516.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-17013A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886945 | ||||||
| chrX:107886955
|
A | T | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-17003A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107886955 | ||||||
| chrX:107887177
|
A | C | 10 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(7): Show | 10 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-16781A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887177 | ||||||
| chrX:107887202
|
A | C | 1 | a0001c0001t0003g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.817-16756A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887202 | ||||||
| chrX:107887254
|
G | A | 1 | a0001c0001t0003g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-16704G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887254 | ||||||
| chrX:107887300
|
C | G | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-16658C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887300 | ||||||
| chrX:107887306
|
C | A | 1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.817-16652C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887306 | ||||||
| chrX:107887335
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0126 | 2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.817-16623G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887335 | ||||||
| chrX:107887385
|
C | G | 10 | a0001c0001t0001g0165a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-16573C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887385 | ||||||
| chrX:107887496
|
G | C | 9 | a0002c0003t0002g0138a0002c0003t0002g0159a0002c0003t0002g0160others(6): Show | 9 | HG00735.hp2 HG01168.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-16462G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887496 | ||||||
| chrX:107887671
|
A | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0102 | 2 | HG01433.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.817-16287A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887671 | ||||||
| chrX:107887856
|
A | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 59 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.817-16102A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107887856 | ||||||
| chrX:107888528
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-15430A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107888528 | ||||||
| chrX:107888686
|
C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 59 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.817-15272C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107888686 | ||||||
| chrX:107888942
|
A | C | 34 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(31): Show | 34 | HG01106.hp1 HG01109.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.817-15016A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107888942 | ||||||
| chrX:107889044
|
A | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-14914A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889044 | ||||||
| chrX:107889075
|
A | G | 5 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-14883A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889075 | ||||||
| chrX:107889221
|
G | T | 3 | a0001c0001t0002g0091a0001c0002t0002g0137a0001c0002t0002g0147 | 3 | HG02056.hp1 HG02165.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.817-14737G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889221 | ||||||
| chrX:107889409
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0014g0171 | 2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.817-14549G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889409 | ||||||
| chrX:107889410
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.817-14548G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889410 | ||||||
| chrX:107889481
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.817-14477G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889481 | ||||||
| chrX:107889489
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-14469C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889489 | ||||||
| chrX:107889606
|
C | A | 11 | a0001c0001t0002g0178a0001c0001t0012g0173a0002c0003t0002g0138others(8): Show | 11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.817-14352C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889606 | ||||||
| chrX:107889738
|
G | A | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-14220G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889738 | ||||||
| chrX:107889748
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-14210G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889748 | ||||||
| chrX:107889809
|
G | A | 1 | a0001c0001t0003g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.817-14149G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889809 | ||||||
| chrX:107889948
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.817-14010T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107889948 | ||||||
| chrX:107890022
|
AT | A | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.817-13928delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107890022 | |||||
| chrX:107890873
|
T | C | 1 | a0001c0001t0008g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.817-13085T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107890873 | ||||||
| chrX:107891072
|
C | T | 2 | a0001c0002t0002g0137a0001c0002t0002g0147 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.817-12886C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891072 | ||||||
| chrX:107891081
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-12877A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891081 | ||||||
| chrX:107891121
|
C | T | 6 | a0001c0001t0002g0006a0001c0001t0002g0046a0001c0001t0002g0050others(3): Show | 6 | HG00558.hp1 HG00609.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-12837C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891121 | ||||||
| chrX:107891201
|
G | A | 1 | a0001c0001t0004g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.817-12757G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891201 | ||||||
| chrX:107891279
|
C | CT | 6 | a0001c0001t0001g0086a0001c0001t0002g0091a0001c0002t0001g0154others(3): Show | 6 | HG02572.hp1 HG02886.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-12660dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107891279 | |||||
| chrX:107891279
|
C | CTT | 1 | a0001c0002t0001g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.817-12661_817-1266 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107891279 | |||||
| chrX:107891279
|
CT | C | 16 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0057others(13): Show | 16 | HG01069.hp1 HG01891.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.817-12660delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107891279 | |||||
| chrX:107891342
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0134 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.817-12616G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891342 | ||||||
| chrX:107891405
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-12553C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891405 | ||||||
| chrX:107891429
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-12529C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891429 | ||||||
| chrX:107891505
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-12453C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891505 | ||||||
| chrX:107891525
|
C | T | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-12433C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891525 | ||||||
| chrX:107891722
|
T | C | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.817-12236T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891722 | ||||||
| chrX:107891823
|
C | G | 1 | a0001c0002t0009g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.817-12135C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107891823 | ||||||
| chrX:107892201
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.817-11757C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892201 | ||||||
| chrX:107892349
|
A | G | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-11609A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892349 | ||||||
| chrX:107892382
|
T | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-11576T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892382 | ||||||
| chrX:107892534
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.817-11424C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892534 | ||||||
| chrX:107892762
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-11196A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892762 | ||||||
| chrX:107892785
|
C | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-11173C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107892785 | ||||||
| chrX:107893049
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-10909A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893049 | ||||||
| chrX:107893163
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 94 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.817-10795A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893163 | ||||||
| chrX:107893275
|
A | G | 1 | a0001c0002t0002g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.817-10683A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893275 | ||||||
| chrX:107893659
|
A | G | 1 | a0001c0001t0003g0010 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.817-10299A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893659 | ||||||
| chrX:107893858
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.817-10100T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107893858 | ||||||
| chrX:107894012
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.817-9946C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894012 | ||||||
| chrX:107894016
|
ACCT | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-9938_817-9936d others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894016 | |||||
| chrX:107894196
|
C | CT | 5 | a0001c0001t0001g0086a0001c0001t0002g0056a0001c0002t0002g0136others(2): Show | 5 | NA18944.hp1 NA18945.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-9751dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894196 | |||||
| chrX:107894219
|
A | G | 1 | a0001c0001t0005g0018 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.817-9739A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894219 | ||||||
| chrX:107894765
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.817-9193C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894765 | ||||||
| chrX:107894828
|
A | AGT | 6 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0134others(3): Show | 6 | HG01071.hp1 HG01255.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-9094_817-9093d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894828 | |||||
| chrX:107894828
|
AGT | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(13): Show | 16 | HG00735.hp2 HG01516.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.817-9094_817-9093d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894828 | |||||
| chrX:107894860
|
T | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-9098T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894860 | ||||||
| chrX:107894861
|
G | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-9097G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894861 | ||||||
| chrX:107894862
|
T | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-9096T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894862 | ||||||
| chrX:107894863
|
G | GAA | 9 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-9095_817-9094i others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894863 | ||||||
| chrX:107894864
|
T | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(15): Show | 18 | HG00738.hp1 HG00741.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.817-9094T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894864 | ||||||
| chrX:107894864
|
T | TGTGAAA | 5 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0064others(2): Show | 5 | HG00280.hp1 HG01516.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-9093_817-9092i others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | |||||
| chrX:107894864
|
T | TGTGTGAA others(1): Show |
57 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0033others(54): Show | 57 | HG00140.hp1 HG00642.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.817-9093_817-9092i others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | |||||
| chrX:107894864
|
T | TGTGTGTG others(3): Show |
24 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0057others(21): Show | 24 | HG01069.hp1 HG01071.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.817-9093_817-9092i others(12): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | |||||
| chrX:107894864
|
T | TGTGTGTG others(5): Show |
6 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0043others(3): Show | 6 | HG00621.hp1 HG01109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-9093_817-9092i others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | |||||
| chrX:107894864
|
T | TGTGTGTG others(9): Show |
2 | a0001c0001t0003g0012a0001c0001t0003g0177 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.817-9093_817-9092i others(18): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894864 | |||||
| chrX:107894867
|
A | AAGAG | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0066others(5): Show | 8 | HG01258.hp1 HG02486.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.817-9075_817-9072d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894867 | |||||
| chrX:107894867
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0029others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.817-9091A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894867 | ||||||
| chrX:107894867
|
AAGAG | A | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.817-9075_817-9072d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107894867 | |||||
| chrX:107894912
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-9046A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107894912 | ||||||
| chrX:107895004
|
CT | C | 1 | a0001c0001t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.817-8949delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107895004 | |||||
| chrX:107895030
|
A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-8928A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895030 | ||||||
| chrX:107895215
|
T | TG | 19 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(16): Show | 19 | HG01516.hp2 HG02258.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.817-8733dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107895215 | |||||
| chrX:107895215
|
TG | T | 1 | a0001c0001t0001g0104 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.817-8733delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107895215 | |||||
| chrX:107895221
|
G | GC | 2 | a0001c0001t0003g0012a0001c0001t0003g0126 | 2 | HG01109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.817-8737_817-8736i others(3): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895221 | ||||||
| chrX:107895224
|
G | T | 1 | a0001c0001t0003g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.817-8734G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895224 | ||||||
| chrX:107895303
|
TC | T | 1 | a0001c0001t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.817-8649delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107895303 | |||||
| chrX:107895304
|
C | A | 32 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0046others(29): Show | 32 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.817-8654C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895304 | ||||||
| chrX:107895480
|
C | T | 10 | a0001c0001t0001g0165a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-8478C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895480 | ||||||
| chrX:107895543
|
G | A | 1 | a0001c0001t0008g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.817-8415G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895543 | ||||||
| chrX:107895787
|
A | G | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | NA18966.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.817-8171A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107895787 | ||||||
| chrX:107896097
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.817-7861G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896097 | ||||||
| chrX:107896238
|
C | T | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-7720C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896238 | ||||||
| chrX:107896408
|
G | A | 4 | a0001c0001t0002g0056a0001c0002t0002g0136a0001c0002t0002g0141others(1): Show | 4 | NA18944.hp1 NA18945.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-7550G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896408 | ||||||
| chrX:107896584
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-7374A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896584 | ||||||
| chrX:107896800
|
CCT | C | 2 | a0001c0001t0002g0132a0001c0001t0014g0171 | 2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.817-7146_817-7145d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107896800 | |||||
| chrX:107896812
|
T | A | 1 | a0001c0002t0002g0140 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.817-7146T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896812 | ||||||
| chrX:107896812
|
T | TCA | 6 | a0001c0001t0001g0165a0001c0002t0001g0154a0001c0002t0001g0155others(3): Show | 6 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-7128_817-7127d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107896812 | |||||
| chrX:107896814
|
A | T | 2 | a0001c0001t0001g0065a0001c0001t0005g0020 | 2 | HG03130.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.817-7144A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896814 | ||||||
| chrX:107896832
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.817-7126G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896832 | ||||||
| chrX:107896904
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-7054T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107896904 | ||||||
| chrX:107897319
|
A | T | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-6639A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107897319 | ||||||
| chrX:107897627
|
G | C | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.817-6331G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107897627 | ||||||
| chrX:107898001
|
C | CT | 3 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024 | 3 | HG01243.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.817-5951dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107898001 | |||||
| chrX:107898022
|
C | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-5936C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898022 | ||||||
| chrX:107898327
|
G | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.817-5631G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898327 | ||||||
| chrX:107898396
|
C | T | 2 | a0002c0003t0002g0161a0002c0003t0002g0162 | 2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.817-5562C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898396 | ||||||
| chrX:107898528
|
AT | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0100others(2): Show | 5 | HG01074.hp1 HG01433.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-5428delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107898528 | |||||
| chrX:107898916
|
T | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-5042T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898916 | ||||||
| chrX:107898967
|
T | C | 49 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0038others(46): Show | 49 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.817-4991T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107898967 | ||||||
| chrX:107899097
|
T | C | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.817-4861T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899097 | ||||||
| chrX:107899162
|
T | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0134 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.817-4796T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899162 | ||||||
| chrX:107899176
|
T | TC | 4 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-4777dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899176 | |||||
| chrX:107899176
|
T | TCC | 1 | a0001c0002t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.817-4778_817-4777d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899176 | |||||
| chrX:107899182
|
T | C | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-4776T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899182 | ||||||
| chrX:107899182
|
T | TC | 22 | a0001c0001t0001g0005a0001c0001t0001g0034a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp1 HG01192.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.817-4766dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899182 | |||||
| chrX:107899182
|
T | TCC | 5 | a0001c0001t0005g0027a0001c0001t0005g0028a0001c0001t0006g0023others(2): Show | 5 | HG02886.hp2 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-4767_817-4766d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899182 | |||||
| chrX:107899182
|
T | TCCC | 7 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(4): Show | 7 | HG02647.hp1 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-4768_817-4766d others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899182 | |||||
| chrX:107899182
|
T | TCCCCC | 1 | a0001c0001t0005g0020 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.817-4770_817-4766d others(7): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899182 | |||||
| chrX:107899182
|
TC | T | 1 | a0001c0001t0007g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.817-4766delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899182 | |||||
| chrX:107899193
|
A | C | 1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.817-4765A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899193 | ||||||
| chrX:107899457
|
G | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-4501G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899457 | ||||||
| chrX:107899741
|
A | AT | 11 | a0001c0001t0001g0086a0001c0001t0002g0178a0001c0001t0012g0173others(8): Show | 11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.817-4209dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899741 | |||||
| chrX:107899796
|
G | A | 1 | a0001c0002t0001g0146 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.817-4162G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899796 | ||||||
| chrX:107899948
|
G | A | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.817-4010G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107899948 | ||||||
| chrX:107899998
|
A | AG | 1 | a0001c0001t0001g0029 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.817-3959dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107899998 | |||||
| chrX:107900187
|
A | C | 2 | a0001c0001t0002g0132a0001c0001t0014g0171 | 2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.817-3771A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107900187 | ||||||
| chrX:107900699
|
TAA | T | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.817-3258_817-3257d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107900699 | ||||||
| chrX:107901046
|
A | AT | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-2910dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107901046 | |||||
| chrX:107901105
|
C | T | 1 | a0001c0001t0004g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.817-2853C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901105 | ||||||
| chrX:107901286
|
A | AG | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-2670dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107901286 | |||||
| chrX:107901328
|
AAGTAGCA others(8): Show |
A | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817-2629_817-2615d others(17): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901328 | ||||||
| chrX:107901378
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.817-2580G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901378 | ||||||
| chrX:107901396
|
G | GA | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-2558dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107901396 | |||||
| chrX:107901423
|
G | A | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-2535G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901423 | ||||||
| chrX:107901487
|
A | C | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-2471A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107901487 | ||||||
| chrX:107902071
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-1887C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902071 | ||||||
| chrX:107902166
|
A | AG | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1790dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902166 | |||||
| chrX:107902177
|
T | TCG | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1780_817-1779d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902177 | |||||
| chrX:107902300
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-1658T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902300 | ||||||
| chrX:107902322
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-1636C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902322 | ||||||
| chrX:107902506
|
TG | T | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1450delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902506 | |||||
| chrX:107902553
|
G | GC | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1402dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902553 | |||||
| chrX:107902594
|
GCA | G | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1363_817-1362d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902594 | ||||||
| chrX:107902602
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-1356C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902602 | ||||||
| chrX:107902603
|
A | AAC | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1355_817-1354i others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902603 | ||||||
| chrX:107902610
|
A | ATT | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1346_817-1345d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902610 | |||||
| chrX:107902636
|
T | TTAGCC | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1321_817-1317d others(7): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902636 | |||||
| chrX:107902755
|
G | GC | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1200dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902755 | |||||
| chrX:107902936
|
G | GCA | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-1021_817-1020i others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902936 | |||||
| chrX:107902988
|
G | GC | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-970_817-969ins others(1): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107902988 | ||||||
| chrX:107902993
|
T | TA | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-964dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107902993 | |||||
| chrX:107903048
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.817-910A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107903048 | ||||||
| chrX:107903308
|
G | GA | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-646dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903308 | |||||
| chrX:107903325
|
G | GT | 35 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0002g0006others(32): Show | 35 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.817-620dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903325 | |||||
| chrX:107903325
|
G | GTT | 1 | a0001c0006t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.817-621_817-620dup others(2): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903325 | |||||
| chrX:107903325
|
GT | G | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-620delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903325 | |||||
| chrX:107903379
|
G | C | 10 | a0001c0001t0002g0178a0001c0001t0012g0173a0002c0003t0002g0138others(7): Show | 10 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-579G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107903379 | ||||||
| chrX:107903492
|
A | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-466A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | chrX | 107903492 | ||||||
| chrX:107903505
|
AAAATTAG others(8): Show |
A | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.817-450_817-436del others(15): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903505 | |||||
| chrX:107903567
|
G | GT | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-389dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903567 | |||||
| chrX:107903700
|
G | GC | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-253dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903700 | |||||
| chrX:107903821
|
AC | A | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.817-134delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 107903821 | |||||
| chrX:107904072
|
C | T | 2 | a0001c0001t0008g0013a0001c0001t0008g0014 | 2 | HG02630.hp1 HG02818.hp2 |
splice_region_variant&intron_variant | LOW | c.924+7C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904072 | ||||||
| chrX:107904132
|
A | G | 3 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010 | 3 | HG02723.hp1 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.924+67A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904132 | ||||||
| chrX:107904229
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.924+164C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904229 | ||||||
| chrX:107904318
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.924+253A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904318 | ||||||
| chrX:107904466
|
G | GT | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.924+404dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 107904466 | |||||
| chrX:107904526
|
T | TG | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.924+464dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 107904526 | |||||
| chrX:107904601
|
AAACCAGA others(4): Show |
A | 1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.924+537_924+547del others(11): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | chrX | 107904601 | ||||||
| chrX:107904658
|
A | AG | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.924+595dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 107904658 | |||||
| chrX:107904963
|
AT | A | 1 | a0001c0001t0008g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.925-512delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 107904963 | |||||
| chrX:107905095
|
C | CA | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.925-380dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 107905095 | |||||
| chrX:107905170
|
T | TA | 1 | a0001c0001t0008g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.925-306dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 107905170 | |||||
| chrX:107905173
|
T | TG | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.925-302dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 107905173 | |||||
| chrX:107905458
|
C | CT | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.925-16dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chrX | 107905458 | |||||
| chrX:107905665
|
G | GA | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+43dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107905665 | |||||
| chrX:107905813
|
C | CAGCTCTT others(12): Show |
1 | a0001c0001t0005g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1073+188_1073+206d others(21): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107905813 | |||||
| chrX:107905887
|
G | GT | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+265dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107905887 | |||||
| chrX:107906047
|
A | AC | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+425dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906047 | |||||
| chrX:107906185
|
C | CA | 2 | a0001c0001t0001g0093a0002c0003t0002g0170 | 2 | HG00735.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1073+566dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906185 | |||||
| chrX:107906201
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1073+575T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906201 | ||||||
| chrX:107906413
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+790delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906413 | |||||
| chrX:107906416
|
T | TA | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+792dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906416 | |||||
| chrX:107906421
|
TC | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+799delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906421 | |||||
| chrX:107906475
|
TG | T | 1 | a0001c0001t0013g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1073+851delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906475 | |||||
| chrX:107906544
|
G | GT | 1 | a0001c0001t0003g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1073+923dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906544 | |||||
| chrX:107906557
|
C | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.1073+931C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906557 | ||||||
| chrX:107906648
|
C | G | 1 | a0001c0001t0013g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1073+1022C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906648 | ||||||
| chrX:107906649
|
G | C | 1 | a0001c0001t0013g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1073+1023G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906649 | ||||||
| chrX:107906650
|
A | ATCTTGGC others(13): Show |
1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+1026_1073+104 others(24): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906650 | |||||
| chrX:107906675
|
TC | T | 1 | a0001c0001t0008g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1073+1052delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906675 | |||||
| chrX:107906694
|
T | TC | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+1070dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906694 | |||||
| chrX:107906704
|
GC | G | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+1080delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906704 | |||||
| chrX:107906738
|
AC | A | 1 | a0001c0001t0008g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1073+1114delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906738 | |||||
| chrX:107906841
|
C | CTCCCAAA others(18): Show |
1 | a0001c0001t0001g0084 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1073+1217_1073+124 others(29): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906841 | |||||
| chrX:107906866
|
G | A | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+1240G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906866 | ||||||
| chrX:107906883
|
GC | G | 1 | a0001c0001t0013g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1073+1259delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906883 | |||||
| chrX:107906893
|
C | CT | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+1274dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906893 | |||||
| chrX:107906893
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+1274delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906893 | |||||
| chrX:107906932
|
A | AG | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1073+1307dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906932 | |||||
| chrX:107906943
|
GC | G | 1 | a0001c0001t0013g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1073+1319delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906943 | |||||
| chrX:107906963
|
TC | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+1339delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906963 | |||||
| chrX:107906984
|
TGTCTTCG others(8): Show |
T | 1 | a0001c0001t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1073+1359_1073+137 others(19): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906984 | ||||||
| chrX:107906987
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+1363delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107906987 | |||||
| chrX:107906990
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1073+1364C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107906990 | ||||||
| chrX:107907037
|
T | C | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+1411T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907037 | ||||||
| chrX:107907048
|
CA | C | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+1424delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907048 | |||||
| chrX:107907062
|
CCCTTG | C | 1 | a0001c0001t0005g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1073+1439_1073+144 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907062 | |||||
| chrX:107907125
|
C | CT | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+1504dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907125 | |||||
| chrX:107907130
|
TC | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+1506delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907130 | |||||
| chrX:107907189
|
T | TG | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+1565dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907189 | |||||
| chrX:107907255
|
T | TC | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+1631dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907255 | |||||
| chrX:107907257
|
C | T | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+1631C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907257 | ||||||
| chrX:107907282
|
CT | C | 1 | a0001c0001t0001g0029 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1073+1661delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907282 | |||||
| chrX:107907287
|
TA | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+1663delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907287 | |||||
| chrX:107907354
|
T | TC | 1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+1728_1073+172 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907354 | ||||||
| chrX:107907383
|
AT | A | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+1761delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907383 | |||||
| chrX:107907429
|
TATCAA | T | 1 | a0001c0001t0001g0055 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1073+1805_1073+180 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907429 | |||||
| chrX:107907475
|
CTTCCT | C | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+1851_1073+185 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907475 | |||||
| chrX:107907543
|
A | G | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1073+1917A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907543 | ||||||
| chrX:107907581
|
T | TC | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+1957dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907581 | |||||
| chrX:107907588
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+1962T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907588 | ||||||
| chrX:107907595
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073+1969A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907595 | ||||||
| chrX:107907627
|
C | CA | 5 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073+2008dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907627 | |||||
| chrX:107907690
|
T | TC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+2067dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907690 | |||||
| chrX:107907690
|
TC | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2067delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907690 | |||||
| chrX:107907731
|
A | AC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+2109dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907731 | |||||
| chrX:107907750
|
G | GA | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+2127dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907750 | |||||
| chrX:107907831
|
A | G | 1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1073+2205A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907831 | ||||||
| chrX:107907887
|
A | T | 10 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(7): Show | 10 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1073+2261A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107907887 | ||||||
| chrX:107907950
|
CA | C | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+2331delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907950 | |||||
| chrX:107907965
|
AG | A | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2341delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107907965 | |||||
| chrX:107908057
|
GGCACAGG others(3): Show |
G | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1073+2433_1073+244 others(14): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908057 | |||||
| chrX:107908085
|
T | TC | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073+2460dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908085 | |||||
| chrX:107908117
|
GC | G | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+2493delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908117 | |||||
| chrX:107908143
|
GT | G | 2 | a0001c0001t0001g0086a0004c0004t0001g0110 | 2 | NA18994.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1073+2522delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908143 | |||||
| chrX:107908161
|
T | TG | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1073+2535_1073+253 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908161 | ||||||
| chrX:107908188
|
TG | T | 1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+2564delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908188 | |||||
| chrX:107908193
|
G | GT | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1073+2571dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908193 | |||||
| chrX:107908199
|
AT | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+2580delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908199 | |||||
| chrX:107908207
|
CA | C | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2583delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908207 | |||||
| chrX:107908214
|
A | AG | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+2589dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908214 | |||||
| chrX:107908239
|
AT | A | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2616delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908239 | |||||
| chrX:107908256
|
G | GCCACTAC others(4): Show |
1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1073+2631_1073+264 others(15): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908256 | |||||
| chrX:107908274
|
AT | A | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2653delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908274 | |||||
| chrX:107908324
|
AT | A | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+2701delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908324 | |||||
| chrX:107908365
|
AT | A | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2744delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908365 | |||||
| chrX:107908381
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2760delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908381 | |||||
| chrX:107908387
|
A | AT | 2 | a0001c0001t0001g0045a0004c0004t0001g0110 | 2 | HG01928.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1073+2768dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908387 | |||||
| chrX:107908426
|
A | AT | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+2804dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908426 | |||||
| chrX:107908442
|
AT | A | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+2818delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908442 | |||||
| chrX:107908478
|
G | GT | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2853dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908478 | |||||
| chrX:107908534
|
A | AC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+2909dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908534 | |||||
| chrX:107908541
|
T | TG | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+2915_1073+291 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908541 | ||||||
| chrX:107908543
|
T | TG | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+2917_1073+291 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908543 | ||||||
| chrX:107908552
|
A | AAT | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2926_1073+292 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908552 | ||||||
| chrX:107908553
|
T | C | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+2927T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908553 | ||||||
| chrX:107908553
|
T | G | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+2927T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908553 | ||||||
| chrX:107908554
|
T | TA | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+2928_1073+292 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908554 | ||||||
| chrX:107908560
|
C | CA | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+2934_1073+293 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908560 | ||||||
| chrX:107908564
|
T | TA | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1073+2944dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908564 | |||||
| chrX:107908564
|
TA | T | 3 | a0001c0001t0001g0086a0002c0003t0002g0164a0005c0005t0001g0103 | 3 | HG04204.hp1 NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1073+2944delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908564 | |||||
| chrX:107908566
|
A | AAAAATGT others(12): Show |
1 | a0001c0001t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1073+2943_1073+296 others(23): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908566 | |||||
| chrX:107908625
|
C | CA | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3000dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908625 | |||||
| chrX:107908667
|
C | CA | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+3042dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908667 | |||||
| chrX:107908672
|
TG | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3049delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908672 | |||||
| chrX:107908682
|
A | G | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+3056A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908682 | ||||||
| chrX:107908696
|
T | TA | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 79 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1073+3088dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908696 | |||||
| chrX:107908696
|
T | TAA | 20 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0002g0038others(17): Show | 20 | HG01243.hp1 HG02486.hp1 HG02622.hp2 others(17): Show |
intron_variant | MODIFIER | c.1073+3087_1073+308 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908696 | |||||
| chrX:107908696
|
T | TAAA | 2 | a0001c0001t0001g0121a0001c0001t0005g0016 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1073+3086_1073+308 others(7): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908696 | |||||
| chrX:107908696
|
TA | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0079a0001c0001t0001g0080others(2): Show | 5 | HG02015.hp1 NA18962.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+3088delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908696 | |||||
| chrX:107908696
|
TAA | T | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1073+3087_1073+308 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908696 | |||||
| chrX:107908715
|
G | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+3089G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107908715 | ||||||
| chrX:107908754
|
TG | T | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+3131delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908754 | |||||
| chrX:107908799
|
G | GT | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+3174dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908799 | |||||
| chrX:107908836
|
T | TG | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+3213dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908836 | |||||
| chrX:107908863
|
GA | G | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3241delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908863 | |||||
| chrX:107908868
|
C | CA | 1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+3249dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908868 | |||||
| chrX:107908868
|
CA | C | 1 | a0001c0001t0001g0080 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1073+3249delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908868 | |||||
| chrX:107908897
|
C | CT | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1073+3274dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908897 | |||||
| chrX:107908897
|
CT | C | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1073+3274delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908897 | |||||
| chrX:107908921
|
T | TA | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+3299dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908921 | |||||
| chrX:107908940
|
T | TC | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3316dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908940 | |||||
| chrX:107908960
|
T | TA | 1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+3335dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908960 | |||||
| chrX:107908975
|
T | TG | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+3352dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908975 | |||||
| chrX:107908982
|
G | GT | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3359dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107908982 | |||||
| chrX:107909041
|
T | TC | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3416dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909041 | |||||
| chrX:107909048
|
A | AT | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+3428dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909048 | |||||
| chrX:107909087
|
G | A | 3 | a0001c0001t0006g0022a0001c0001t0006g0023a0001c0001t0006g0024 | 3 | HG01243.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1073+3461G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909087 | ||||||
| chrX:107909096
|
T | TA | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+3471dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909096 | |||||
| chrX:107909106
|
TATTCCTA others(28): Show |
T | 1 | a0001c0001t0001g0111 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1073+3482_1073+351 others(39): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909106 | |||||
| chrX:107909114
|
T | TA | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+3491dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909114 | |||||
| chrX:107909179
|
G | GTCTTGGT others(5): Show |
1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+3554_1073+356 others(16): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909179 | |||||
| chrX:107909234
|
A | AT | 1 | a0001c0001t0001g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1073+3613dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909234 | |||||
| chrX:107909254
|
C | CA | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+3632dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909254 | |||||
| chrX:107909254
|
C | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+3628C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909254 | ||||||
| chrX:107909275
|
A | AT | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3651dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909275 | |||||
| chrX:107909278
|
C | CAGGT | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+3652_1073+365 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909278 | ||||||
| chrX:107909280
|
A | C | 1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+3654A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909280 | ||||||
| chrX:107909308
|
G | GT | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+3685dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909308 | |||||
| chrX:107909311
|
T | TA | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+3686dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909311 | |||||
| chrX:107909315
|
TG | T | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073+3691delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909315 | |||||
| chrX:107909318
|
T | TA | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+3693dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909318 | |||||
| chrX:107909321
|
G | GA | 2 | a0001c0001t0001g0086a0002c0003t0002g0164 | 2 | HG04204.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1073+3697dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909321 | |||||
| chrX:107909326
|
C | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 95 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.1073+3700C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909326 | ||||||
| chrX:107909329
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3703_1073+370 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909329 | ||||||
| chrX:107909336
|
C | CT | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1073+3711dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909336 | |||||
| chrX:107909352
|
AC | A | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+3728delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909352 | |||||
| chrX:107909355
|
AG | A | 3 | a0001c0001t0001g0099a0004c0004t0001g0110a0005c0005t0001g0103 | 3 | HG01884.hp1 NA19062.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1073+3732delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909355 | |||||
| chrX:107909371
|
T | C | 2 | a0001c0001t0009g0026a0001c0002t0009g0176 | 2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1073+3745T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909371 | ||||||
| chrX:107909379
|
TG | T | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+3756delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909379 | |||||
| chrX:107909383
|
TG | T | 2 | a0001c0001t0001g0086a0001c0001t0003g0015 | 2 | HG03098.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1073+3759delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909383 | |||||
| chrX:107909391
|
TC | T | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+3769delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909391 | |||||
| chrX:107909463
|
G | GA | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+3839dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909463 | |||||
| chrX:107909500
|
C | CT | 2 | a0001c0001t0001g0005a0002c0003t0002g0164 | 2 | HG02145.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1073+3875dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909500 | |||||
| chrX:107909506
|
C | CT | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073+3881dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909506 | |||||
| chrX:107909534
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1073+3908G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909534 | ||||||
| chrX:107909557
|
T | TC | 1 | a0001c0001t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1073+3932dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909557 | |||||
| chrX:107909570
|
AG | A | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+3947delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909570 | |||||
| chrX:107909589
|
GC | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0099 | 2 | HG01884.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1073+3965delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909589 | |||||
| chrX:107909604
|
TC | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+3980delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909604 | |||||
| chrX:107909652
|
G | GT | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1073+4029dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909652 | |||||
| chrX:107909660
|
A | AG | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+4035dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909660 | |||||
| chrX:107909672
|
TG | T | 2 | a0001c0001t0001g0045a0005c0005t0001g0103 | 2 | HG01928.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1073+4049delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909672 | |||||
| chrX:107909687
|
C | CA | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+4063dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909687 | |||||
| chrX:107909693
|
CT | C | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073+4072delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909693 | |||||
| chrX:107909709
|
AT | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4086delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909709 | |||||
| chrX:107909713
|
CA | C | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+4089delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909713 | |||||
| chrX:107909738
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073+4112T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107909738 | ||||||
| chrX:107909835
|
TA | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4211delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909835 | |||||
| chrX:107909847
|
TA | T | 2 | a0001c0001t0002g0038a0002c0003t0002g0160 | 2 | HG01515.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1073+4225delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909847 | |||||
| chrX:107909860
|
CT | C | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4236delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909860 | |||||
| chrX:107909881
|
CT | C | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4259delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909881 | |||||
| chrX:107909915
|
TG | T | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1073+4292delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909915 | |||||
| chrX:107909931
|
G | GT | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4309dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909931 | |||||
| chrX:107909966
|
C | CA | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4343dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909966 | |||||
| chrX:107909966
|
CA | C | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+4343delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909966 | |||||
| chrX:107909983
|
TC | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4359delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909983 | |||||
| chrX:107909997
|
AT | A | 3 | a0001c0001t0001g0099a0002c0003t0002g0160a0002c0003t0002g0164 | 3 | HG01515.hp1 HG01884.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1073+4377delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107909997 | |||||
| chrX:107910011
|
G | GC | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4387dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910011 | |||||
| chrX:107910020
|
A | AT | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4397dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910020 | |||||
| chrX:107910027
|
CT | C | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+4405delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910027 | |||||
| chrX:107910036
|
AT | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0099 | 2 | HG01884.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1073+4414delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910036 | |||||
| chrX:107910082
|
G | GC | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+4457dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910082 | |||||
| chrX:107910082
|
G | GCACAA | 1 | a0001c0002t0002g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1073+4459_1073+446 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910082 | |||||
| chrX:107910090
|
G | GA | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4465dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910090 | |||||
| chrX:107910097
|
GA | G | 1 | a0001c0001t0002g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1073+4474delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910097 | |||||
| chrX:107910104
|
A | T | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4478A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910104 | ||||||
| chrX:107910116
|
TA | T | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4492delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910116 | |||||
| chrX:107910125
|
CT | C | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+4502delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910125 | |||||
| chrX:107910130
|
T | TA | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4505dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910130 | |||||
| chrX:107910131
|
A | AC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4508dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910131 | |||||
| chrX:107910134
|
CT | C | 2 | a0001c0001t0001g0005a0004c0004t0001g0110 | 2 | HG02145.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1073+4511delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910134 | |||||
| chrX:107910144
|
CA | C | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+4520delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910144 | |||||
| chrX:107910148
|
T | TC | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1073+4526dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910148 | |||||
| chrX:107910148
|
TC | T | 3 | a0001c0001t0001g0073a0001c0002t0001g0157a0005c0005t0001g0103 | 3 | HG02970.hp1 NA19082.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1073+4526delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910148 | |||||
| chrX:107910153
|
A | AT | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4529dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910153 | |||||
| chrX:107910155
|
TC | T | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+4532delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910155 | |||||
| chrX:107910168
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1073+4542C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910168 | ||||||
| chrX:107910176
|
AGTAACC | A | 1 | a0001c0001t0003g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1073+4551_1073+455 others(10): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910176 | ||||||
| chrX:107910198
|
A | AT | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4575dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910198 | |||||
| chrX:107910238
|
G | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+4612G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910238 | ||||||
| chrX:107910247
|
T | TG | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+4623dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910247 | |||||
| chrX:107910257
|
CT | C | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+4634delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910257 | |||||
| chrX:107910274
|
AT | A | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+4652delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910274 | |||||
| chrX:107910302
|
C | CA | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4677dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910302 | |||||
| chrX:107910310
|
C | CT | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+4685dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910310 | |||||
| chrX:107910325
|
GGAT | G | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+4700_1073+470 others(7): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910325 | ||||||
| chrX:107910330
|
T | TC | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1073+4706dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910330 | |||||
| chrX:107910349
|
G | GA | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4726dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910349 | |||||
| chrX:107910362
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1073+4736T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910362 | ||||||
| chrX:107910376
|
C | CA | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4751dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910376 | |||||
| chrX:107910379
|
AT | A | 2 | a0001c0002t0001g0157a0004c0004t0001g0110 | 2 | HG02970.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1073+4757delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910379 | |||||
| chrX:107910384
|
CT | C | 2 | a0001c0001t0001g0106a0001c0002t0002g0141 | 2 | HG04115.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1073+4761delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910384 | |||||
| chrX:107910407
|
GA | G | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4784delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910407 | |||||
| chrX:107910408
|
A | AT | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+4782_1073+478 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910408 | ||||||
| chrX:107910411
|
C | CCCT | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+4785_1073+478 others(7): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910411 | ||||||
| chrX:107910431
|
TG | T | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1073+4807delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910431 | |||||
| chrX:107910443
|
A | AT | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+4818dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910443 | |||||
| chrX:107910446
|
A | AC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4820_1073+482 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910446 | ||||||
| chrX:107910448
|
G | GC | 1 | a0001c0001t0001g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1073+4823dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910448 | |||||
| chrX:107910461
|
TG | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+4838delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910461 | |||||
| chrX:107910474
|
AT | A | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+4851delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910474 | |||||
| chrX:107910487
|
AT | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1073+4863delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910487 | |||||
| chrX:107910513
|
ACTGAC | A | 1 | a0001c0001t0001g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1073+4888_1073+489 others(9): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910513 | ||||||
| chrX:107910520
|
AG | A | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1073+4895delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910520 | ||||||
| chrX:107910522
|
TG | T | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4899delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910522 | |||||
| chrX:107910535
|
TC | T | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+4911delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910535 | |||||
| chrX:107910545
|
G | GT | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1073+4921dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910545 | |||||
| chrX:107910550
|
AT | A | 2 | a0001c0001t0001g0085a0001c0001t0010g0123 | 2 | HG02027.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1073+4929delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910550 | |||||
| chrX:107910557
|
G | GT | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4937dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910557 | |||||
| chrX:107910557
|
GT | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0117a0001c0002t0002g0136 | 3 | HG00558.hp2 NA18944.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1073+4937delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910557 | |||||
| chrX:107910565
|
A | AG | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+4941dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910565 | |||||
| chrX:107910565
|
AG | A | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+4941delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910565 | |||||
| chrX:107910569
|
A | ACT | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1073+4944_1073+494 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910569 | |||||
| chrX:107910580
|
G | GT | 3 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0093 | 3 | HG00735.hp1 NA18994.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1073+4960dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910580 | |||||
| chrX:107910580
|
GT | G | 1 | a0001c0001t0001g0039 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1073+4960delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910580 | |||||
| chrX:107910594
|
C | CT | 3 | a0001c0001t0001g0106a0002c0003t0002g0138a0002c0003t0002g0164 | 3 | HG01516.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1073+4969dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910594 | |||||
| chrX:107910602
|
AT | A | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+4979delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910602 | |||||
| chrX:107910610
|
TCC | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+4986_1073+498 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910610 | |||||
| chrX:107910612
|
C | CA | 1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+4986_1073+498 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910612 | ||||||
| chrX:107910618
|
AC | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+4993delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910618 | ||||||
| chrX:107910619
|
C | CA | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1073+4995dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910619 | |||||
| chrX:107910633
|
T | TC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+5010dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910633 | |||||
| chrX:107910636
|
CT | C | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+5014delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910636 | |||||
| chrX:107910648
|
T | TC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+5024dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910648 | |||||
| chrX:107910662
|
T | TA | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+5037dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910662 | |||||
| chrX:107910673
|
CT | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0047a0002c0003t0002g0164others(1): Show | 4 | HG02735.hp1 HG04204.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+5051delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910673 | |||||
| chrX:107910677
|
TA | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073+5053delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910677 | |||||
| chrX:107910680
|
TA | T | 2 | a0002c0003t0002g0164a0004c0004t0001g0110 | 2 | HG04204.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1073+5056delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910680 | |||||
| chrX:107910690
|
T | TTA | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1073+5064_1073+506 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910690 | ||||||
| chrX:107910694
|
A | AT | 2 | a0001c0001t0001g0117a0002c0003t0002g0138 | 2 | HG00558.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1073+5069dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910694 | |||||
| chrX:107910706
|
TA | T | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+5083delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910706 | |||||
| chrX:107910721
|
T | TG | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+5095_1073+509 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910721 | ||||||
| chrX:107910721
|
TA | T | 1 | a0001c0001t0001g0073 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1073+5097delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910721 | |||||
| chrX:107910727
|
A | AG | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1073+5102dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910727 | |||||
| chrX:107910728
|
G | GT | 4 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0004g0115others(1): Show | 4 | HG03540.hp1 NA19062.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+5107dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910728 | |||||
| chrX:107910728
|
GT | G | 1 | a0001c0002t0002g0136 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1073+5107delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910728 | |||||
| chrX:107910739
|
A | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073+5113A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910739 | ||||||
| chrX:107910753
|
T | TG | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+5128dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910753 | |||||
| chrX:107910754
|
G | GC | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1073+5130dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910754 | |||||
| chrX:107910767
|
A | AT | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1073+5145dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910767 | |||||
| chrX:107910767
|
A | ATTCTTTC others(271): Show |
1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+5143_1073+514 others(282): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910767 | |||||
| chrX:107910767
|
A | ATTTTCCT others(259): Show |
1 | a0001c0001t0001g0073 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(270): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910767 | |||||
| chrX:107910768
|
T | TTTTCCTT others(146): Show |
1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+5154_1073+515 others(157): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(297): Show |
1 | a0005c0005t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1073+5154_1073+515 others(308): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(277): Show |
1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+5154_1073+515 others(288): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(252): Show |
1 | a0001c0001t0001g0039 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1073+5159_1073+516 others(263): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(221): Show |
1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1073+5159_1073+516 others(232): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(324): Show |
1 | a0001c0001t0004g0098 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1073+5162_1073+516 others(335): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(292): Show |
1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1073+5164_1073+516 others(303): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(333): Show |
1 | a0001c0001t0001g0078 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1073+5182_1073+518 others(344): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(250): Show |
1 | a0001c0001t0001g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(261): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(168): Show |
1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(179): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(228): Show |
1 | a0001c0001t0004g0032 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(239): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(285): Show |
1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(296): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(153): Show |
1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(164): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(158): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0096 | 2 | HG01516.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(169): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(173): Show |
1 | a0001c0001t0001g0097 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(184): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(178): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0118 | 2 | HG00673.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(189): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(183): Show |
2 | a0001c0001t0001g0058a0001c0001t0001g0066 | 2 | HG01071.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(194): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(188): Show |
1 | a0001c0001t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(199): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(203): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0080others(1): Show | 4 | HG03688.hp1 NA18953.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(214): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(208): Show |
2 | a0001c0001t0001g0061a0001c0001t0001g0094 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(219): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(213): Show |
3 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0001g0125 | 3 | HG02622.hp1 HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(224): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(218): Show |
3 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0001g0082 | 3 | HG03704.hp1 NA18955.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(229): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(223): Show |
2 | a0001c0001t0001g0064a0001c0001t0001g0090 | 2 | HG00280.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(234): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(233): Show |
3 | a0001c0001t0001g0054a0001c0001t0001g0120a0001c0001t0001g0181 | 3 | HG02630.hp2 HG02976.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(244): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(238): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0060 | 2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(249): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(243): Show |
5 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0065others(2): Show | 5 | HG00738.hp1 HG02132.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(254): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(248): Show |
5 | a0001c0001t0001g0048a0001c0001t0001g0075a0001c0001t0001g0084others(2): Show | 5 | HG00642.hp1 HG02922.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(259): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(253): Show |
2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG00140.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(264): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(258): Show |
3 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0111 | 3 | HG00735.hp1 NA18961.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(269): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(350): Show |
1 | a0001c0001t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(361): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(263): Show |
2 | a0001c0001t0001g0029a0001c0001t0001g0104 | 2 | HG01099.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(274): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(268): Show |
4 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0055others(1): Show | 4 | HG01433.hp1 HG02040.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(279): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(283): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0095 | 2 | HG02602.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(294): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(288): Show |
1 | a0001c0001t0004g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(299): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(293): Show |
1 | a0001c0001t0001g0002 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(304): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(298): Show |
1 | a0001c0001t0001g0040 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(309): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(303): Show |
1 | a0001c0001t0001g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(314): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(308): Show |
1 | a0001c0001t0004g0115 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(319): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(333): Show |
1 | a0001c0001t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(344): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(343): Show |
1 | a0001c0001t0004g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(354): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(200): Show |
1 | a0001c0001t0001g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(211): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(229): Show |
1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(240): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(165): Show |
1 | a0001c0001t0002g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1074-5181_1074-518 others(176): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(129): Show |
1 | a0001c0002t0001g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074-5185_1074-518 others(140): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(229): Show |
1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073+5185_1073+518 others(240): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(172): Show |
1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1073+5181_1073+518 others(183): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(323): Show |
1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1073+5181_1073+518 others(334): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910768
|
T | TTTTCCTT others(217): Show |
1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1073+5165_1073+516 others(228): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910768 | |||||
| chrX:107910771
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1073+5145T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910771 | ||||||
| chrX:107910782
|
C | CT | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1073+5156_1073+515 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910782 | ||||||
| chrX:107910788
|
C | CTTTCCTT others(200): Show |
1 | a0001c0001t0001g0077 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1074-5175_1074-517 others(211): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910788 | |||||
| chrX:107910795
|
T | TTCCCTTT others(294): Show |
1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1073+5172_1073+517 others(305): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910795 | |||||
| chrX:107910796
|
TC | T | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1073+5172delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910796 | |||||
| chrX:107910797
|
C | CCTTTCCT others(352): Show |
1 | a0001c0001t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(363): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910797 | |||||
| chrX:107910797
|
C | CCTTTCCT others(176): Show |
1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1074-5185_1074-518 others(187): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910797 | |||||
| chrX:107910803
|
C | CTTTCCTT others(350): Show |
1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(361): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910803 | |||||
| chrX:107910807
|
C | CCTTTCCC others(281): Show |
1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1073+5187_1073+518 others(292): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910807 | |||||
| chrX:107910808
|
C | CT | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1073+5185dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910808 | |||||
| chrX:107910809
|
T | TTTCCTTT others(228): Show |
1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(239): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910809 | |||||
| chrX:107910833
|
CT | C | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-5166delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910833 | |||||
| chrX:107910834
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1074-5168T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910834 | ||||||
| chrX:107910834
|
T | TTCCTTTC others(274): Show |
1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-5167_1074-516 others(285): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910834 | |||||
| chrX:107910835
|
T | C | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-5167T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910835 | ||||||
| chrX:107910836
|
T | TCCTTTCC others(267): Show |
1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(278): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910836 | |||||
| chrX:107910836
|
T | TCTTTCCT others(294): Show |
1 | a0001c0001t0004g0116 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1074-5165_1074-516 others(305): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910836 | |||||
| chrX:107910837
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-5165C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910837 | ||||||
| chrX:107910838
|
C | CCTTCCCT others(209): Show |
1 | a0001c0001t0002g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1074-5162_1074-516 others(220): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910838 | |||||
| chrX:107910838
|
C | CT | 5 | a0001c0001t0001g0005a0001c0001t0002g0038a0001c0001t0002g0132others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCCT others(264): Show |
1 | a0001c0001t0002g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(275): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCCT others(244): Show |
1 | a0001c0001t0002g0053 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(255): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCCT others(214): Show |
1 | a0001c0001t0002g0006 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(225): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(239): Show |
1 | a0001c0002t0002g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(250): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(306): Show |
1 | a0001c0001t0002g0050 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(317): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(244): Show |
1 | a0001c0001t0002g0046 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(255): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(224): Show |
1 | a0001c0001t0002g0051 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(235): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(199): Show |
1 | a0001c0002t0002g0148 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(210): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(239): Show |
1 | a0001c0001t0002g0052 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(250): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(194): Show |
1 | a0001c0002t0002g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(205): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(169): Show |
1 | a0001c0002t0002g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(180): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(173): Show |
1 | a0001c0002t0002g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(184): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(193): Show |
1 | a0001c0002t0002g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(204): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(218): Show |
1 | a0002c0003t0002g0138 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(229): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(194): Show |
1 | a0001c0002t0002g0137 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(205): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(228): Show |
1 | a0001c0002t0002g0140 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(239): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(194): Show |
1 | a0001c0002t0002g0144 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(205): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(199): Show |
1 | a0001c0002t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(210): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(204): Show |
1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(215): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(174): Show |
2 | a0001c0001t0013g0114a0001c0002t0001g0146 | 2 | NA18975.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(185): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(269): Show |
1 | a0001c0002t0002g0147 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(280): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(229): Show |
1 | a0001c0001t0002g0091 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(240): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(225): Show |
1 | a0001c0006t0002g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(236): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(189): Show |
1 | a0001c0002t0002g0152 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(200): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(204): Show |
1 | a0001c0002t0002g0145 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(215): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(240): Show |
1 | a0001c0002t0002g0136 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(251): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(219): Show |
1 | a0001c0002t0002g0151 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(230): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(79): Show |
1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(90): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(119): Show |
3 | a0001c0001t0005g0028a0001c0001t0007g0167a0001c0001t0009g0026 | 3 | HG01106.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(130): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(124): Show |
1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(135): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(134): Show |
2 | a0001c0001t0005g0020a0001c0001t0014g0171 | 2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(145): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(139): Show |
3 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0168 | 3 | HG01884.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(150): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(144): Show |
1 | a0001c0001t0003g0012 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(155): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(149): Show |
5 | a0001c0001t0003g0177a0001c0001t0007g0169a0001c0001t0008g0013others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(160): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(169): Show |
1 | a0001c0001t0002g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(180): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(154): Show |
4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0005g0018others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(165): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(159): Show |
1 | a0002c0003t0002g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(170): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(159): Show |
3 | a0001c0001t0003g0015a0001c0001t0005g0016a0001c0001t0006g0024 | 3 | HG02886.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(170): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(248): Show |
1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(259): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(164): Show |
2 | a0001c0001t0001g0174a0001c0001t0003g0008 | 2 | HG02451.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(175): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(169): Show |
1 | a0002c0003t0002g0170 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(180): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(169): Show |
4 | a0001c0001t0001g0121a0001c0001t0005g0027a0001c0001t0006g0022others(1): Show | 4 | HG01243.hp1 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(180): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(174): Show |
3 | a0001c0001t0001g0124a0001c0001t0003g0007a0001c0002t0001g0172 | 3 | HG01891.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(185): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(179): Show |
1 | a0001c0002t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(190): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(184): Show |
1 | a0002c0003t0002g0161 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(195): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(183): Show |
1 | a0001c0001t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(194): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(184): Show |
3 | a0001c0001t0001g0175a0001c0001t0003g0011a0001c0002t0001g0156 | 3 | HG02717.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(195): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(189): Show |
2 | a0001c0001t0001g0004a0001c0001t0008g0134 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(200): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(199): Show |
1 | a0002c0003t0002g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(210): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(199): Show |
3 | a0001c0002t0006g0179a0001c0002t0006g0180a0001c0002t0009g0176 | 3 | HG02647.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(210): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(204): Show |
1 | a0001c0001t0001g0003 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(215): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(209): Show |
1 | a0001c0001t0003g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(220): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(219): Show |
2 | a0002c0003t0002g0163a0003c0007t0002g0131 | 2 | HG01168.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1074-5164_1074-516 others(230): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(229): Show |
1 | a0001c0001t0012g0173 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(240): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(224): Show |
1 | a0001c0001t0005g0017 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(235): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(234): Show |
1 | a0001c0001t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(245): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(239): Show |
1 | a0001c0001t0005g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(250): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(259): Show |
1 | a0001c0002t0002g0153 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(270): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(236): Show |
1 | a0002c0003t0002g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(247): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(194): Show |
1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(205): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | CTTTCCTT others(187): Show |
1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1074-5164_1074-516 others(198): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910838
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074-5164C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910838 | ||||||
| chrX:107910843
|
C | CT | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-5158dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910843 | |||||
| chrX:107910845
|
C | CT | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-5154dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910845 | |||||
| chrX:107910845
|
CT | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0119 | 2 | HG01952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1074-5154delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910845 | |||||
| chrX:107910850
|
T | TC | 2 | a0001c0001t0001g0072a0004c0004t0001g0110 | 2 | HG04228.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1074-5149dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910850 | |||||
| chrX:107910850
|
TC | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-5149delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910850 | |||||
| chrX:107910852
|
C | CT | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1074-5150_1074-514 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910852 | ||||||
| chrX:107910852
|
CCT | C | 2 | a0001c0001t0001g0117a0001c0001t0002g0038 | 2 | HG00558.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1074-5139_1074-513 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910852 | |||||
| chrX:107910855
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1074-5147C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910855 | ||||||
| chrX:107910868
|
CT | C | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1074-5132delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910868 | |||||
| chrX:107910871
|
CT | C | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-5128delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910871 | |||||
| chrX:107910890
|
G | GT | 1 | a0001c0001t0005g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1074-5110dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910890 | |||||
| chrX:107910893
|
G | GC | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-5106dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910893 | |||||
| chrX:107910897
|
A | AG | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-5103dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910897 | |||||
| chrX:107910914
|
CA | C | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-5087delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910914 | ||||||
| chrX:107910935
|
T | TC | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1074-5066dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910935 | |||||
| chrX:107910939
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 180 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.1074-5063T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910939 | ||||||
| chrX:107910940
|
G | GC | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1074-5060dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910940 | |||||
| chrX:107910943
|
TC | T | 2 | a0001c0001t0001g0030a0001c0001t0010g0123 | 2 | NA19043.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1074-5056delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910943 | |||||
| chrX:107910947
|
AG | A | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1074-5054delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910947 | ||||||
| chrX:107910971
|
A | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1074-5031A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910971 | ||||||
| chrX:107910979
|
TG | T | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1074-5021delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910979 | |||||
| chrX:107910986
|
TG | T | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1074-5013delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910986 | |||||
| chrX:107910990
|
A | AT | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-5012_1074-501 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910990 | ||||||
| chrX:107910995
|
AG | A | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1074-5005delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107910995 | |||||
| chrX:107910997
|
G | C | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-5005G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107910997 | ||||||
| chrX:107911011
|
G | GC | 1 | a0001c0001t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1074-4988dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911011 | |||||
| chrX:107911020
|
AT | A | 1 | a0001c0001t0001g0072 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1074-4978delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911020 | |||||
| chrX:107911024
|
TG | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4976delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911024 | |||||
| chrX:107911028
|
AT | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0047 | 2 | HG02735.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1074-4969delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911028 | |||||
| chrX:107911044
|
TG | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-4956delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911044 | |||||
| chrX:107911051
|
AC | A | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1074-4949delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911051 | |||||
| chrX:107911067
|
TG | T | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1074-4933delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911067 | |||||
| chrX:107911074
|
GA | G | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1074-4926delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911074 | |||||
| chrX:107911097
|
GC | G | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-4902delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911097 | |||||
| chrX:107911103
|
C | CA | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1074-4899_1074-489 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911103 | ||||||
| chrX:107911105
|
TG | T | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-4895delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911105 | |||||
| chrX:107911113
|
CA | C | 2 | a0001c0001t0001g0117a0001c0001t0002g0038 | 2 | HG00558.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1074-4886delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911113 | |||||
| chrX:107911117
|
G | A | 1 | a0001c0001t0011g0025 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1074-4885G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911117 | ||||||
| chrX:107911130
|
AG | A | 2 | a0001c0001t0001g0069a0005c0005t0001g0103 | 2 | NA19091.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1074-4870delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911130 | |||||
| chrX:107911134
|
G | GT | 1 | a0001c0001t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1074-4867dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911134 | |||||
| chrX:107911159
|
TG | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1074-4841delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911159 | |||||
| chrX:107911163
|
CT | C | 2 | a0001c0001t0001g0119a0001c0001t0010g0123 | 2 | HG01952.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1074-4834delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911163 | |||||
| chrX:107911176
|
AT | A | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4821delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911176 | |||||
| chrX:107911184
|
T | TG | 1 | a0001c0002t0002g0136 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1074-4815dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911184 | |||||
| chrX:107911200
|
CT | C | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-4799delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911200 | |||||
| chrX:107911233
|
TG | T | 2 | a0001c0001t0002g0132a0005c0005t0001g0103 | 2 | HG01891.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1074-4766delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911233 | |||||
| chrX:107911267
|
C | T | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-4735C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911267 | ||||||
| chrX:107911269
|
T | C | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-4733T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911269 | ||||||
| chrX:107911269
|
TC | T | 1 | a0001c0001t0010g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1074-4729delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911269 | |||||
| chrX:107911270
|
C | T | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-4732C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911270 | ||||||
| chrX:107911273
|
CT | C | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-4726delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911273 | |||||
| chrX:107911304
|
T | C | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-4698T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911304 | ||||||
| chrX:107911314
|
G | GA | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074-4686dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911314 | |||||
| chrX:107911323
|
G | GA | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-4678dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911323 | |||||
| chrX:107911334
|
CT | C | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-4661delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911334 | |||||
| chrX:107911347
|
AT | A | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4651delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911347 | |||||
| chrX:107911354
|
C | CT | 1 | a0002c0003t0002g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1074-4644dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911354 | |||||
| chrX:107911396
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1074-4606T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911396 | ||||||
| chrX:107911400
|
TC | T | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1074-4600delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911400 | |||||
| chrX:107911438
|
ATT | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-4562_1074-456 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911438 | |||||
| chrX:107911451
|
TA | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4549delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911451 | |||||
| chrX:107911473
|
TC | T | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1074-4527delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911473 | |||||
| chrX:107911488
|
C | CT | 3 | a0001c0001t0001g0086a0001c0001t0004g0116a0004c0004t0001g0110 | 3 | NA18994.hp1 NA19060.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1074-4508dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911488 | |||||
| chrX:107911488
|
CT | C | 1 | a0001c0001t0004g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1074-4508delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911488 | |||||
| chrX:107911503
|
G | GT | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1074-4494dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911503 | |||||
| chrX:107911503
|
GT | G | 2 | a0001c0001t0001g0119a0001c0001t0010g0123 | 2 | HG01952.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1074-4494delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911503 | |||||
| chrX:107911527
|
AT | A | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074-4472delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911527 | |||||
| chrX:107911555
|
AT | A | 3 | a0001c0001t0001g0081a0001c0001t0002g0038a0001c0002t0002g0136 | 3 | HG01261.hp1 NA18522.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1074-4442delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911555 | |||||
| chrX:107911560
|
TA | T | 2 | a0001c0001t0001g0181a0001c0001t0002g0056 | 2 | HG02630.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1074-4438delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911560 | |||||
| chrX:107911574
|
TA | T | 2 | a0001c0001t0001g0030a0001c0002t0002g0141 | 2 | NA19079.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1074-4425delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911574 | |||||
| chrX:107911590
|
T | TG | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1074-4409dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911590 | |||||
| chrX:107911590
|
TG | T | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1074-4409delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911590 | |||||
| chrX:107911606
|
TC | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4394delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911606 | |||||
| chrX:107911635
|
CT | C | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074-4363delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911635 | |||||
| chrX:107911653
|
C | CA | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4346dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911653 | |||||
| chrX:107911661
|
TG | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4339delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911661 | |||||
| chrX:107911683
|
CA | C | 1 | a0001c0001t0002g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1074-4318delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911683 | ||||||
| chrX:107911686
|
TA | T | 1 | a0001c0001t0001g0094 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1074-4312delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911686 | |||||
| chrX:107911697
|
TG | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0181 | 2 | HG02630.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1074-4303delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911697 | |||||
| chrX:107911722
|
AT | A | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074-4277delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911722 | |||||
| chrX:107911726
|
A | AT | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1074-4275dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911726 | |||||
| chrX:107911751
|
AT | A | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-4249delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911751 | |||||
| chrX:107911760
|
CG | C | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-4240delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911760 | |||||
| chrX:107911777
|
AT | A | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-4223delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911777 | |||||
| chrX:107911782
|
TG | T | 2 | a0001c0001t0001g0069a0002c0003t0002g0164 | 2 | HG04204.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1074-4218delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911782 | |||||
| chrX:107911819
|
T | TG | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-4180dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911819 | |||||
| chrX:107911829
|
TC | T | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4170delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911829 | |||||
| chrX:107911832
|
C | CG | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-4170_1074-416 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911832 | ||||||
| chrX:107911839
|
GA | G | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-4160delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911839 | |||||
| chrX:107911860
|
T | TA | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-4142_1074-414 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911860 | ||||||
| chrX:107911869
|
AG | A | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074-4129delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911869 | |||||
| chrX:107911908
|
AT | A | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074-4092delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911908 | |||||
| chrX:107911924
|
AG | A | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1074-4075delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911924 | |||||
| chrX:107911927
|
GA | G | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-4071delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911927 | |||||
| chrX:107911928
|
A | G | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-4074A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107911928 | ||||||
| chrX:107911942
|
G | GT | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-4056dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911942 | |||||
| chrX:107911942
|
GT | G | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074-4056delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911942 | |||||
| chrX:107911951
|
C | CT | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074-4050dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107911951 | |||||
| chrX:107912012
|
AG | A | 2 | a0001c0001t0001g0181a0004c0004t0001g0110 | 2 | HG02630.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1074-3987delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912012 | |||||
| chrX:107912017
|
AG | A | 1 | a0001c0001t0001g0073 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1074-3982delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912017 | |||||
| chrX:107912079
|
CA | C | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074-3921delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912079 | |||||
| chrX:107912089
|
TG | T | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-3911delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912089 | |||||
| chrX:107912117
|
CT | C | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3883delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912117 | |||||
| chrX:107912133
|
T | TC | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-3868dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912133 | |||||
| chrX:107912140
|
A | AC | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-3861dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912140 | |||||
| chrX:107912155
|
C | CA | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-3846dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912155 | |||||
| chrX:107912168
|
CT | C | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074-3831delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912168 | |||||
| chrX:107912176
|
CT | C | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-3824delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912176 | |||||
| chrX:107912198
|
C | CT | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-3800dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912198 | |||||
| chrX:107912209
|
TG | T | 1 | a0001c0001t0001g0073 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1074-3791delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912209 | |||||
| chrX:107912217
|
CT | C | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074-3781delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912217 | |||||
| chrX:107912235
|
C | CT | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3764dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912235 | |||||
| chrX:107912235
|
CT | C | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1074-3764delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912235 | |||||
| chrX:107912243
|
GT | G | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1074-3756delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912243 | |||||
| chrX:107912294
|
CA | C | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-3703delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912294 | |||||
| chrX:107912315
|
A | AG | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-3687_1074-368 others(5): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107912315 | ||||||
| chrX:107912346
|
A | AC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-3653dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912346 | |||||
| chrX:107912353
|
GA | G | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-3646delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912353 | |||||
| chrX:107912370
|
T | TACC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-3629_1074-362 others(7): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912370 | |||||
| chrX:107912375
|
C | CA | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1074-3626dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912375 | |||||
| chrX:107912376
|
AC | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3624delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912376 | |||||
| chrX:107912379
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1074-3623A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107912379 | ||||||
| chrX:107912382
|
G | GA | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3617dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912382 | |||||
| chrX:107912398
|
A | AGGTC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-3603_1074-360 others(8): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912398 | |||||
| chrX:107912405
|
CA | C | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1074-3594delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912405 | |||||
| chrX:107912437
|
C | CA | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3564dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912437 | |||||
| chrX:107912453
|
CT | C | 1 | a0001c0001t0001g0070 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-3547delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912453 | |||||
| chrX:107912455
|
T | TA | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3546dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912455 | |||||
| chrX:107912479
|
T | TC | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1074-3521dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912479 | |||||
| chrX:107912486
|
G | GA | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-3514dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912486 | |||||
| chrX:107912488
|
A | AC | 1 | a0001c0001t0008g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1074-3513dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912488 | |||||
| chrX:107912549
|
CT | C | 1 | a0001c0001t0001g0073 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1074-3450delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912549 | |||||
| chrX:107912556
|
GT | G | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-3441delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912556 | |||||
| chrX:107912562
|
G | GT | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-3436dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912562 | |||||
| chrX:107912761
|
AG | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3239delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912761 | |||||
| chrX:107912793
|
A | AC | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-3208dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912793 | |||||
| chrX:107912845
|
TC | T | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-3154delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912845 | |||||
| chrX:107912871
|
A | G | 2 | a0001c0002t0006g0179a0001c0002t0006g0180 | 2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1074-3131A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107912871 | ||||||
| chrX:107912896
|
G | GC | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-3104dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912896 | |||||
| chrX:107912905
|
A | AC | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3096dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912905 | |||||
| chrX:107912930
|
TG | T | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-3069delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912930 | |||||
| chrX:107912947
|
T | TC | 2 | a0001c0001t0001g0063a0001c0001t0001g0106 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1074-3051dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912947 | |||||
| chrX:107912963
|
AC | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-3037delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107912963 | |||||
| chrX:107913015
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1074-2987C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913015 | ||||||
| chrX:107913034
|
T | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2968T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913034 | ||||||
| chrX:107913038
|
A | AT | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1074-2963dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913038 | |||||
| chrX:107913039
|
T | TA | 2 | a0001c0001t0001g0106a0001c0002t0001g0172 | 2 | HG01891.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1074-2956dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913039 | |||||
| chrX:107913049
|
C | CAG | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1074-2951_1074-295 others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913049 | |||||
| chrX:107913064
|
A | G | 1 | a0001c0001t0004g0032 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1074-2938A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913064 | ||||||
| chrX:107913076
|
A | AC | 1 | a0001c0001t0006g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1074-2922dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913076 | |||||
| chrX:107913090
|
CT | C | 1 | a0002c0003t0002g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074-2908delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913090 | |||||
| chrX:107913115
|
TC | T | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1074-2885delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913115 | |||||
| chrX:107913156
|
A | AT | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2843dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913156 | |||||
| chrX:107913257
|
TA | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2741delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913257 | |||||
| chrX:107913368
|
C | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2634C>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913368 | ||||||
| chrX:107913408
|
TA | T | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1074-2592delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913408 | |||||
| chrX:107913411
|
TA | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2586delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913411 | |||||
| chrX:107913470
|
GA | G | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2529delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913470 | |||||
| chrX:107913549
|
G | T | 1 | a0001c0002t0002g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1074-2453G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913549 | ||||||
| chrX:107913553
|
TA | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2445delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913553 | |||||
| chrX:107913590
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124 | 3 | HG02622.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1074-2412C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913590 | ||||||
| chrX:107913631
|
A | AG | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2370dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913631 | |||||
| chrX:107913714
|
GT | G | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2284delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913714 | |||||
| chrX:107913753
|
TA | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2245delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913753 | |||||
| chrX:107913760
|
TG | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2240delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913760 | |||||
| chrX:107913849
|
T | TC | 1 | a0001c0001t0001g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1074-2149dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913849 | |||||
| chrX:107913850
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-2152C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913850 | ||||||
| chrX:107913869
|
A | AC | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1074-2128dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913869 | |||||
| chrX:107913883
|
TA | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2117delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913883 | |||||
| chrX:107913899
|
GT | G | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2100delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913899 | |||||
| chrX:107913926
|
C | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(4): Show | 7 | HG00642.hp1 HG02027.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074-2076C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107913926 | ||||||
| chrX:107913947
|
AG | A | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-2053delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107913947 | |||||
| chrX:107914019
|
G | A | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-1983G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914019 | ||||||
| chrX:107914150
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-1852T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914150 | ||||||
| chrX:107914182
|
G | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-1820G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914182 | ||||||
| chrX:107914205
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1074-1797T>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914205 | ||||||
| chrX:107914213
|
GC | G | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1074-1786delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107914213 | |||||
| chrX:107914286
|
T | C | 1 | a0001c0001t0012g0173 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1074-1716T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914286 | ||||||
| chrX:107914551
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-1451T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914551 | ||||||
| chrX:107914603
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-1399C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914603 | ||||||
| chrX:107914677
|
TG | T | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1074-1323delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107914677 | |||||
| chrX:107914824
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1074-1178A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107914824 | ||||||
| chrX:107915102
|
A | AT | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01192.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1074-894dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915102 | |||||
| chrX:107915113
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1074-889A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107915113 | ||||||
| chrX:107915197
|
TG | T | 1 | a0001c0001t0001g0030 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1074-802delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915197 | |||||
| chrX:107915428
|
GC | G | 10 | a0001c0001t0001g0165a0001c0001t0005g0016a0001c0001t0005g0017others(7): Show | 10 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074-572delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915428 | |||||
| chrX:107915461
|
G | GC | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1074-540dupC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915461 | |||||
| chrX:107915557
|
C | CA | 8 | a0001c0001t0001g0030a0001c0001t0001g0063a0001c0001t0001g0090others(5): Show | 8 | HG01192.hp1 HG02738.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1074-432dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915557 | |||||
| chrX:107915599
|
G | GT | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1074-401dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915599 | |||||
| chrX:107915673
|
C | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-329C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107915673 | ||||||
| chrX:107915710
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1074-292G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107915710 | ||||||
| chrX:107915750
|
CA | C | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1074-248delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915750 | |||||
| chrX:107915762
|
CG | C | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1074-238delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 107915762 | |||||
| chrX:107915776
|
T | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124 | 3 | HG02622.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1074-226T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 5/9 | chrX | 107915776 | ||||||
| chrX:107916162
|
A | AT | 1 | a0001c0001t0007g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1201+41dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107916162 | |||||
| chrX:107916196
|
T | C | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1201+67T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107916196 | ||||||
| chrX:107916294
|
GA | G | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1201+172delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107916294 | |||||
| chrX:107916347
|
AC | A | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1201+220delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107916347 | |||||
| chrX:107916457
|
A | G | 1 | a0001c0001t0010g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1201+328A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107916457 | ||||||
| chrX:107916604
|
TA | T | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1201+480delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107916604 | |||||
| chrX:107916674
|
GA | G | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1201+547delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107916674 | |||||
| chrX:107916856
|
T | TG | 1 | a0003c0007t0002g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1202-646dupG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107916856 | |||||
| chrX:107916869
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-637A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107916869 | ||||||
| chrX:107916986
|
CA | C | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1202-515delA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107916986 | |||||
| chrX:107917139
|
C | CTA | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202-354_1202-353d others(4): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107917139 | |||||
| chrX:107917139
|
C | CTATA | 4 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(1): Show | 4 | HG01106.hp1 HG01884.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202-356_1202-353d others(6): Show |
MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107917139 | |||||
| chrX:107917157
|
AT | A | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1202-345delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 107917157 | |||||
| chrX:107917352
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1202-154T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107917352 | ||||||
| chrX:107917423
|
G | C | 1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1202-83G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107917423 | ||||||
| chrX:107917428
|
C | T | 1 | a0001c0002t0002g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1202-78C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107917428 | ||||||
| chrX:107917429
|
G | A | 1 | a0002c0003t0002g0160 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1202-77G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 6/9 | chrX | 107917429 | ||||||
| chrX:107917799
|
TC | T | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1435+64delC | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 107917799 | |||||
| chrX:107918113
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1435+374C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107918113 | ||||||
| chrX:107918269
|
A | G | 26 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0046others(23): Show | 26 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1435+530A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107918269 | ||||||
| chrX:107918293
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1435+554T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107918293 | ||||||
| chrX:107918370
|
A | G | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435+631A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107918370 | ||||||
| chrX:107918574
|
TG | T | 1 | a0001c0001t0001g0044 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1435+839delG | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 107918574 | |||||
| chrX:107919254
|
G | T | 1 | a0001c0002t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1435+1515G>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107919254 | ||||||
| chrX:107919862
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1435+2123T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107919862 | ||||||
| chrX:107920537
|
A | G | 1 | a0001c0002t0002g0137 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1435+2798A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107920537 | ||||||
| chrX:107920708
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1435+2969A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107920708 | ||||||
| chrX:107920991
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1435+3252G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107920991 | ||||||
| chrX:107921624
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1436-2719C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107921624 | ||||||
| chrX:107921859
|
C | G | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436-2484C>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107921859 | ||||||
| chrX:107922074
|
A | G | 2 | a0001c0001t0008g0013a0001c0001t0008g0014 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1436-2269A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107922074 | ||||||
| chrX:107922259
|
A | G | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1436-2084A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107922259 | ||||||
| chrX:107922995
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1436-1348G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107922995 | ||||||
| chrX:107923052
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1436-1291A>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923052 | ||||||
| chrX:107923054
|
A | G | 5 | a0001c0001t0007g0139a0001c0001t0007g0166a0001c0001t0007g0167others(2): Show | 5 | HG01106.hp1 HG01884.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436-1289A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923054 | ||||||
| chrX:107923071
|
C | T | 1 | a0001c0002t0002g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1436-1272C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923071 | ||||||
| chrX:107923136
|
A | G | 1 | a0001c0002t0002g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1436-1207A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923136 | ||||||
| chrX:107923611
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1436-732A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923611 | ||||||
| chrX:107923760
|
T | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0134 | 3 | HG02630.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1436-583T>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | chrX | 107923760 | ||||||
| chrX:107924283
|
GT | G | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1436-55delT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chrX | 107924283 | |||||
| chrX:107924583
|
A | G | 9 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(6): Show | 9 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597+79A>G | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107924583 | ||||||
| chrX:107924611
|
G | C | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1597+107G>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107924611 | ||||||
| chrX:107924695
|
T | C | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | NA18960.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1597+191T>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107924695 | ||||||
| chrX:107924729
|
G | A | 11 | a0001c0001t0002g0178a0001c0001t0012g0173a0002c0003t0002g0138others(8): Show | 11 | HG00735.hp2 HG00741.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1597+225G>A | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107924729 | ||||||
| chrX:107925069
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597+565C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107925069 | ||||||
| chrX:107925229
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1597+725C>T | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107925229 | ||||||
| chrX:107925335
|
C | CA | 1 | a0001c0001t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1598-757dupA | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 107925335 | |||||
| chrX:107925870
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1598-224A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | chrX | 107925870 | ||||||
| chrX:107926066
|
C | CT | 1 | a0004c0004t0001g0110 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1598-16dupT | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 107926066 | |||||
| chrX:107926636
|
A | C | 5 | a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1806-35A>C | MID2 | ENSG00000080561.14 | transcript | ENST00000262843.11 | protein_coding | 9/9 | chrX | 107926636 |