Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4129 |
|---|---|
| ensemblid | ENSG00000069535.14 |
| hgncid | 6834 |
| symbol | MAOB |
| name | monoamine oxidase B |
| refseq_nuc | NM_000898.5 |
| refseq_prot | NP_000889.3 |
| ensembl_nuc | ENST00000378069.5 |
| ensembl_prot | ENSP00000367309.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 43766610 |
| end | 43882450 |
| strand | - |
| ver | v1.2 |
| region | chrX:43766610-43882450 |
| region5000 | chrX:43761610-43887450 |
| regionname0 | MAOB_chrX_43766610_43882450 |
| regionname5000 | MAOB_chrX_43761610_43887450 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 520 | 231 | 44 | 49 | 98 | 9 | 29 | 80 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0002 | 0/0 | 520 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0003 | 0/0 | 115 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0004 | 0/0 | 24 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1563 | 173 | 32 | 39 | 71 | 9 | 20 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| c0002 | 0/0 | 1563 | 42 | 0 | 6 | 27 | 0 | 9 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| c0003 | 0/0 | 1563 | 9 | 7 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| c0004 | 0/0 | 1563 | 4 | 4 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| c0005 | 0/0 | 1563 | 3 | 1 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| c0006 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| c0007 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| c0008 | 0/0 | 1564 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1008 | 164 | 23 | 41 | 68 | 9 | 21 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0002 | 0/0 | 1008 | 43 | 0 | 6 | 28 | 0 | 9 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0003 | 0/0 | 1008 | 10 | 10 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0004 | 0/0 | 1008 | 5 | 3 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0005 | 0/0 | 1008 | 3 | 3 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0006 | 0/0 | 1008 | 2 | 2 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0007 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0008 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0009 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0010 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0011 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0012 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| t0013 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1563 | 173 | 32 | 39 | 71 | 9 | 20 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0002 | 0/0 | 1563 | 42 | 0 | 6 | 27 | 0 | 9 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0003 | 0/0 | 1563 | 9 | 7 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0004 | 0/0 | 1563 | 4 | 4 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0005 | 0/0 | 1563 | 3 | 1 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0002c0007 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0003c0006 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0004c0008 | 0/0 | 1564 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2570 | 158 | 21 | 39 | 67 | 9 | 20 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0001t0003 | 0/0 | 2570 | 10 | 10 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0001t0008 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0001t0009 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0001t0011 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0001t0012 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0001t0013 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0002t0002 | 0/0 | 2570 | 42 | 0 | 6 | 27 | 0 | 9 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0003t0004 | 0/0 | 2570 | 5 | 3 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0003t0006 | 0/0 | 2570 | 2 | 2 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0003t0007 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0003t0010 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0004t0001 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0004t0005 | 0/0 | 2570 | 3 | 3 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0001c0005t0001 | 0/0 | 2570 | 3 | 1 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0002c0007t0001 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0003c0006t0002 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| a0004c0008t0001 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | copy fasta | chrX | 43761610 | 43887450 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0012g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0013g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0007g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0004t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0004t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0004t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0005t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0005t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0002c0007t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0003c0006t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0004c0008t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00642 | hp1 | a0001 | c0005 | t0001 | g0004 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | CHS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0189 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01081 | hp1 | a0001 | c0005 | t0001 | g0173 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01167 | hp1 | a0001 | c0003 | t0004 | g0187 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01169 | hp1 | a0001 | c0003 | t0004 | g0188 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0170 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01891 | hp1 | a0001 | c0003 | t0004 | g0186 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02056 | hp1 | a0002 | c0007 | t0001 | g0131 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0175 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | CDX | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02280 | hp2 | a0001 | c0003 | t0007 | g0001 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0232 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02723 | hp1 | a0001 | c0003 | t0010 | g0196 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02738 | hp1 | a0004 | c0008 | t0001 | g0234 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02809 | hp2 | a0001 | c0003 | t0006 | g0009 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02895 | hp1 | a0001 | c0004 | t0005 | g0013 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02897 | hp1 | a0001 | c0004 | t0005 | g0011 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02922 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0231 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0185 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0008 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03209 | hp1 | a0001 | c0004 | t0005 | g0012 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0214 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0010 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0220 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0218 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | CHB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | YRI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18945 | hp1 | a0001 | c0001 | t0013 | g0100 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18965 | hp1 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18985 | hp2 | a0003 | c0006 | t0002 | g0209 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0233 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0194 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19079 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0158 | REF | REF | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0177 | REF | REF | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| 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:43795854
|
C | G | 1 | a0002 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.653G>C | p.Ser218Thr | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/15 | 804/2570 | 653/1563 | 218/520 | chrX | 43795854 | ||
| chrX:43802209
|
T | TC | 1 | a0003 | 1 | NA18985.hp2 | frameshift_variant | HIGH | c.438dupG | p.Thr147fs | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/15 | 589/2570 | 438/1563 | 146/520 | chrX | 43802209 | ||
| chrX:43802232
|
A | AG | 1 | a0003 | 1 | NA18985.hp2 | frameshift_variant | HIGH | c.415dupC | p.Leu139fs | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/15 | 566/2570 | 415/1563 | 139/520 | chrX | 43802232 | ||
| chrX:43838868
|
C | CT | 1 | a0003 | 1 | NA18985.hp2 | frameshift_variant&splice_region_variant | HIGH | c.278dupA | p.Lys95fs | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/15 | 429/2570 | 278/1563 | 93/520 | chrX | 43838868 | ||
| chrX:43882264
|
G | GC | 1 | a0004 | 1 | HG02738.hp1 | frameshift_variant | HIGH | c.35dupG | p.Gly13fs | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/15 | 186/2570 | 35/1563 | 12/520 | chrX | 43882264 |
| 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:43767568
|
G | A | 2 | a0001c0002a0003c0006 | 43 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
synonymous_variant | LOW | c.1461C>T | p.Pro487Pro | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 1612/2570 | 1461/1563 | 487/520 | chrX | 43767568 | ||
| chrX:43780368
|
T | C | 1 | a0001c0003 | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
synonymous_variant | LOW | c.1053A>G | p.Lys351Lys | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/15 | 1204/2570 | 1053/1563 | 351/520 | chrX | 43780368 | ||
| chrX:43793510
|
T | C | 1 | a0001c0005 | 3 | HG00642.hp1 HG01081.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.837A>G | p.Pro279Pro | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/15 | 988/2570 | 837/1563 | 279/520 | chrX | 43793510 | ||
| chrX:43797137
|
T | C | 2 | a0001c0003a0001c0004 | 13 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(10): Show |
synonymous_variant | LOW | c.606A>G | p.Thr202Thr | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/15 | 757/2570 | 606/1563 | 202/520 | chrX | 43797137 |
| 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:43766622
|
A | G | 1 | a0001c0001t0012 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*844T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 844 | chrX | 43766622 | |||||
| chrX:43766665
|
A | G | 1 | a0001c0001t0011 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 801 | chrX | 43766665 | |||||
| chrX:43766669
|
T | G | 1 | a0001c0001t0013 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*797A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 797 | chrX | 43766669 | |||||
| chrX:43766708
|
T | C | 1 | a0001c0004t0005 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*758A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 758 | chrX | 43766708 | |||||
| chrX:43766838
|
A | G | 2 | a0001c0002t0002a0003c0006t0002 | 43 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*628T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 628 | chrX | 43766838 | |||||
| chrX:43766889
|
A | G | 7 | a0001c0002t0002a0001c0003t0004a0001c0003t0006others(4): Show | 55 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*577T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 577 | chrX | 43766889 | |||||
| chrX:43766892
|
G | T | 1 | a0001c0003t0010 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*574C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 574 | chrX | 43766892 | |||||
| chrX:43767082
|
A | T | 7 | a0001c0002t0002a0001c0003t0004a0001c0003t0006others(4): Show | 55 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*384T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 384 | chrX | 43767082 | |||||
| chrX:43767163
|
G | T | 2 | a0001c0003t0006a0001c0003t0007 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*303C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 303 | chrX | 43767163 | |||||
| chrX:43767234
|
A | G | 2 | a0001c0002t0002a0003c0006t0002 | 43 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*232T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 232 | chrX | 43767234 | |||||
| chrX:43767249
|
T | C | 1 | a0001c0001t0003 | 10 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*217A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 217 | chrX | 43767249 | |||||
| chrX:43767262
|
C | T | 4 | a0001c0001t0009a0001c0003t0006a0001c0003t0007others(1): Show | 7 | HG02280.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 15/15 | 204 | chrX | 43767262 | |||||
| chrX:43882412
|
C | T | 1 | a0001c0001t0008 | 1 | NA19090.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/15 | 113 | chrX | 43882412 | |||||
| chrX:43882423
|
C | T | 1 | a0001c0003t0007 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/15 | 124 | chrX | 43882423 |
| 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:43767621
|
A | G | 55 | a0001c0002t0002g0005a0001c0002t0002g0025a0001c0002t0002g0046others(52): Show | 55 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1411-3T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 14/14 | chrX | 43767621 | ||||||
| chrX:43767721
|
G | C | 50 | a0001c0002t0002g0005a0001c0002t0002g0025a0001c0002t0002g0046others(47): Show | 50 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1411-103C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 14/14 | chrX | 43767721 | ||||||
| chrX:43768145
|
G | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1410+509C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 14/14 | chrX | 43768145 | ||||||
| chrX:43768313
|
TC | T | 5 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1410+340delG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 14/14 | chrX | 43768313 | ||||||
| chrX:43768396
|
C | T | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1410+258G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 14/14 | chrX | 43768396 | ||||||
| chrX:43768418
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1410+236G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 14/14 | chrX | 43768418 | ||||||
| chrX:43768646
|
T | C | 5 | a0001c0001t0001g0180a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1410+8A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 14/14 | chrX | 43768646 | ||||||
| chrX:43768752
|
T | C | 89 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(86): Show | 89 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(86): Show |
intron_variant | MODIFIER | c.1348-36A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 13/14 | chrX | 43768752 | ||||||
| chrX:43768976
|
G | A | 1 | a0001c0003t0004g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1348-260C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 13/14 | chrX | 43768976 | ||||||
| chrX:43769300
|
A | G | 1 | a0001c0001t0003g0035 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.1347+7T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 13/14 | chrX | 43769300 | ||||||
| chrX:43769471
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1236-53T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43769471 | ||||||
| chrX:43769878
|
A | G | 1 | a0001c0002t0002g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1236-460T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43769878 | ||||||
| chrX:43769901
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1236-483T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43769901 | ||||||
| chrX:43769948
|
CACTTGCC others(3): Show |
C | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02572.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1236-540_1236-531d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43769948 | ||||||
| chrX:43770142
|
T | TA | 1 | a0001c0001t0001g0043 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1236-725dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770142 | ||||||
| chrX:43770192
|
G | T | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236-774C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770192 | ||||||
| chrX:43770213
|
C | T | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236-795G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770213 | ||||||
| chrX:43770306
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | NA18955.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1236-888C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770306 | ||||||
| chrX:43770335
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1236-917T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770335 | ||||||
| chrX:43770352
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1236-934G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770352 | ||||||
| chrX:43770465
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1236-1047T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770465 | ||||||
| chrX:43770485
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1236-1067G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770485 | ||||||
| chrX:43770693
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1236-1275G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770693 | ||||||
| chrX:43770698
|
A | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236-1280T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770698 | ||||||
| chrX:43770746
|
C | T | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1236-1328G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770746 | ||||||
| chrX:43770954
|
T | G | 50 | a0001c0002t0002g0005a0001c0002t0002g0025a0001c0002t0002g0046others(47): Show | 50 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1236-1536A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770954 | ||||||
| chrX:43770981
|
T | C | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1236-1563A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43770981 | ||||||
| chrX:43771215
|
A | C | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236-1797T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771215 | ||||||
| chrX:43771240
|
C | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1236-1822G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771240 | ||||||
| chrX:43771343
|
G | A | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1236-1925C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771343 | ||||||
| chrX:43771535
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1236-2117C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771535 | ||||||
| chrX:43771595
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1236-2177C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771595 | ||||||
| chrX:43771629
|
T | TTTACTTT others(724): Show |
1 | a0001c0001t0001g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1236-2212_1236-221 others(735): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771629 | ||||||
| chrX:43771629
|
T | TTTACTTT others(725): Show |
1 | a0001c0001t0001g0086 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1236-2212_1236-221 others(736): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771629 | ||||||
| chrX:43771633
|
C | CT | 51 | a0001c0001t0001g0057a0001c0002t0002g0005a0001c0002t0002g0025others(48): Show | 51 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1236-2216dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771633 | ||||||
| chrX:43771846
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1236-2428C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43771846 | ||||||
| chrX:43772255
|
A | T | 1 | a0001c0001t0011g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1236-2837T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43772255 | ||||||
| chrX:43772813
|
T | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0094a0001c0001t0001g0097others(2): Show | 5 | HG01943.hp1 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1235+2362A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43772813 | ||||||
| chrX:43772835
|
T | C | 50 | a0001c0002t0002g0005a0001c0002t0002g0025a0001c0002t0002g0046others(47): Show | 50 | HG00673.hp1 HG00735.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1235+2340A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43772835 | ||||||
| chrX:43772841
|
TC | T | 1 | a0001c0001t0001g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1235+2333delG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43772841 | ||||||
| chrX:43773025
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1235+2150G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43773025 | ||||||
| chrX:43773589
|
C | G | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1235+1586G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43773589 | ||||||
| chrX:43773697
|
G | T | 35 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(32): Show | 35 | HG00673.hp1 HG00735.hp1 HG02280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1235+1478C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43773697 | ||||||
| chrX:43773851
|
C | A | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235+1324G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43773851 | ||||||
| chrX:43773881
|
G | A | 40 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(37): Show | 40 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.1235+1294C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43773881 | ||||||
| chrX:43773881
|
G | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235+1294C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43773881 | ||||||
| chrX:43773915
|
T | C | 69 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0038others(66): Show | 69 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1235+1260A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43773915 | ||||||
| chrX:43774193
|
C | T | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235+982G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774193 | ||||||
| chrX:43774293
|
T | C | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235+882A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774293 | ||||||
| chrX:43774369
|
G | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1235+806C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774369 | ||||||
| chrX:43774493
|
G | A | 69 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0038others(66): Show | 69 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1235+682C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774493 | ||||||
| chrX:43774585
|
G | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG01175.hp1 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1235+590C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774585 | ||||||
| chrX:43774603
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1235+572A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774603 | ||||||
| chrX:43774723
|
T | C | 3 | a0001c0001t0003g0032a0001c0001t0003g0120a0001c0001t0003g0121 | 3 | HG02145.hp1 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1235+452A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774723 | ||||||
| chrX:43774756
|
T | C | 41 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(38): Show | 41 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.1235+419A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774756 | ||||||
| chrX:43774776
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1235+399G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774776 | ||||||
| chrX:43774834
|
A | G | 1 | a0001c0001t0003g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1235+341T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774834 | ||||||
| chrX:43774873
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1235+302A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43774873 | ||||||
| chrX:43775035
|
G | A | 8 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1235+140C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775035 | ||||||
| chrX:43775052
|
G | GT | 5 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0006g0008others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1235+122dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775052 | ||||||
| chrX:43775052
|
G | GTT | 2 | a0001c0003t0004g0187a0001c0003t0004g0188 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1235+121_1235+122d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775052 | ||||||
| chrX:43775052
|
G | GTTTT | 1 | a0001c0003t0004g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1235+122_1235+123i others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775052 | ||||||
| chrX:43775054
|
TG | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0050 | 3 | HG01074.hp1 HG01109.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1235+120delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775054 | ||||||
| chrX:43775055
|
G | GT | 10 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0078others(7): Show | 10 | HG00621.hp1 HG01081.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1235+119dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775055 | ||||||
| chrX:43775055
|
G | T | 8 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1235+120C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775055 | ||||||
| chrX:43775055
|
GT | G | 46 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0039others(43): Show | 46 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1235+119delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775055 | ||||||
| chrX:43775055
|
GTT | G | 2 | a0001c0002t0002g0215a0001c0004t0001g0233 | 2 | NA19030.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1235+118_1235+119d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775055 | ||||||
| chrX:43775055
|
GTTT | G | 4 | a0001c0003t0010g0196a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1235+117_1235+119d others(5): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775055 | ||||||
| chrX:43775145
|
C | T | 8 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1235+30G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 12/14 | chrX | 43775145 | ||||||
| chrX:43775281
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1138-9A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775281 | ||||||
| chrX:43775526
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02572.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1138-254G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775526 | ||||||
| chrX:43775554
|
T | A | 1 | a0001c0001t0001g0060 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1138-282A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775554 | ||||||
| chrX:43775654
|
A | T | 1 | a0001c0001t0001g0051 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1138-382T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775654 | ||||||
| chrX:43775716
|
AG | A | 1 | a0001c0002t0002g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1138-445delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775716 | ||||||
| chrX:43775813
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1138-541G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775813 | ||||||
| chrX:43775820
|
G | A | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1138-548C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775820 | ||||||
| chrX:43775917
|
C | T | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1138-645G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775917 | ||||||
| chrX:43776430
|
C | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG00099.hp1 HG01071.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138-1158G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776430 | ||||||
| chrX:43776441
|
A | G | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1138-1169T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776441 | ||||||
| chrX:43776554
|
C | CT | 2 | a0001c0001t0001g0019a0001c0001t0001g0180 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1138-1283dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776554 | ||||||
| chrX:43776554
|
CT | C | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1138-1283delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776554 | ||||||
| chrX:43776559
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1138-1287A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776559 | ||||||
| chrX:43776613
|
A | AT | 2 | a0001c0001t0001g0063a0001c0001t0001g0102 | 2 | HG00140.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1138-1342dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776613 | ||||||
| chrX:43776751
|
C | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0066 | 3 | HG03654.hp1 HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1138-1479G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776751 | ||||||
| chrX:43776754
|
T | TC | 1 | a0001c0003t0004g0188 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1138-1483dupG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776754 | ||||||
| chrX:43776754
|
T | TCC | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1138-1484_1138-148 others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776754 | ||||||
| chrX:43776761
|
T | TC | 1 | a0004c0008t0001g0234 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1138-1490dupG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776761 | ||||||
| chrX:43776899
|
C | T | 12 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1138-1627G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776899 | ||||||
| chrX:43776950
|
T | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1138-1678A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776950 | ||||||
| chrX:43777018
|
A | G | 1 | a0001c0002t0002g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1137+1664T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43777018 | ||||||
| chrX:43777059
|
G | A | 5 | a0001c0002t0002g0005a0001c0002t0002g0046a0001c0002t0002g0170others(2): Show | 5 | HG01081.hp2 HG01258.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137+1623C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43777059 | ||||||
| chrX:43777162
|
C | G | 1 | a0001c0002t0002g0231 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1137+1520G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43777162 | ||||||
| chrX:43777198
|
G | A | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137+1484C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43777198 | ||||||
| chrX:43777201
|
A | G | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1137+1481T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43777201 | ||||||
| chrX:43777550
|
G | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1137+1132C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43777550 | ||||||
| chrX:43777682
|
A | G | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1137+1000T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43777682 | ||||||
| chrX:43777973
|
C | T | 1 | a0001c0002t0002g0213 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1137+709G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43777973 | ||||||
| chrX:43778247
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0179 | 2 | HG02132.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1137+435T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43778247 | ||||||
| chrX:43778248
|
T | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0179 | 2 | HG02132.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1137+434A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43778248 | ||||||
| chrX:43778346
|
A | G | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1137+336T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43778346 | ||||||
| chrX:43778360
|
C | T | 1 | a0001c0002t0002g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1137+322G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43778360 | ||||||
| chrX:43778361
|
T | C | 1 | a0001c0002t0002g0025 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1137+321A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43778361 | ||||||
| chrX:43778412
|
T | C | 27 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0203others(24): Show | 27 | HG00673.hp1 HG02683.hp1 HG03017.hp1 others(24): Show |
intron_variant | MODIFIER | c.1137+270A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43778412 | ||||||
| chrX:43778521
|
G | C | 2 | a0001c0002t0002g0167a0001c0002t0002g0168 | 2 | NA18953.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1137+161C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43778521 | ||||||
| chrX:43778626
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1137+56G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43778626 | ||||||
| chrX:43778791
|
A | G | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1080-52T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43778791 | ||||||
| chrX:43778847
|
A | C | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1080-108T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43778847 | ||||||
| chrX:43778858
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0075 | 2 | HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1080-119C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43778858 | ||||||
| chrX:43779390
|
G | A | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080-651C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43779390 | ||||||
| chrX:43779428
|
TA | T | 1 | a0001c0001t0001g0128 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1080-690delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43779428 | ||||||
| chrX:43779533
|
A | G | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1080-794T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43779533 | ||||||
| chrX:43779690
|
G | C | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1079+652C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43779690 | ||||||
| chrX:43779705
|
G | A | 40 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(37): Show | 40 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.1079+637C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43779705 | ||||||
| chrX:43779788
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | NA19009.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1079+554C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43779788 | ||||||
| chrX:43779960
|
C | G | 8 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1079+382G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43779960 | ||||||
| chrX:43779983
|
C | T | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1079+359G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43779983 | ||||||
| chrX:43780046
|
G | A | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1079+296C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43780046 | ||||||
| chrX:43780107
|
G | T | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079+235C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43780107 | ||||||
| chrX:43780205
|
C | G | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1079+137G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43780205 | ||||||
| chrX:43780259
|
G | A | 1 | a0001c0002t0002g0189 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1079+83C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43780259 | ||||||
| chrX:43780292
|
TG | T | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1079+49delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43780292 | ||||||
| chrX:43780294
|
G | C | 2 | a0001c0002t0002g0224a0001c0002t0002g0230 | 2 | NA18959.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1079+48C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43780294 | ||||||
| chrX:43780299
|
GA | G | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1079+42delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 10/14 | chrX | 43780299 | ||||||
| chrX:43780581
|
C | T | 9 | a0001c0002t0002g0211a0001c0002t0002g0212a0001c0002t0002g0213others(6): Show | 9 | HG02683.hp1 HG03017.hp1 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-186G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43780581 | ||||||
| chrX:43780620
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1026-225T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43780620 | ||||||
| chrX:43780732
|
C | G | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.1026-337G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43780732 | ||||||
| chrX:43780866
|
A | T | 1 | a0001c0002t0002g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1026-471T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43780866 | ||||||
| chrX:43780904
|
C | A | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1026-509G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43780904 | ||||||
| chrX:43780991
|
C | T | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025+457G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43780991 | ||||||
| chrX:43781202
|
C | G | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025+246G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43781202 | ||||||
| chrX:43781345
|
T | TA | 17 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0042others(14): Show | 17 | HG01074.hp1 HG01109.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.1025+102dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43781345 | ||||||
| chrX:43781354
|
A | C | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1025+94T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43781354 | ||||||
| chrX:43781375
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1025+73C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 9/14 | chrX | 43781375 | ||||||
| chrX:43781557
|
C | A | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.929-13G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43781557 | ||||||
| chrX:43781557
|
C | T | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.929-13G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43781557 | ||||||
| chrX:43781699
|
A | G | 1 | a0001c0001t0003g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.929-155T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43781699 | ||||||
| chrX:43781707
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.929-163C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43781707 | ||||||
| chrX:43781889
|
A | G | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.929-345T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43781889 | ||||||
| chrX:43782104
|
C | T | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.929-560G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43782104 | ||||||
| chrX:43782128
|
TA | T | 4 | a0001c0002t0002g0215a0001c0002t0002g0223a0001c0002t0002g0224others(1): Show | 4 | NA18959.hp1 NA18998.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-585delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43782128 | ||||||
| chrX:43782178
|
CA | C | 1 | a0001c0002t0002g0168 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.929-635delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43782178 | ||||||
| chrX:43782279
|
T | C | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.929-735A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43782279 | ||||||
| chrX:43782401
|
T | C | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.929-857A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43782401 | ||||||
| chrX:43782735
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.929-1191T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43782735 | ||||||
| chrX:43782867
|
G | T | 1 | a0001c0001t0001g0034 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.929-1323C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43782867 | ||||||
| chrX:43783055
|
G | A | 9 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(6): Show | 9 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.929-1511C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43783055 | ||||||
| chrX:43783113
|
T | C | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.929-1569A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43783113 | ||||||
| chrX:43783821
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.929-2277G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43783821 | ||||||
| chrX:43783891
|
C | T | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.929-2347G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43783891 | ||||||
| chrX:43784563
|
G | A | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.929-3019C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43784563 | ||||||
| chrX:43784901
|
C | A | 40 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(37): Show | 40 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.929-3357G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43784901 | ||||||
| chrX:43784960
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.929-3416G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43784960 | ||||||
| chrX:43785043
|
G | T | 2 | a0001c0001t0003g0015a0001c0001t0003g0125 | 2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.929-3499C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785043 | ||||||
| chrX:43785113
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.929-3569C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785113 | ||||||
| chrX:43785119
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.929-3575C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785119 | ||||||
| chrX:43785193
|
T | C | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.929-3649A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785193 | ||||||
| chrX:43785436
|
T | G | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.929-3892A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785436 | ||||||
| chrX:43785444
|
A | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(1): Show | 4 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.929-3900T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785444 | ||||||
| chrX:43785482
|
T | C | 1 | a0001c0002t0002g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.929-3938A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785482 | ||||||
| chrX:43785632
|
C | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.929-4088G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785632 | ||||||
| chrX:43785994
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.929-4450G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785994 | ||||||
| chrX:43785996
|
C | T | 8 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.929-4452G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43785996 | ||||||
| chrX:43786200
|
C | T | 6 | a0001c0001t0001g0047a0001c0001t0001g0140a0001c0001t0001g0144others(3): Show | 6 | HG02523.hp1 NA18943.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.929-4656G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43786200 | ||||||
| chrX:43786255
|
G | C | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-4711C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43786255 | ||||||
| chrX:43786424
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.929-4880G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43786424 | ||||||
| chrX:43786749
|
G | T | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.929-5205C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43786749 | ||||||
| chrX:43786756
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.929-5212G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43786756 | ||||||
| chrX:43786765
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.929-5221G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43786765 | ||||||
| chrX:43786864
|
A | G | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.929-5320T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43786864 | ||||||
| chrX:43787104
|
A | T | 5 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0118others(2): Show | 5 | HG00609.hp1 NA18975.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-5560T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787104 | ||||||
| chrX:43787190
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0020 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.929-5646C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787190 | ||||||
| chrX:43787224
|
C | T | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.929-5680G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787224 | ||||||
| chrX:43787243
|
G | T | 12 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.929-5699C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787243 | ||||||
| chrX:43787358
|
AAATAAT | A | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.929-5820_929-5815d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787358 | ||||||
| chrX:43787399
|
CAT | C | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.929-5857_929-5856d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787399 | ||||||
| chrX:43787659
|
T | TATTTTTT others(24): Show |
5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+5759_928+5760i others(33): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787659 | ||||||
| chrX:43787867
|
G | T | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+5552C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787867 | ||||||
| chrX:43787912
|
C | T | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+5507G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43787912 | ||||||
| chrX:43788025
|
A | G | 12 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+5394T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43788025 | ||||||
| chrX:43788379
|
T | C | 1 | a0001c0001t0011g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.928+5040A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43788379 | ||||||
| chrX:43788394
|
A | T | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.928+5025T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43788394 | ||||||
| chrX:43788416
|
C | T | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.928+5003G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43788416 | ||||||
| chrX:43788663
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0126a0001c0001t0001g0159others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+4756C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43788663 | ||||||
| chrX:43788875
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.928+4544A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43788875 | ||||||
| chrX:43789221
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.928+4198C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43789221 | ||||||
| chrX:43789303
|
C | T | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+4116G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43789303 | ||||||
| chrX:43789379
|
T | C | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928+4040A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43789379 | ||||||
| chrX:43789444
|
T | C | 12 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0039others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+3975A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43789444 | ||||||
| chrX:43789602
|
G | A | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.928+3817C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43789602 | ||||||
| chrX:43789970
|
C | T | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(35): Show | 38 | HG00099.hp2 HG01074.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.928+3449G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43789970 | ||||||
| chrX:43790459
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0020 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.928+2960G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43790459 | ||||||
| chrX:43790500
|
T | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0094a0001c0001t0001g0097others(2): Show | 5 | HG01943.hp1 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+2919A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43790500 | ||||||
| chrX:43790585
|
C | CT | 3 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0002t0002g0219 | 3 | HG03139.hp1 NA18906.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.928+2833dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43790585 | ||||||
| chrX:43790625
|
G | A | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.928+2794C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43790625 | ||||||
| chrX:43790695
|
T | C | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.928+2724A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43790695 | ||||||
| chrX:43790726
|
T | G | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.928+2693A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43790726 | ||||||
| chrX:43790861
|
C | G | 1 | a0001c0001t0012g0028 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.928+2558G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43790861 | ||||||
| chrX:43791300
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.928+2119A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43791300 | ||||||
| chrX:43791344
|
C | A | 233 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.928+2075G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43791344 | ||||||
| chrX:43791581
|
C | T | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.928+1838G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43791581 | ||||||
| chrX:43791756
|
C | CA | 36 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(33): Show | 36 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.928+1662dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43791756 | ||||||
| chrX:43791948
|
A | G | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.928+1471T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43791948 | ||||||
| chrX:43791991
|
A | G | 1 | a0001c0003t0004g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.928+1428T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43791991 | ||||||
| chrX:43792002
|
G | A | 5 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+1417C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43792002 | ||||||
| chrX:43792052
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.928+1367A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43792052 | ||||||
| chrX:43792264
|
A | T | 232 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.928+1155T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43792264 | ||||||
| chrX:43792439
|
T | C | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0142 | 3 | NA18948.hp1 NA18971.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.928+980A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43792439 | ||||||
| chrX:43792611
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02572.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.928+808C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43792611 | ||||||
| chrX:43792806
|
G | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.928+613C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43792806 | ||||||
| chrX:43792880
|
C | T | 41 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(38): Show | 41 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.928+539G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43792880 | ||||||
| chrX:43793142
|
A | C | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+277T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43793142 | ||||||
| chrX:43793656
|
T | C | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.769-78A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43793656 | ||||||
| chrX:43793809
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.769-231T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43793809 | ||||||
| chrX:43794025
|
C | CA | 1 | a0001c0001t0001g0141 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.769-448dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794025 | ||||||
| chrX:43794157
|
T | G | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02572.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769-579A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794157 | ||||||
| chrX:43794271
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.769-693T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794271 | ||||||
| chrX:43794344
|
C | G | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.769-766G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794344 | ||||||
| chrX:43794467
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.769-889T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794467 | ||||||
| chrX:43794607
|
T | C | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.769-1029A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794607 | ||||||
| chrX:43794673
|
A | T | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+1066T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794673 | ||||||
| chrX:43794741
|
C | T | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.768+998G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794741 | ||||||
| chrX:43794832
|
C | G | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.768+907G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794832 | ||||||
| chrX:43794903
|
G | C | 8 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.768+836C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794903 | ||||||
| chrX:43794914
|
G | GA | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+824dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794914 | ||||||
| chrX:43794949
|
A | G | 1 | a0001c0002t0002g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.768+790T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794949 | ||||||
| chrX:43794988
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.768+751C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794988 | ||||||
| chrX:43794998
|
C | T | 1 | a0001c0002t0002g0231 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.768+741G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43794998 | ||||||
| chrX:43795352
|
A | G | 1 | a0001c0002t0002g0208 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.768+387T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43795352 | ||||||
| chrX:43795395
|
G | GCAGATAT others(2): Show |
28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.768+335_768+343dup others(9): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43795395 | ||||||
| chrX:43795505
|
A | T | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768+234T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43795505 | ||||||
| chrX:43795546
|
C | T | 1 | a0001c0002t0002g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.768+193G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43795546 | ||||||
| chrX:43795725
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.768+14T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43795725 | ||||||
| chrX:43795903
|
G | A | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-15C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43795903 | ||||||
| chrX:43796034
|
G | C | 9 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-146C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43796034 | ||||||
| chrX:43796328
|
TC | T | 1 | a0001c0002t0002g0167 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.619-441delG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43796328 | ||||||
| chrX:43796348
|
C | G | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.619-460G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43796348 | ||||||
| chrX:43796405
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.619-517G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43796405 | ||||||
| chrX:43796406
|
G | A | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-518C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43796406 | ||||||
| chrX:43796490
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.619-602G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43796490 | ||||||
| chrX:43796692
|
G | C | 1 | a0001c0002t0002g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.618+433C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43796692 | ||||||
| chrX:43796934
|
T | A | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.618+191A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 6/14 | chrX | 43796934 | ||||||
| chrX:43797313
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.477-47C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43797313 | ||||||
| chrX:43797595
|
C | A | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.477-329G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43797595 | ||||||
| chrX:43797631
|
C | A | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0070others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.477-365G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43797631 | ||||||
| chrX:43797827
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.477-561G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43797827 | ||||||
| chrX:43797924
|
C | G | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.477-658G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43797924 | ||||||
| chrX:43798012
|
C | T | 10 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.477-746G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798012 | ||||||
| chrX:43798245
|
T | C | 1 | a0001c0002t0002g0174 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.477-979A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798245 | ||||||
| chrX:43798288
|
A | G | 10 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.477-1022T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798288 | ||||||
| chrX:43798542
|
G | A | 36 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(33): Show | 36 | HG00099.hp2 HG01074.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.477-1276C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798542 | ||||||
| chrX:43798596
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.477-1330C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798596 | ||||||
| chrX:43798618
|
G | C | 38 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(35): Show | 38 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.477-1352C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798618 | ||||||
| chrX:43798766
|
G | A | 10 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.477-1500C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798766 | ||||||
| chrX:43798898
|
C | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.477-1632G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798898 | ||||||
| chrX:43798924
|
A | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.477-1658T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798924 | ||||||
| chrX:43798928
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.477-1662G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43798928 | ||||||
| chrX:43799128
|
T | C | 13 | a0001c0003t0004g0010a0001c0003t0004g0185a0001c0003t0004g0186others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.477-1862A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43799128 | ||||||
| chrX:43799226
|
G | C | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.477-1960C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43799226 | ||||||
| chrX:43799357
|
T | A | 2 | a0001c0005t0001g0004a0001c0005t0001g0173 | 2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.477-2091A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43799357 | ||||||
| chrX:43799457
|
G | T | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.477-2191C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43799457 | ||||||
| chrX:43799674
|
G | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.477-2408C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43799674 | ||||||
| chrX:43799687
|
G | A | 1 | a0001c0002t0002g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.477-2421C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43799687 | ||||||
| chrX:43800370
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.476+1802C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43800370 | ||||||
| chrX:43800370
|
G | T | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.476+1802C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43800370 | ||||||
| chrX:43800888
|
T | C | 71 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0038others(68): Show | 71 | HG00642.hp1 HG00673.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.476+1284A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43800888 | ||||||
| chrX:43800997
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.476+1175A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43800997 | ||||||
| chrX:43801054
|
AT | A | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.476+1117delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801054 | ||||||
| chrX:43801084
|
TC | T | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.476+1087delG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801084 | ||||||
| chrX:43801126
|
C | CT | 10 | a0001c0002t0002g0226a0001c0003t0004g0010a0001c0003t0004g0185others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.476+1045dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801126 | ||||||
| chrX:43801126
|
CT | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG01934.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.476+1045delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801126 | ||||||
| chrX:43801270
|
T | C | 2 | a0001c0002t0002g0213a0003c0006t0002g0209 | 2 | NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.476+902A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801270 | ||||||
| chrX:43801451
|
C | T | 8 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.476+721G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801451 | ||||||
| chrX:43801493
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.476+679T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801493 | ||||||
| chrX:43801827
|
GT | G | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.476+344delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801827 | ||||||
| chrX:43801903
|
C | T | 40 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(37): Show | 40 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.476+269G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801903 | ||||||
| chrX:43801920
|
A | AC | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.476+251dupG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801920 | ||||||
| chrX:43801922
|
C | T | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.476+250G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801922 | ||||||
| chrX:43801949
|
G | A | 3 | a0001c0002t0002g0216a0001c0002t0002g0217a0001c0002t0002g0227 | 3 | NA18977.hp1 NA18999.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.476+223C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801949 | ||||||
| chrX:43801971
|
C | CA | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.476+200dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801971 | ||||||
| chrX:43802030
|
C | T | 2 | a0001c0001t0003g0035a0001c0001t0003g0036 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.476+142G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43802030 | ||||||
| chrX:43802095
|
AT | A | 1 | a0001c0002t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.476+76delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43802095 | ||||||
| chrX:43802297
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0165 | 2 | NA18944.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.385-34T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802297 | ||||||
| chrX:43802397
|
TAA | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.385-136_385-135del others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802397 | ||||||
| chrX:43802453
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385-190A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802453 | ||||||
| chrX:43802461
|
C | T | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.385-198G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802461 | ||||||
| chrX:43802516
|
A | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 7 | HG01175.hp1 HG01978.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-253T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802516 | ||||||
| chrX:43802599
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.385-336A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802599 | ||||||
| chrX:43802677
|
A | G | 13 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.385-414T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802677 | ||||||
| chrX:43802756
|
A | T | 13 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.385-493T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802756 | ||||||
| chrX:43802784
|
T | TG | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.384+515dupC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802784 | ||||||
| chrX:43802825
|
T | C | 1 | a0001c0002t0002g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.384+475A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802825 | ||||||
| chrX:43802855
|
G | A | 1 | a0001c0002t0002g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.384+445C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43802855 | ||||||
| chrX:43803162
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.384+138A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 4/14 | chrX | 43803162 | ||||||
| chrX:43803637
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.280-233C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43803637 | ||||||
| chrX:43803652
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0145a0001c0001t0001g0148 | 3 | HG03831.hp2 NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.280-248G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43803652 | ||||||
| chrX:43804110
|
C | CA | 1 | a0001c0001t0001g0119 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280-707dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804110 | ||||||
| chrX:43804186
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.280-782C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804186 | ||||||
| chrX:43804313
|
C | T | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-909G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804313 | ||||||
| chrX:43804327
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.280-923A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804327 | ||||||
| chrX:43804450
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.280-1046C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804450 | ||||||
| chrX:43804454
|
AAAG | A | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.280-1053_280-1051d others(5): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804454 | ||||||
| chrX:43804455
|
A | AAGAGAG | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.280-1057_280-1052d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804455 | ||||||
| chrX:43804455
|
AAG | A | 9 | a0001c0002t0002g0211a0001c0002t0002g0212a0001c0002t0002g0213others(6): Show | 9 | HG02683.hp1 HG03017.hp1 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.280-1053_280-1052d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804455 | ||||||
| chrX:43804546
|
T | C | 1 | a0001c0003t0004g0188 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.280-1142A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804546 | ||||||
| chrX:43804547
|
G | A | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1143C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804547 | ||||||
| chrX:43804684
|
T | C | 1 | a0001c0002t0002g0232 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.280-1280A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804684 | ||||||
| chrX:43804910
|
G | A | 7 | a0001c0001t0001g0152a0001c0001t0003g0031a0001c0001t0003g0032others(4): Show | 7 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-1506C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804910 | ||||||
| chrX:43804958
|
G | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1554C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804958 | ||||||
| chrX:43805131
|
C | T | 1 | a0001c0002t0002g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.280-1727G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43805131 | ||||||
| chrX:43805238
|
T | G | 1 | a0001c0002t0002g0208 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.280-1834A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43805238 | ||||||
| chrX:43805278
|
T | TA | 45 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(42): Show | 45 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.280-1875dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43805278 | ||||||
| chrX:43805370
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.280-1966G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43805370 | ||||||
| chrX:43805512
|
T | C | 1 | a0001c0002t0002g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.280-2108A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43805512 | ||||||
| chrX:43806043
|
T | A | 1 | a0001c0001t0013g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.280-2639A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43806043 | ||||||
| chrX:43806085
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.280-2681T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43806085 | ||||||
| chrX:43806309
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0182 | 2 | HG01255.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.280-2905A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43806309 | ||||||
| chrX:43806582
|
T | C | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-3178A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43806582 | ||||||
| chrX:43806639
|
T | A | 1 | a0001c0002t0002g0174 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.280-3235A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43806639 | ||||||
| chrX:43806891
|
A | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-3487T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43806891 | ||||||
| chrX:43807376
|
G | C | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.280-3972C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43807376 | ||||||
| chrX:43807722
|
G | A | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-4318C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43807722 | ||||||
| chrX:43807869
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280-4465C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43807869 | ||||||
| chrX:43807882
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0089 | 2 | HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.280-4478G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43807882 | ||||||
| chrX:43807884
|
C | T | 5 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0118others(2): Show | 5 | HG00609.hp1 NA18975.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-4480G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43807884 | ||||||
| chrX:43808046
|
C | A | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-4642G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808046 | ||||||
| chrX:43808099
|
A | C | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-4695T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808099 | ||||||
| chrX:43808101
|
A | G | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.280-4697T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808101 | ||||||
| chrX:43808326
|
G | T | 1 | a0001c0002t0002g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.280-4922C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808326 | ||||||
| chrX:43808327
|
G | A | 1 | a0001c0002t0002g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.280-4923C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808327 | ||||||
| chrX:43808436
|
T | C | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-5032A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808436 | ||||||
| chrX:43808599
|
C | T | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.280-5195G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808599 | ||||||
| chrX:43808633
|
C | CATCTAT | 73 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(70): Show | 73 | HG00140.hp1 HG00621.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.280-5235_280-5230d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808633 | ||||||
| chrX:43808633
|
C | CATCTATA others(5): Show |
16 | a0001c0001t0001g0019a0001c0001t0001g0093a0001c0001t0001g0112others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.280-5241_280-5230d others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808633 | ||||||
| chrX:43808633
|
C | CATCTATA others(11): Show |
1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280-5247_280-5230d others(20): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808633 | ||||||
| chrX:43808633
|
C | CTTATCT | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-5230_280-5229i others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808633 | ||||||
| chrX:43808633
|
CATCTAT | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(46): Show | 49 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.280-5235_280-5230d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808633 | ||||||
| chrX:43808633
|
CATCTATA others(5): Show |
C | 3 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0117 | 3 | HG01978.hp2 NA18982.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.280-5241_280-5230d others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808633 | ||||||
| chrX:43808633
|
CATCTATA others(11): Show |
C | 6 | a0001c0001t0001g0041a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02165.hp1 HG02280.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-5247_280-5230d others(20): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808633 | ||||||
| chrX:43808681
|
T | C | 1 | a0001c0002t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.280-5277A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808681 | ||||||
| chrX:43808683
|
T | C | 1 | a0001c0002t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.280-5279A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808683 | ||||||
| chrX:43808684
|
C | A | 1 | a0001c0002t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.280-5280G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808684 | ||||||
| chrX:43808685
|
T | TAC | 1 | a0001c0002t0002g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.280-5282_280-5281i others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808685 | ||||||
| chrX:43808685
|
T | TACAC | 3 | a0001c0002t0002g0213a0001c0002t0002g0221a0003c0006t0002g0209 | 3 | HG04184.hp2 NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.280-5282_280-5281i others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808685 | ||||||
| chrX:43808687
|
T | C | 19 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0203others(16): Show | 19 | HG00673.hp1 HG02280.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.280-5283A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808687 | ||||||
| chrX:43808687
|
T | G | 1 | a0001c0002t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.280-5283A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808687 | ||||||
| chrX:43808689
|
T | C | 19 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0203others(16): Show | 19 | HG00673.hp1 HG02280.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.280-5285A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808689 | ||||||
| chrX:43808689
|
T | G | 3 | a0001c0002t0002g0213a0001c0002t0002g0221a0003c0006t0002g0209 | 3 | HG04184.hp2 NA18975.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.280-5285A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808689 | ||||||
| chrX:43808690
|
C | A | 23 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0203others(20): Show | 23 | HG00673.hp1 HG02280.hp2 HG02683.hp1 others(20): Show |
intron_variant | MODIFIER | c.280-5286G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808690 | ||||||
| chrX:43808691
|
T | C | 4 | a0001c0002t0002g0210a0001c0002t0002g0213a0001c0002t0002g0221others(1): Show | 4 | HG04184.hp2 NA18975.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-5287A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808691 | ||||||
| chrX:43808691
|
T | G | 1 | a0001c0002t0002g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.280-5287A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808691 | ||||||
| chrX:43808691
|
T | TAGACAC | 9 | a0001c0002t0002g0123a0001c0002t0002g0203a0001c0002t0002g0208others(6): Show | 9 | HG03239.hp1 HG04199.hp1 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.280-5288_280-5287i others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808691 | ||||||
| chrX:43808691
|
T | TAGACACA others(1): Show |
6 | a0001c0002t0002g0115a0001c0002t0002g0216a0001c0002t0002g0217others(3): Show | 6 | HG00673.hp1 NA18977.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-5288_280-5287i others(10): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808691 | ||||||
| chrX:43808691
|
T | TAGACACA others(3): Show |
1 | a0001c0002t0002g0232 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.280-5288_280-5287i others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808691 | ||||||
| chrX:43808691
|
T | TATATCTA others(17): Show |
1 | a0001c0002t0002g0231 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.280-5288_280-5287i others(26): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808691 | ||||||
| chrX:43808693
|
C | G | 2 | a0001c0003t0006g0009a0001c0003t0007g0001 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.280-5289G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808693 | ||||||
| chrX:43808695
|
CAT | C | 2 | a0001c0003t0006g0009a0001c0003t0007g0001 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.280-5293_280-5292d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808695 | ||||||
| chrX:43808697
|
T | C | 22 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0203others(19): Show | 22 | HG00673.hp1 HG02683.hp1 HG03017.hp1 others(19): Show |
intron_variant | MODIFIER | c.280-5293A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808697 | ||||||
| chrX:43808699
|
G | C | 24 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0203others(21): Show | 24 | HG00673.hp1 HG02280.hp2 HG02683.hp1 others(21): Show |
intron_variant | MODIFIER | c.280-5295C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808699 | ||||||
| chrX:43808699
|
G | GAC | 29 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0038others(26): Show | 29 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-5297_280-5296d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808699 | ||||||
| chrX:43808699
|
G | GACAC | 2 | a0001c0001t0001g0068a0001c0003t0006g0008 | 2 | HG01361.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.280-5299_280-5296d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808699 | ||||||
| chrX:43808699
|
G | GACACACA others(5): Show |
5 | a0001c0002t0002g0211a0001c0002t0002g0212a0001c0002t0002g0218others(2): Show | 5 | HG03669.hp2 HG03704.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-5307_280-5296d others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808699 | ||||||
| chrX:43808699
|
G | GACACACA others(11): Show |
1 | a0001c0002t0002g0189 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.280-5313_280-5296d others(20): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808699 | ||||||
| chrX:43808699
|
GAC | G | 2 | a0001c0003t0004g0010a0001c0004t0005g0012 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.280-5297_280-5296d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808699 | ||||||
| chrX:43808953
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-5549T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43808953 | ||||||
| chrX:43809132
|
T | C | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.280-5728A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43809132 | ||||||
| chrX:43809343
|
T | G | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-5939A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43809343 | ||||||
| chrX:43809413
|
G | A | 1 | a0001c0001t0013g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.280-6009C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43809413 | ||||||
| chrX:43809534
|
T | C | 1 | a0001c0002t0002g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.280-6130A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43809534 | ||||||
| chrX:43809572
|
T | C | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.280-6168A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43809572 | ||||||
| chrX:43809612
|
G | A | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-6208C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43809612 | ||||||
| chrX:43809667
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.280-6263G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43809667 | ||||||
| chrX:43809946
|
TGAAAGCT others(315): Show |
T | 17 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(14): Show | 17 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.280-6864_280-6543d others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43809946 | ||||||
| chrX:43810000
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0222 | 3 | NA18960.hp1 NA19003.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.280-6596A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810000 | ||||||
| chrX:43810199
|
C | T | 2 | a0001c0002t0002g0228a0001c0002t0002g0229 | 2 | NA19010.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.280-6795G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810199 | ||||||
| chrX:43810242
|
C | CA | 7 | a0001c0002t0002g0189a0001c0002t0002g0215a0001c0002t0002g0218others(4): Show | 7 | HG00735.hp1 HG04115.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-6839dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810242 | ||||||
| chrX:43810242
|
CA | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0018others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.280-6839delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810242 | ||||||
| chrX:43810242
|
CAA | C | 19 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0086others(16): Show | 19 | HG00099.hp2 HG01258.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.280-6840_280-6839d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810242 | ||||||
| chrX:43810269
|
G | A | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-6865C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810269 | ||||||
| chrX:43810468
|
T | A | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-7064A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810468 | ||||||
| chrX:43810603
|
T | TA | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-7200dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810603 | ||||||
| chrX:43810702
|
A | G | 41 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(38): Show | 41 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.280-7298T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810702 | ||||||
| chrX:43810702
|
A | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-7298T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810702 | ||||||
| chrX:43811511
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.280-8107A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43811511 | ||||||
| chrX:43811923
|
G | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.280-8519C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43811923 | ||||||
| chrX:43811926
|
G | A | 2 | a0001c0002t0002g0211a0001c0002t0002g0212 | 2 | NA18747.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.280-8522C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43811926 | ||||||
| chrX:43811989
|
A | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-8585T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43811989 | ||||||
| chrX:43812227
|
C | A | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-8823G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43812227 | ||||||
| chrX:43812485
|
T | C | 66 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0038others(63): Show | 66 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.280-9081A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43812485 | ||||||
| chrX:43812584
|
A | G | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.280-9180T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43812584 | ||||||
| chrX:43812684
|
A | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-9280T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43812684 | ||||||
| chrX:43812694
|
C | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-9290G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43812694 | ||||||
| chrX:43812893
|
A | G | 45 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(42): Show | 45 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.280-9489T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43812893 | ||||||
| chrX:43813084
|
T | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-9680A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43813084 | ||||||
| chrX:43813174
|
G | T | 1 | a0001c0001t0001g0014 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.280-9770C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43813174 | ||||||
| chrX:43813258
|
T | C | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-9854A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43813258 | ||||||
| chrX:43813280
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG00738.hp1 HG00741.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-9876G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43813280 | ||||||
| chrX:43813295
|
C | T | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-9891G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43813295 | ||||||
| chrX:43813314
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.280-9910C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43813314 | ||||||
| chrX:43813478
|
G | A | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-10074C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43813478 | ||||||
| chrX:43814108
|
T | A | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-10704A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43814108 | ||||||
| chrX:43814670
|
T | C | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.280-11266A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43814670 | ||||||
| chrX:43815367
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0182 | 2 | HG01255.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.280-11963G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43815367 | ||||||
| chrX:43815478
|
T | A | 1 | a0001c0001t0001g0057 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280-12074A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43815478 | ||||||
| chrX:43815665
|
C | A | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-12261G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43815665 | ||||||
| chrX:43815788
|
C | T | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0027others(35): Show | 38 | HG00099.hp2 HG01074.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.280-12384G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43815788 | ||||||
| chrX:43815842
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280-12438G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43815842 | ||||||
| chrX:43815881
|
CACAT | C | 1 | a0001c0001t0001g0029 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.280-12481_280-1247 others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43815881 | ||||||
| chrX:43816676
|
A | G | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-13272T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43816676 | ||||||
| chrX:43816810
|
G | T | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-13406C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43816810 | ||||||
| chrX:43816895
|
T | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.280-13491A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43816895 | ||||||
| chrX:43816934
|
A | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-13530T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43816934 | ||||||
| chrX:43817013
|
T | C | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.280-13609A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817013 | ||||||
| chrX:43817048
|
TCTC | T | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.280-13647_280-1364 others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817048 | ||||||
| chrX:43817079
|
CTCT | C | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.280-13678_280-1367 others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817079 | ||||||
| chrX:43817118
|
ATCT | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.280-13717_280-1371 others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817118 | ||||||
| chrX:43817269
|
C | T | 7 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-13865G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817269 | ||||||
| chrX:43817329
|
CT | C | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-13926delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817329 | ||||||
| chrX:43817368
|
C | A | 2 | a0001c0001t0003g0015a0001c0001t0003g0125 | 2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.280-13964G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817368 | ||||||
| chrX:43817546
|
G | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG01934.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.280-14142C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817546 | ||||||
| chrX:43817892
|
T | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0207 | 2 | HG00741.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.280-14488A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817892 | ||||||
| chrX:43817923
|
C | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.280-14519G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43817923 | ||||||
| chrX:43818151
|
A | C | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.280-14747T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43818151 | ||||||
| chrX:43818300
|
T | C | 7 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-14896A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43818300 | ||||||
| chrX:43818353
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0055 | 3 | HG00738.hp1 HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.280-14949G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43818353 | ||||||
| chrX:43818454
|
C | A | 3 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169 | 3 | NA18953.hp1 NA18957.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.280-15050G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43818454 | ||||||
| chrX:43818795
|
G | A | 67 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0038others(64): Show | 67 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.280-15391C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43818795 | ||||||
| chrX:43818858
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-15454G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43818858 | ||||||
| chrX:43818860
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.280-15456A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43818860 | ||||||
| chrX:43819356
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.280-15952T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43819356 | ||||||
| chrX:43819570
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-16166G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43819570 | ||||||
| chrX:43819760
|
G | A | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-16356C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43819760 | ||||||
| chrX:43819782
|
A | G | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.280-16378T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43819782 | ||||||
| chrX:43819793
|
T | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-16389A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43819793 | ||||||
| chrX:43820322
|
T | A | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-16918A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43820322 | ||||||
| chrX:43820350
|
A | T | 5 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(2): Show | 5 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-16946T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43820350 | ||||||
| chrX:43820384
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.280-16980T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43820384 | ||||||
| chrX:43820385
|
A | G | 46 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(43): Show | 46 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.280-16981T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43820385 | ||||||
| chrX:43820468
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.280-17064T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43820468 | ||||||
| chrX:43821467
|
G | A | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+17401C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43821467 | ||||||
| chrX:43821494
|
G | A | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+17374C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43821494 | ||||||
| chrX:43821523
|
A | G | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+17345T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43821523 | ||||||
| chrX:43821987
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.279+16881T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43821987 | ||||||
| chrX:43822846
|
T | TAACCAC | 1 | a0001c0002t0002g0189 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.279+16021_279+1602 others(10): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43822846 | ||||||
| chrX:43822846
|
T | TCAC | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+16019_279+1602 others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43822846 | ||||||
| chrX:43822872
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.279+15996T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43822872 | ||||||
| chrX:43822947
|
C | T | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+15921G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43822947 | ||||||
| chrX:43823165
|
C | CT | 25 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0052others(22): Show | 25 | HG00609.hp1 HG01934.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.279+15702dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823165 | ||||||
| chrX:43823165
|
C | CTT | 1 | a0001c0001t0001g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.279+15701_279+1570 others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823165 | ||||||
| chrX:43823165
|
CT | C | 38 | a0001c0001t0001g0077a0001c0001t0001g0140a0001c0001t0001g0161others(35): Show | 38 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.279+15702delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823165 | ||||||
| chrX:43823165
|
CTT | C | 3 | a0001c0001t0003g0031a0001c0001t0003g0035a0001c0002t0002g0115 | 3 | HG00673.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.279+15701_279+1570 others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823165 | ||||||
| chrX:43823165
|
CTTT | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+15700_279+1570 others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823165 | ||||||
| chrX:43823334
|
G | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279+15534C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823334 | ||||||
| chrX:43823465
|
G | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0003t0004g0010others(3): Show | 6 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+15403C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823465 | ||||||
| chrX:43823788
|
G | A | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+15080C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823788 | ||||||
| chrX:43823829
|
T | C | 1 | a0001c0002t0002g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.279+15039A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823829 | ||||||
| chrX:43823858
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.279+15010A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823858 | ||||||
| chrX:43823875
|
T | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.279+14993A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823875 | ||||||
| chrX:43823880
|
T | C | 28 | a0001c0002t0002g0115a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00673.hp1 HG00735.hp1 HG02683.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+14988A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43823880 | ||||||
| chrX:43824014
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.279+14854G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824014 | ||||||
| chrX:43824055
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+14813T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824055 | ||||||
| chrX:43824163
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+14705G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824163 | ||||||
| chrX:43824218
|
A | G | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+14650T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824218 | ||||||
| chrX:43824235
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.279+14633A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824235 | ||||||
| chrX:43824540
|
T | G | 46 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(43): Show | 46 | HG00673.hp1 HG00735.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.279+14328A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824540 | ||||||
| chrX:43824601
|
T | G | 1 | a0001c0001t0001g0051 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.279+14267A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824601 | ||||||
| chrX:43824682
|
C | CA | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.279+14185dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824682 | ||||||
| chrX:43824763
|
G | A | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+14105C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824763 | ||||||
| chrX:43824827
|
C | A | 27 | a0001c0002t0002g0123a0001c0002t0002g0189a0001c0002t0002g0203others(24): Show | 27 | HG00735.hp1 HG02683.hp1 HG03017.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+14041G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824827 | ||||||
| chrX:43824827
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0147 | 2 | NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.279+14041G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824827 | ||||||
| chrX:43824830
|
G | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0094a0001c0001t0001g0097others(2): Show | 5 | HG01943.hp1 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+14038C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824830 | ||||||
| chrX:43824969
|
A | C | 27 | a0001c0002t0002g0123a0001c0002t0002g0189a0001c0002t0002g0203others(24): Show | 27 | HG00735.hp1 HG02683.hp1 HG03017.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+13899T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824969 | ||||||
| chrX:43824998
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.279+13870A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824998 | ||||||
| chrX:43825383
|
A | AATTT | 1 | a0001c0001t0001g0157 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.279+13481_279+1348 others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43825383 | ||||||
| chrX:43825384
|
A | G | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+13484T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43825384 | ||||||
| chrX:43825516
|
C | G | 1 | a0001c0001t0001g0222 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.279+13352G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43825516 | ||||||
| chrX:43825751
|
A | G | 1 | a0001c0001t0008g0002 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.279+13117T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43825751 | ||||||
| chrX:43826105
|
G | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279+12763C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43826105 | ||||||
| chrX:43826751
|
C | A | 1 | a0001c0002t0002g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.279+12117G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43826751 | ||||||
| chrX:43826874
|
TG | T | 1 | a0001c0002t0002g0230 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.279+11993delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43826874 | ||||||
| chrX:43826951
|
T | C | 28 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00735.hp1 HG02683.hp1 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+11917A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43826951 | ||||||
| chrX:43827269
|
A | G | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+11599T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43827269 | ||||||
| chrX:43827516
|
C | T | 1 | a0001c0001t0003g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.279+11352G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43827516 | ||||||
| chrX:43828163
|
G | A | 1 | a0001c0002t0002g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.279+10705C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43828163 | ||||||
| chrX:43828378
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.279+10490A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43828378 | ||||||
| chrX:43828541
|
C | CA | 6 | a0001c0001t0001g0130a0001c0003t0004g0185a0001c0003t0004g0186others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+10326dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43828541 | ||||||
| chrX:43828786
|
C | A | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+10082G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43828786 | ||||||
| chrX:43829028
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.279+9840G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43829028 | ||||||
| chrX:43829718
|
A | C | 82 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(79): Show | 82 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.279+9150T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43829718 | ||||||
| chrX:43829789
|
C | A | 1 | a0001c0001t0001g0091 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.279+9079G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43829789 | ||||||
| chrX:43829990
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0049a0001c0001t0001g0075others(2): Show | 5 | HG00099.hp2 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+8878G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43829990 | ||||||
| chrX:43830036
|
A | G | 29 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0189others(26): Show | 29 | HG00735.hp1 HG02683.hp1 HG02723.hp1 others(26): Show |
intron_variant | MODIFIER | c.279+8832T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830036 | ||||||
| chrX:43830047
|
G | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.279+8821C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830047 | ||||||
| chrX:43830491
|
C | T | 1 | a0004c0008t0001g0234 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.279+8377G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830491 | ||||||
| chrX:43830505
|
T | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0147 | 2 | NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.279+8363A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830505 | ||||||
| chrX:43830580
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.279+8288T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830580 | ||||||
| chrX:43830736
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.279+8132G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830736 | ||||||
| chrX:43830994
|
A | AGTGTGT | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.279+7868_279+7873d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830994 | ||||||
| chrX:43830994
|
AGT | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0014others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.279+7872_279+7873d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830994 | ||||||
| chrX:43830994
|
AGTGT | A | 39 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0001g0129others(36): Show | 39 | HG00735.hp1 HG01243.hp1 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.279+7870_279+7873d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830994 | ||||||
| chrX:43830994
|
AGTGTGT | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0087others(7): Show | 10 | HG01175.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+7868_279+7873d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830994 | ||||||
| chrX:43830994
|
AGTGTGTG others(1): Show |
A | 8 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(5): Show | 8 | HG02280.hp1 HG02723.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+7866_279+7873d others(10): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830994 | ||||||
| chrX:43830994
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0004t0005g0011a0001c0004t0005g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.279+7864_279+7873d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830994 | ||||||
| chrX:43830994
|
AGTGTGTG others(7): Show |
A | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+7860_279+7873d others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43830994 | ||||||
| chrX:43831000
|
T | A | 2 | a0001c0001t0003g0035a0001c0001t0003g0036 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.279+7868A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43831000 | ||||||
| chrX:43831001
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.279+7867C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43831001 | ||||||
| chrX:43831068
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.279+7800T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43831068 | ||||||
| chrX:43831139
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.279+7729T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43831139 | ||||||
| chrX:43831363
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.279+7505C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43831363 | ||||||
| chrX:43831375
|
A | G | 28 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0189others(25): Show | 28 | HG00735.hp1 HG02683.hp1 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+7493T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43831375 | ||||||
| chrX:43831697
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0200 | 2 | HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.279+7171C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43831697 | ||||||
| chrX:43831944
|
C | A | 34 | a0001c0001t0001g0054a0001c0001t0001g0191a0001c0001t0001g0192others(31): Show | 34 | HG00735.hp1 HG02280.hp1 HG02683.hp1 others(31): Show |
intron_variant | MODIFIER | c.279+6924G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43831944 | ||||||
| chrX:43832051
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0026 | 2 | HG00280.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.279+6817G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43832051 | ||||||
| chrX:43832152
|
T | G | 5 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6716A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43832152 | ||||||
| chrX:43832252
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.279+6616A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43832252 | ||||||
| chrX:43832584
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02572.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.279+6284G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43832584 | ||||||
| chrX:43833049
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.279+5819T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43833049 | ||||||
| chrX:43833075
|
C | T | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG02280.hp1 HG02647.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+5793G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43833075 | ||||||
| chrX:43833211
|
A | C | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279+5657T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43833211 | ||||||
| chrX:43833308
|
G | A | 1 | a0001c0002t0002g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.279+5560C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43833308 | ||||||
| chrX:43833340
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0200 | 2 | HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.279+5528G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43833340 | ||||||
| chrX:43833397
|
T | C | 27 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0203others(24): Show | 27 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+5471A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43833397 | ||||||
| chrX:43833700
|
AAACT | A | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+5164_279+5167d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43833700 | ||||||
| chrX:43833717
|
CA | C | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.279+5150delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43833717 | ||||||
| chrX:43834825
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.279+4043C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43834825 | ||||||
| chrX:43834838
|
G | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.279+4030C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43834838 | ||||||
| chrX:43835873
|
A | C | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+2995T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43835873 | ||||||
| chrX:43836372
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.279+2496T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43836372 | ||||||
| chrX:43836397
|
T | C | 3 | a0001c0002t0002g0005a0001c0005t0001g0004a0001c0005t0001g0006 | 3 | HG00642.hp1 HG01081.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.279+2471A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43836397 | ||||||
| chrX:43836542
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.279+2326C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43836542 | ||||||
| chrX:43836957
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.279+1911T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43836957 | ||||||
| chrX:43837131
|
C | T | 1 | a0001c0004t0005g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.279+1737G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43837131 | ||||||
| chrX:43837339
|
G | C | 2 | a0001c0002t0002g0210a0003c0006t0002g0209 | 2 | NA18983.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.279+1529C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43837339 | ||||||
| chrX:43837572
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.279+1296G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43837572 | ||||||
| chrX:43837701
|
G | A | 2 | a0001c0002t0002g0210a0003c0006t0002g0209 | 2 | NA18983.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.279+1167C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43837701 | ||||||
| chrX:43837828
|
G | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0145a0001c0001t0001g0148 | 3 | HG03831.hp2 NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.279+1040C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43837828 | ||||||
| chrX:43838033
|
G | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.279+835C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838033 | ||||||
| chrX:43838075
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.279+793C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838075 | ||||||
| chrX:43838122
|
C | T | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+746G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838122 | ||||||
| chrX:43838251
|
GC | G | 5 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+616delG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838251 | ||||||
| chrX:43838294
|
T | C | 28 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0203others(25): Show | 28 | HG02683.hp1 HG02723.hp1 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+574A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838294 | ||||||
| chrX:43838351
|
G | GA | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.279+516_279+517ins others(1): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838351 | ||||||
| chrX:43838392
|
C | T | 28 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0203others(25): Show | 28 | HG02683.hp1 HG02723.hp1 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+476G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838392 | ||||||
| chrX:43838607
|
G | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.279+261C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838607 | ||||||
| chrX:43838675
|
T | TA | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG01934.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.279+192dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838675 | ||||||
| chrX:43838854
|
TG | T | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.279+13delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43838854 | ||||||
| chrX:43839013
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19083.hp1 | splice_region_variant&intron_variant | LOW | c.142-8G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839013 | ||||||
| chrX:43839050
|
T | TA | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.142-46dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839050 | ||||||
| chrX:43839380
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142-375T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839380 | ||||||
| chrX:43839430
|
A | AG | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.142-426dupC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839430 | ||||||
| chrX:43839449
|
T | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-444A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839449 | ||||||
| chrX:43839629
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.142-624A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839629 | ||||||
| chrX:43839914
|
GC | G | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.142-910delG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839914 | ||||||
| chrX:43840053
|
C | A | 2 | a0001c0001t0001g0054a0001c0002t0002g0123 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.142-1048G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840053 | ||||||
| chrX:43840084
|
A | G | 1 | a0001c0003t0004g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-1079T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840084 | ||||||
| chrX:43840171
|
C | CA | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.142-1167_142-1166i others(3): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840171 | ||||||
| chrX:43840303
|
T | A | 1 | a0001c0001t0001g0042 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142-1298A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840303 | ||||||
| chrX:43840462
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.142-1457C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840462 | ||||||
| chrX:43840655
|
T | TG | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.142-1651dupC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840655 | ||||||
| chrX:43840702
|
TC | T | 1 | a0003c0006t0002g0209 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.142-1698delG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840702 | ||||||
| chrX:43840747
|
T | C | 12 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0169others(9): Show | 12 | HG01081.hp1 HG01258.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-1742A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840747 | ||||||
| chrX:43840878
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02572.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.142-1873C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840878 | ||||||
| chrX:43840893
|
G | GT | 15 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0079others(12): Show | 15 | HG02027.hp1 HG02056.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-1889dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840893 | ||||||
| chrX:43840893
|
GT | G | 42 | a0001c0001t0001g0054a0001c0001t0001g0069a0001c0001t0001g0072others(39): Show | 42 | HG00735.hp1 HG01934.hp1 HG02132.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-1889delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840893 | ||||||
| chrX:43840893
|
GTT | G | 6 | a0001c0002t0002g0211a0001c0003t0004g0185a0001c0003t0004g0186others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-1890_142-1889d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840893 | ||||||
| chrX:43840951
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.142-1946G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840951 | ||||||
| chrX:43841058
|
A | G | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.142-2053T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841058 | ||||||
| chrX:43841059
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.142-2054T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841059 | ||||||
| chrX:43841348
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2322G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841348 | ||||||
| chrX:43841527
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.141+2143T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841527 | ||||||
| chrX:43841553
|
A | T | 18 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0203others(15): Show | 18 | HG03239.hp1 HG03669.hp2 HG03927.hp2 others(15): Show |
intron_variant | MODIFIER | c.141+2117T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841553 | ||||||
| chrX:43841728
|
A | C | 28 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0203others(25): Show | 28 | HG02683.hp1 HG02723.hp1 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.141+1942T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841728 | ||||||
| chrX:43841781
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+1889A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841781 | ||||||
| chrX:43841789
|
C | A | 2 | a0001c0002t0002g0210a0003c0006t0002g0209 | 2 | NA18983.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.141+1881G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841789 | ||||||
| chrX:43841937
|
G | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.141+1733C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43841937 | ||||||
| chrX:43842358
|
A | T | 2 | a0001c0001t0003g0015a0001c0001t0003g0125 | 2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.141+1312T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43842358 | ||||||
| chrX:43842485
|
C | G | 2 | a0001c0002t0002g0210a0003c0006t0002g0209 | 2 | NA18983.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.141+1185G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43842485 | ||||||
| chrX:43842501
|
G | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0086 | 2 | NA19009.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.141+1169C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43842501 | ||||||
| chrX:43842620
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.141+1050G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43842620 | ||||||
| chrX:43843355
|
TCTCACAC others(5): Show |
T | 14 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0170others(11): Show | 14 | HG01081.hp1 HG01258.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.141+303_141+314del others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843355 | ||||||
| chrX:43843355
|
TCTCACAC others(9): Show |
T | 1 | a0001c0002t0002g0169 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.141+299_141+314del others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843355 | ||||||
| chrX:43843357
|
T | TCA | 6 | a0001c0001t0001g0018a0001c0001t0001g0093a0001c0001t0001g0145others(3): Show | 6 | HG02071.hp1 HG04228.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+311_141+312dup others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
T | TCACA | 1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.141+309_141+312dup others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCA | T | 37 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0022others(34): Show | 37 | HG00609.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.141+311_141+312del others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCACA | T | 37 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.141+309_141+312del others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCACACA | T | 17 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0061others(14): Show | 17 | HG01952.hp1 HG02040.hp1 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.141+307_141+312del others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCACACAC others(1): Show |
T | 11 | a0001c0001t0001g0021a0001c0001t0001g0049a0001c0001t0001g0110others(8): Show | 11 | HG00099.hp2 HG01169.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.141+305_141+312del others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCACACAC others(3): Show |
T | 10 | a0001c0001t0001g0056a0001c0001t0001g0124a0001c0003t0004g0010others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+303_141+312del others(10): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.141+301_141+312del others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCACACAC others(7): Show |
T | 23 | a0001c0001t0001g0054a0001c0002t0002g0123a0001c0002t0002g0203others(20): Show | 23 | HG03017.hp1 HG03239.hp1 HG03669.hp2 others(20): Show |
intron_variant | MODIFIER | c.141+299_141+312del others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCACACAC others(9): Show |
T | 4 | a0001c0002t0002g0210a0001c0002t0002g0230a0001c0002t0002g0232others(1): Show | 4 | HG02683.hp1 NA18959.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+297_141+312del others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843357
|
TCACACAC others(11): Show |
T | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+295_141+312del others(18): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843357 | ||||||
| chrX:43843361
|
A | T | 4 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+309T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843361 | ||||||
| chrX:43843363
|
A | T | 1 | a0001c0001t0003g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.141+307T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843363 | ||||||
| chrX:43843377
|
A | T | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+293T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843377 | ||||||
| chrX:43843436
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+234G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43843436 | ||||||
| chrX:43844544
|
T | C | 34 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0037others(31): Show | 34 | HG00099.hp2 HG01074.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.47-780A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43844544 | ||||||
| chrX:43845035
|
A | G | 42 | a0001c0001t0001g0054a0001c0001t0001g0190a0001c0001t0001g0191others(39): Show | 42 | HG00735.hp1 HG02280.hp1 HG02280.hp2 others(39): Show |
intron_variant | MODIFIER | c.47-1271T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43845035 | ||||||
| chrX:43845138
|
A | AT | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-1375dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43845138 | ||||||
| chrX:43845595
|
G | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-1831C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43845595 | ||||||
| chrX:43845597
|
C | T | 34 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0037others(31): Show | 34 | HG00099.hp2 HG01074.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.47-1833G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43845597 | ||||||
| chrX:43845605
|
AAC | A | 1 | a0001c0001t0003g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47-1843_47-1842del others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43845605 | ||||||
| chrX:43845615
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.47-1851A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43845615 | ||||||
| chrX:43845777
|
T | C | 1 | a0001c0002t0002g0213 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.47-2013A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43845777 | ||||||
| chrX:43845823
|
C | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-2059G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43845823 | ||||||
| chrX:43846180
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.47-2416A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43846180 | ||||||
| chrX:43846204
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.47-2440G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43846204 | ||||||
| chrX:43846305
|
G | A | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.47-2541C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43846305 | ||||||
| chrX:43846328
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.47-2564A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43846328 | ||||||
| chrX:43846560
|
GA | G | 1 | a0001c0002t0002g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.47-2797delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43846560 | ||||||
| chrX:43846973
|
G | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0050others(2): Show | 5 | HG01074.hp1 HG01109.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-3209C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43846973 | ||||||
| chrX:43847003
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-3239T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847003 | ||||||
| chrX:43847034
|
C | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-3270G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847034 | ||||||
| chrX:43847061
|
T | C | 30 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(27): Show | 30 | HG02280.hp2 HG02683.hp1 HG02723.hp1 others(27): Show |
intron_variant | MODIFIER | c.47-3297A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847061 | ||||||
| chrX:43847156
|
C | T | 41 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(38): Show | 41 | HG00735.hp1 HG02280.hp1 HG02280.hp2 others(38): Show |
intron_variant | MODIFIER | c.47-3392G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847156 | ||||||
| chrX:43847173
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0164 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.47-3409C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847173 | ||||||
| chrX:43847221
|
G | A | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-3457C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847221 | ||||||
| chrX:43847238
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.47-3474C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847238 | ||||||
| chrX:43847398
|
T | G | 46 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(43): Show | 46 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.47-3634A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847398 | ||||||
| chrX:43847412
|
G | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-3648C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847412 | ||||||
| chrX:43847613
|
A | T | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-3849T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43847613 | ||||||
| chrX:43848031
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.47-4267C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43848031 | ||||||
| chrX:43848055
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.47-4291A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43848055 | ||||||
| chrX:43848103
|
G | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0094a0001c0001t0001g0097others(2): Show | 5 | HG01943.hp1 HG01978.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-4339C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43848103 | ||||||
| chrX:43848135
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.47-4371C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43848135 | ||||||
| chrX:43848507
|
G | GT | 30 | a0001c0001t0001g0027a0001c0001t0001g0222a0001c0002t0002g0203others(27): Show | 30 | HG01175.hp1 HG02280.hp2 HG02683.hp1 others(27): Show |
intron_variant | MODIFIER | c.47-4744dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43848507 | ||||||
| chrX:43849271
|
A | G | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-5507T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43849271 | ||||||
| chrX:43849322
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.47-5558T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43849322 | ||||||
| chrX:43849514
|
T | A | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.47-5750A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43849514 | ||||||
| chrX:43849528
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.47-5764C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43849528 | ||||||
| chrX:43849893
|
T | C | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-6129A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43849893 | ||||||
| chrX:43850031
|
C | T | 5 | a0001c0001t0001g0093a0001c0001t0001g0110a0001c0001t0001g0179others(2): Show | 5 | HG02132.hp1 NA18965.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-6267G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43850031 | ||||||
| chrX:43850472
|
C | T | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.47-6708G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43850472 | ||||||
| chrX:43850486
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.47-6722C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43850486 | ||||||
| chrX:43850542
|
G | A | 46 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(43): Show | 46 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.47-6778C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43850542 | ||||||
| chrX:43850617
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.47-6853T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43850617 | ||||||
| chrX:43850644
|
GA | G | 2 | a0001c0001t0001g0205a0001c0001t0008g0002 | 2 | NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.47-6881delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43850644 | ||||||
| chrX:43851162
|
G | A | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-7398C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43851162 | ||||||
| chrX:43851461
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.47-7697G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43851461 | ||||||
| chrX:43851490
|
A | G | 30 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(27): Show | 30 | HG02280.hp2 HG02683.hp1 HG02723.hp1 others(27): Show |
intron_variant | MODIFIER | c.47-7726T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43851490 | ||||||
| chrX:43851522
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.47-7758T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43851522 | ||||||
| chrX:43852112
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47-8348C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852112 | ||||||
| chrX:43852247
|
C | T | 1 | a0001c0002t0002g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.47-8483G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852247 | ||||||
| chrX:43852356
|
C | G | 1 | a0001c0002t0002g0115 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.47-8592G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852356 | ||||||
| chrX:43852690
|
T | G | 1 | a0001c0001t0001g0222 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.47-8926A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852690 | ||||||
| chrX:43852813
|
A | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0166 | 3 | HG02074.hp1 NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.47-9049T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852813 | ||||||
| chrX:43852908
|
G | T | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.47-9144C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852908 | ||||||
| chrX:43852951
|
AG | A | 1 | a0001c0001t0001g0043 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.47-9188delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852951 | ||||||
| chrX:43852961
|
CTGGGGAG others(1): Show |
C | 1 | a0001c0001t0008g0002 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.47-9205_47-9198del others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852961 | ||||||
| chrX:43853129
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.47-9365C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853129 | ||||||
| chrX:43853267
|
C | CA | 37 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0079others(34): Show | 37 | HG00735.hp1 HG02280.hp1 HG02280.hp2 others(34): Show |
intron_variant | MODIFIER | c.47-9504dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853267 | ||||||
| chrX:43853267
|
C | CAA | 1 | a0001c0001t0011g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.47-9505_47-9504dup others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853267 | ||||||
| chrX:43853267
|
C | CAAA | 1 | a0001c0002t0002g0220 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.47-9506_47-9504dup others(3): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853267 | ||||||
| chrX:43853267
|
CA | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0065a0001c0001t0001g0094others(4): Show | 7 | HG01243.hp1 HG01943.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-9504delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853267 | ||||||
| chrX:43853267
|
CAAAA | C | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.47-9507_47-9504del others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853267 | ||||||
| chrX:43853278
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.47-9526_47-9515del others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853278 | ||||||
| chrX:43853285
|
A | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 13 | HG01256.hp1 HG01261.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.47-9521T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853285 | ||||||
| chrX:43853632
|
T | TG | 1 | a0001c0002t0002g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.47-9869dupC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853632 | ||||||
| chrX:43853744
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-9980G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853744 | ||||||
| chrX:43853747
|
T | C | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.47-9983A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853747 | ||||||
| chrX:43853816
|
C | T | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-10052G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43853816 | ||||||
| chrX:43854230
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.47-10466A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43854230 | ||||||
| chrX:43854274
|
C | T | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-10510G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43854274 | ||||||
| chrX:43854508
|
G | GT | 1 | a0001c0003t0004g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.47-10745dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43854508 | ||||||
| chrX:43854828
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.47-11064G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43854828 | ||||||
| chrX:43854836
|
C | T | 41 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(38): Show | 41 | HG00735.hp1 HG02280.hp1 HG02280.hp2 others(38): Show |
intron_variant | MODIFIER | c.47-11072G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43854836 | ||||||
| chrX:43854893
|
G | A | 46 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(43): Show | 46 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.47-11129C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43854893 | ||||||
| chrX:43854962
|
G | C | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-11198C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43854962 | ||||||
| chrX:43855005
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.47-11241T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855005 | ||||||
| chrX:43855048
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47-11284G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855048 | ||||||
| chrX:43855151
|
T | C | 1 | a0001c0002t0002g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.47-11387A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855151 | ||||||
| chrX:43855334
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.47-11570G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855334 | ||||||
| chrX:43855363
|
G | C | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-11599C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855363 | ||||||
| chrX:43855399
|
C | CGT | 27 | a0001c0001t0001g0222a0001c0002t0002g0174a0001c0002t0002g0203others(24): Show | 27 | HG02056.hp1 HG02683.hp1 HG03017.hp1 others(24): Show |
intron_variant | MODIFIER | c.47-11637_47-11636d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855399 | ||||||
| chrX:43855399
|
C | CGTGT | 1 | a0001c0002t0002g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.47-11639_47-11636d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855399 | ||||||
| chrX:43855399
|
CGT | C | 1 | a0001c0002t0002g0115 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.47-11637_47-11636d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855399 | ||||||
| chrX:43855495
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.47-11731A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855495 | ||||||
| chrX:43855511
|
G | C | 46 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(43): Show | 46 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.47-11747C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855511 | ||||||
| chrX:43855521
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-11757G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855521 | ||||||
| chrX:43855630
|
A | G | 5 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0118others(2): Show | 5 | HG00609.hp1 NA18975.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-11866T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855630 | ||||||
| chrX:43855922
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0091a0001c0001t0001g0117others(1): Show | 4 | HG02071.hp1 NA18940.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-12158C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855922 | ||||||
| chrX:43855938
|
G | A | 46 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(43): Show | 46 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.47-12174C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855938 | ||||||
| chrX:43855992
|
A | G | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-12228T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43855992 | ||||||
| chrX:43856036
|
T | TAAAACA | 1 | a0001c0001t0008g0002 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.47-12278_47-12273d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856036 | ||||||
| chrX:43856049
|
A | C | 1 | a0001c0002t0002g0220 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.47-12285T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856049 | ||||||
| chrX:43856088
|
T | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-12324A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856088 | ||||||
| chrX:43856095
|
TTC | T | 1 | a0001c0001t0001g0092 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.47-12333_47-12332d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856095 | ||||||
| chrX:43856616
|
T | C | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-12852A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856616 | ||||||
| chrX:43856864
|
G | A | 5 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-13100C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856864 | ||||||
| chrX:43856880
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.47-13116T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856880 | ||||||
| chrX:43856955
|
A | AT | 5 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-13192dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856955 | ||||||
| chrX:43856955
|
AT | A | 35 | a0001c0001t0001g0086a0001c0001t0001g0135a0001c0001t0001g0147others(32): Show | 35 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(32): Show |
intron_variant | MODIFIER | c.47-13192delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43856955 | ||||||
| chrX:43857079
|
CT | C | 1 | a0001c0001t0008g0002 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.47-13316delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857079 | ||||||
| chrX:43857081
|
TTA | T | 1 | a0001c0001t0001g0056 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.47-13319_47-13318d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857081 | ||||||
| chrX:43857082
|
TA | T | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.47-13319delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857082 | ||||||
| chrX:43857084
|
A | AAT | 10 | a0001c0001t0001g0016a0001c0001t0001g0076a0001c0001t0001g0094others(7): Show | 10 | HG01943.hp1 HG02293.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.47-13322_47-13321d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | AATAT | 8 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0099others(5): Show | 8 | HG01258.hp1 HG01981.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.47-13324_47-13321d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | AATATAT | 3 | a0001c0001t0001g0097a0001c0001t0001g0150a0001c0001t0001g0205 | 3 | HG01978.hp2 NA18994.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.47-13326_47-13321d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | AATATATA others(1): Show |
7 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0144others(4): Show | 7 | HG01517.hp1 HG01993.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-13328_47-13321d others(10): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | AATATATA others(3): Show |
4 | a0001c0001t0001g0140a0001c0002t0002g0221a0001c0002t0002g0226others(1): Show | 4 | HG02683.hp1 HG03927.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-13330_47-13321d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | AATATATA others(5): Show |
2 | a0001c0002t0002g0211a0001c0002t0002g0231 | 2 | HG03017.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.47-13332_47-13321d others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.47-13338_47-13321d others(20): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | AATATATA others(15): Show |
1 | a0001c0002t0002g0212 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.47-13342_47-13321d others(24): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | AT | 2 | a0001c0001t0001g0137a0001c0002t0002g0136 | 2 | HG02523.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.47-13321_47-13320i others(3): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
A | T | 1 | a0001c0001t0008g0002 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.47-13320T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
AAT | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0204a0001c0003t0004g0186 | 3 | HG00741.hp1 HG01891.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.47-13322_47-13321d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
AATATATA others(3): Show |
A | 2 | a0001c0001t0001g0017a0001c0001t0001g0065 | 2 | HG01891.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.47-13330_47-13321d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857084
|
AATATATA others(9): Show |
A | 1 | a0001c0002t0002g0203 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.47-13336_47-13321d others(18): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857084 | ||||||
| chrX:43857104
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0001g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.47-13362_47-13341d others(24): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857104 | ||||||
| chrX:43857104
|
TATATATA others(21): Show |
T | 1 | a0001c0001t0003g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.47-13368_47-13341d others(30): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857104 | ||||||
| chrX:43857108
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0003g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.47-13354_47-13345d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857108 | ||||||
| chrX:43857108
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0180a0001c0001t0003g0121 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.47-13358_47-13345d others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857108 | ||||||
| chrX:43857108
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0001g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.47-13362_47-13345d others(20): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857108 | ||||||
| chrX:43857108
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.47-13364_47-13345d others(22): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857108 | ||||||
| chrX:43857108
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0001g0040 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.47-13368_47-13345d others(26): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857108 | ||||||
| chrX:43857110
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0152a0001c0001t0003g0033 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.47-13356_47-13347d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857110 | ||||||
| chrX:43857110
|
TATATATA others(13): Show |
T | 2 | a0001c0001t0001g0159a0001c0001t0001g0164 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.47-13366_47-13347d others(22): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857110 | ||||||
| chrX:43857110
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0001g0023a0001c0001t0001g0073 | 2 | HG00741.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.47-13368_47-13347d others(24): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857110 | ||||||
| chrX:43857110
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.47-13370_47-13347d others(26): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857110 | ||||||
| chrX:43857110
|
TATATATA others(19): Show |
T | 2 | a0001c0001t0001g0022a0001c0001t0001g0200 | 2 | HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.47-13372_47-13347d others(28): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857110 | ||||||
| chrX:43857110
|
TATATATA others(25): Show |
T | 1 | a0001c0001t0001g0154 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.47-13378_47-13347d others(34): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857110 | ||||||
| chrX:43857112
|
T | G | 3 | a0001c0004t0005g0011a0001c0004t0005g0012a0001c0004t0005g0013 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.47-13348A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857112 | ||||||
| chrX:43857112
|
TATATAGA others(3): Show |
T | 2 | a0001c0001t0001g0061a0001c0001t0003g0120 | 2 | HG02258.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.47-13358_47-13349d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857112 | ||||||
| chrX:43857112
|
TATATAGA others(5): Show |
T | 2 | a0001c0001t0001g0060a0001c0001t0003g0125 | 2 | NA18906.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.47-13360_47-13349d others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857112 | ||||||
| chrX:43857112
|
TATATAGA others(7): Show |
T | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.47-13362_47-13349d others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857112 | ||||||
| chrX:43857112
|
TATATAGA others(13): Show |
T | 5 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0126others(2): Show | 5 | HG00099.hp1 HG01099.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-13368_47-13349d others(22): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857112 | ||||||
| chrX:43857112
|
TATATAGA others(15): Show |
T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01934.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.47-13370_47-13349d others(24): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857112 | ||||||
| chrX:43857112
|
TATATAGA others(17): Show |
T | 1 | a0001c0001t0001g0039 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.47-13372_47-13349d others(26): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857112 | ||||||
| chrX:43857112
|
TATATAGA others(19): Show |
T | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.47-13374_47-13349d others(28): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857112 | ||||||
| chrX:43857114
|
T | G | 6 | a0001c0002t0002g0208a0001c0002t0002g0210a0001c0004t0005g0011others(3): Show | 6 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-13350A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857114 | ||||||
| chrX:43857114
|
TATAG | T | 1 | a0001c0001t0001g0003 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.47-13354_47-13351d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857114 | ||||||
| chrX:43857114
|
TATAGAG | T | 1 | a0001c0001t0001g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47-13356_47-13351d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857114 | ||||||
| chrX:43857114
|
TATAGAGA others(3): Show |
T | 1 | a0001c0001t0003g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.47-13360_47-13351d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857114 | ||||||
| chrX:43857114
|
TATAGAGA others(7): Show |
T | 1 | a0001c0001t0001g0049 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.47-13364_47-13351d others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857114 | ||||||
| chrX:43857114
|
TATAGAGA others(13): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.47-13370_47-13351d others(22): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857114 | ||||||
| chrX:43857114
|
TATAGAGA others(15): Show |
T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG01358.hp1 HG01361.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.47-13372_47-13351d others(24): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857114 | ||||||
| chrX:43857114
|
TATAGAGA others(17): Show |
T | 1 | a0001c0001t0001g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.47-13374_47-13351d others(26): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857114 | ||||||
| chrX:43857116
|
T | G | 13 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0002t0002g0123others(10): Show | 13 | HG02622.hp1 HG02735.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.47-13352A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
T | TAG | 2 | a0001c0001t0001g0018a0001c0001t0001g0066 | 2 | HG03831.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.47-13354_47-13353d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
T | TATATAGA others(1): Show |
1 | a0001c0001t0001g0145 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.47-13353_47-13352i others(10): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
T | TATATATA others(5): Show |
1 | a0001c0003t0006g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.47-13353_47-13352i others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
T | TATATATA others(7): Show |
1 | a0001c0003t0006g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.47-13353_47-13352i others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0202 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.47-13353_47-13352i others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
T | TATATATA others(17): Show |
1 | a0001c0003t0007g0001 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.47-13353_47-13352i others(26): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
TAG | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0001t0001g0085others(14): Show | 17 | HG00609.hp1 HG01081.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-13354_47-13353d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
TAGAG | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0058others(21): Show | 24 | HG01978.hp1 HG01993.hp1 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.47-13356_47-13353d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
TAGAGAG | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0001g0086others(6): Show | 9 | HG00140.hp1 HG01074.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.47-13358_47-13353d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
TAGAGAGA others(1): Show |
T | 6 | a0001c0001t0001g0051a0001c0001t0001g0134a0001c0001t0001g0151others(3): Show | 6 | HG00673.hp1 HG02965.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-13360_47-13353d others(10): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
TAGAGAGA others(3): Show |
T | 9 | a0001c0001t0001g0021a0001c0001t0001g0052a0001c0001t0001g0053others(6): Show | 9 | HG01169.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.47-13362_47-13353d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
TAGAGAGA others(5): Show |
T | 9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(6): Show | 9 | HG02004.hp1 HG02004.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.47-13364_47-13353d others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
TAGAGAGA others(7): Show |
T | 3 | a0001c0001t0001g0147a0001c0001t0001g0157a0001c0001t0003g0036 | 3 | HG03225.hp1 HG04228.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.47-13366_47-13353d others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857116
|
TAGAGAGA others(11): Show |
T | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.47-13370_47-13353d others(20): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857116 | ||||||
| chrX:43857118
|
G | T | 76 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(73): Show | 76 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.47-13354C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857118 | ||||||
| chrX:43857120
|
G | T | 77 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0026others(74): Show | 77 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.47-13356C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857120 | ||||||
| chrX:43857122
|
G | T | 79 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0024others(76): Show | 79 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.47-13358C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857122 | ||||||
| chrX:43857124
|
G | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0024others(64): Show | 67 | HG00280.hp1 HG00609.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.47-13360C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857124 | ||||||
| chrX:43857126
|
G | T | 48 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0029others(45): Show | 48 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.47-13362C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857126 | ||||||
| chrX:43857128
|
G | T | 36 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0024others(33): Show | 36 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.47-13364C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857128 | ||||||
| chrX:43857130
|
G | T | 28 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0042others(25): Show | 28 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.47-13366C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857130 | ||||||
| chrX:43857132
|
G | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0083others(7): Show | 10 | HG02083.hp1 HG03831.hp2 HG04228.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-13368C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857132 | ||||||
| chrX:43857134
|
G | GATATATA others(39): Show |
1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.47-13371_47-13370i others(48): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857134 | ||||||
| chrX:43857134
|
G | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0147a0001c0001t0001g0157others(1): Show | 4 | HG04228.hp1 NA18953.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-13370C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857134 | ||||||
| chrX:43857136
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0197 | 2 | HG02809.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.47-13372C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857136 | ||||||
| chrX:43857138
|
G | T | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.47-13374C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857138 | ||||||
| chrX:43857147
|
AGAGAGAG others(8): Show |
A | 3 | a0001c0002t0002g0005a0001c0003t0010g0196a0001c0005t0001g0006 | 3 | HG01081.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.47-13398_47-13384d others(17): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857147 | ||||||
| chrX:43857149
|
AGAGAGAG others(6): Show |
A | 1 | a0001c0005t0001g0004 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.47-13398_47-13386d others(15): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857149 | ||||||
| chrX:43857151
|
AGAGAGAG others(4): Show |
A | 4 | a0001c0001t0001g0020a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG02622.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-13398_47-13388d others(13): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857151 | ||||||
| chrX:43857153
|
AGAGAGAG others(2): Show |
A | 4 | a0001c0001t0001g0034a0001c0001t0001g0122a0001c0001t0001g0190others(1): Show | 4 | HG02280.hp1 HG02647.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-13398_47-13390d others(11): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857153 | ||||||
| chrX:43857155
|
AG | A | 3 | a0001c0002t0002g0203a0001c0002t0002g0210a0001c0002t0002g0212 | 3 | NA18747.hp1 NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.47-13392delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857155 | ||||||
| chrX:43857155
|
AGAGAGAG | A | 1 | a0001c0002t0002g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.47-13398_47-13392d others(9): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857155 | ||||||
| chrX:43857156
|
G | GA | 2 | a0001c0001t0001g0222a0003c0006t0002g0209 | 2 | NA18985.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.47-13393dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857156 | ||||||
| chrX:43857157
|
AG | A | 2 | a0001c0004t0005g0011a0001c0004t0005g0012 | 2 | HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.47-13394delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857157 | ||||||
| chrX:43857157
|
AGAGAG | A | 3 | a0001c0001t0011g0194a0001c0003t0004g0187a0001c0003t0004g0188 | 3 | HG01167.hp1 HG01169.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.47-13398_47-13394d others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857157 | ||||||
| chrX:43857159
|
AGAG | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG00621.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.47-13398_47-13396d others(5): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857159 | ||||||
| chrX:43857160
|
G | A | 14 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0210others(11): Show | 14 | HG02683.hp1 HG02895.hp1 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.47-13396C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857160 | ||||||
| chrX:43857160
|
GAGAGA | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0080others(2): Show | 5 | HG01109.hp1 HG02015.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-13401_47-13397d others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857160 | ||||||
| chrX:43857161
|
A | AAGAAG | 4 | a0001c0002t0002g0208a0001c0002t0002g0215a0001c0002t0002g0224others(1): Show | 4 | NA18957.hp2 NA18959.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-13398_47-13397i others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857161 | ||||||
| chrX:43857161
|
A | G | 14 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0210others(11): Show | 14 | HG02683.hp1 HG02895.hp1 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.47-13397T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857161 | ||||||
| chrX:43857161
|
AG | A | 5 | a0001c0001t0001g0180a0001c0002t0002g0189a0001c0003t0004g0185others(2): Show | 5 | HG00735.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-13398delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857161 | ||||||
| chrX:43857162
|
G | A | 18 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(15): Show | 18 | HG02683.hp1 HG02895.hp1 HG03017.hp1 others(15): Show |
intron_variant | MODIFIER | c.47-13398C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857162 | ||||||
| chrX:43857162
|
G | GAAGAAGA | 1 | a0001c0002t0002g0227 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.47-13399_47-13398i others(9): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857162 | ||||||
| chrX:43857162
|
G | GAGAGAAG others(4): Show |
1 | a0001c0002t0002g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.47-13399_47-13398i others(13): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857162 | ||||||
| chrX:43857162
|
G | GAGAGAGA others(12): Show |
1 | a0001c0002t0002g0213 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.47-13399_47-13398i others(21): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857162 | ||||||
| chrX:43857165
|
A | AG | 3 | a0001c0001t0001g0179a0001c0003t0006g0008a0001c0003t0006g0009 | 3 | HG02132.hp1 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-13402_47-13401i others(3): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857165 | ||||||
| chrX:43857167
|
GA | G | 17 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0122others(14): Show | 17 | HG00621.hp1 HG00735.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-13404delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857167 | ||||||
| chrX:43857168
|
A | AAG | 1 | a0001c0001t0003g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.47-13406_47-13405d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857168 | ||||||
| chrX:43857168
|
A | AAGAAGAA others(3): Show |
6 | a0001c0002t0002g0214a0001c0002t0002g0216a0001c0002t0002g0217others(3): Show | 6 | HG03239.hp1 HG04115.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-13405_47-13404i others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857168 | ||||||
| chrX:43857168
|
A | AAGAAGAA others(5): Show |
1 | a0001c0002t0002g0220 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.47-13405_47-13404i others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857168 | ||||||
| chrX:43857168
|
A | AAGAG | 3 | a0001c0002t0002g0221a0001c0002t0002g0223a0001c0002t0002g0231 | 3 | HG03017.hp1 HG04184.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.47-13408_47-13405d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857168 | ||||||
| chrX:43857168
|
A | AAGAGAG | 2 | a0001c0002t0002g0211a0001c0002t0002g0219 | 2 | NA19054.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.47-13410_47-13405d others(8): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857168 | ||||||
| chrX:43857168
|
A | AG | 18 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0192others(15): Show | 18 | HG00642.hp1 HG01081.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.47-13405_47-13404i others(3): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857168 | ||||||
| chrX:43857168
|
A | AGAG | 3 | a0001c0002t0002g0212a0001c0002t0002g0230a0003c0006t0002g0209 | 3 | NA18747.hp1 NA18959.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.47-13405_47-13404i others(5): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857168 | ||||||
| chrX:43857168
|
AAG | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0067a0001c0001t0001g0068others(11): Show | 14 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.47-13406_47-13405d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857168 | ||||||
| chrX:43857170
|
G | GA | 2 | a0001c0003t0006g0008a0001c0003t0006g0009 | 2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-13407dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857170 | ||||||
| chrX:43857171
|
AG | A | 1 | a0001c0001t0001g0030 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.47-13408delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857171 | ||||||
| chrX:43857171
|
AGAG | A | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.47-13410_47-13408d others(5): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857171 | ||||||
| chrX:43857368
|
T | C | 27 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(24): Show | 27 | HG02683.hp1 HG02723.hp1 HG03017.hp1 others(24): Show |
intron_variant | MODIFIER | c.47-13604A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857368 | ||||||
| chrX:43857424
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.47-13660G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857424 | ||||||
| chrX:43857642
|
C | T | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-13878G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857642 | ||||||
| chrX:43857845
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0180 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.47-14081A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857845 | ||||||
| chrX:43858234
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.47-14470G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43858234 | ||||||
| chrX:43858367
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-14603G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43858367 | ||||||
| chrX:43858544
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-14780G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43858544 | ||||||
| chrX:43858570
|
C | T | 1 | a0001c0002t0002g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.47-14806G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43858570 | ||||||
| chrX:43858608
|
G | A | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-14844C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43858608 | ||||||
| chrX:43858732
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.47-14968G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43858732 | ||||||
| chrX:43859041
|
C | T | 3 | a0001c0002t0002g0005a0001c0005t0001g0004a0001c0005t0001g0006 | 3 | HG00642.hp1 HG01081.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.47-15277G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43859041 | ||||||
| chrX:43859484
|
G | A | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-15720C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43859484 | ||||||
| chrX:43859731
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.47-15967A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43859731 | ||||||
| chrX:43859749
|
C | T | 1 | a0001c0002t0002g0214 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.47-15985G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43859749 | ||||||
| chrX:43860004
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-16240G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43860004 | ||||||
| chrX:43860021
|
T | C | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-16257A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43860021 | ||||||
| chrX:43860054
|
C | G | 9 | a0001c0001t0001g0034a0001c0001t0001g0152a0001c0001t0003g0031others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.47-16290G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43860054 | ||||||
| chrX:43860870
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.47-17106C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43860870 | ||||||
| chrX:43860907
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.47-17143G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43860907 | ||||||
| chrX:43861045
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.47-17281C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861045 | ||||||
| chrX:43861243
|
C | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-17479G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861243 | ||||||
| chrX:43861519
|
G | A | 8 | a0001c0003t0004g0010a0001c0003t0006g0008a0001c0003t0006g0009others(5): Show | 8 | HG02280.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-17755C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861519 | ||||||
| chrX:43861557
|
T | C | 8 | a0001c0003t0004g0010a0001c0003t0006g0008a0001c0003t0006g0009others(5): Show | 8 | HG02280.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-17793A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861557 | ||||||
| chrX:43861856
|
C | CGT | 10 | a0001c0001t0001g0017a0001c0001t0001g0077a0001c0001t0001g0116others(7): Show | 10 | HG00673.hp1 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-18094_47-18093d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861856 | ||||||
| chrX:43861856
|
C | CGTGT | 3 | a0001c0003t0004g0185a0001c0003t0004g0187a0001c0003t0004g0188 | 3 | HG01167.hp1 HG01169.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.47-18096_47-18093d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861856 | ||||||
| chrX:43861856
|
C | CGTGTGTG others(3): Show |
2 | a0001c0003t0006g0008a0001c0003t0006g0009 | 2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-18102_47-18093d others(12): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861856 | ||||||
| chrX:43861856
|
C | CGTGTGTG others(5): Show |
1 | a0001c0003t0007g0001 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.47-18104_47-18093d others(14): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861856 | ||||||
| chrX:43861856
|
CGT | C | 40 | a0001c0001t0001g0074a0001c0001t0001g0126a0001c0001t0001g0159others(37): Show | 40 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.47-18094_47-18093d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861856 | ||||||
| chrX:43861856
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0135a0001c0001t0001g0147 | 2 | NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.47-18106_47-18093d others(16): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861856 | ||||||
| chrX:43861872
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0180 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.47-18108A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861872 | ||||||
| chrX:43861920
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47-18156G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861920 | ||||||
| chrX:43861969
|
A | G | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-18205T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43861969 | ||||||
| chrX:43862112
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.47-18348T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43862112 | ||||||
| chrX:43862215
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.47-18451A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43862215 | ||||||
| chrX:43862464
|
G | T | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.47-18700C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43862464 | ||||||
| chrX:43862643
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0147a0001c0001t0001g0149 | 3 | NA18960.hp1 NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.47-18879G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43862643 | ||||||
| chrX:43862766
|
A | G | 8 | a0001c0002t0002g0211a0001c0002t0002g0212a0001c0002t0002g0213others(5): Show | 8 | HG02683.hp1 HG03017.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.47-19002T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43862766 | ||||||
| chrX:43862855
|
C | CA | 2 | a0001c0002t0002g0228a0001c0002t0002g0229 | 2 | NA19010.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.47-19092dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43862855 | ||||||
| chrX:43862871
|
A | G | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-19107T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43862871 | ||||||
| chrX:43862908
|
A | G | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.47-19144T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43862908 | ||||||
| chrX:43863322
|
G | T | 1 | a0001c0001t0012g0028 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.46+18932C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43863322 | ||||||
| chrX:43863368
|
T | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+18886A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43863368 | ||||||
| chrX:43863372
|
A | G | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+18882T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43863372 | ||||||
| chrX:43864676
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46+17578C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43864676 | ||||||
| chrX:43864786
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.46+17468G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43864786 | ||||||
| chrX:43864945
|
G | GAC | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+17307_46+17308d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43864945 | ||||||
| chrX:43865032
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.46+17222T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43865032 | ||||||
| chrX:43865042
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.46+17212G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43865042 | ||||||
| chrX:43865047
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.46+17207C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43865047 | ||||||
| chrX:43865057
|
C | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG00735.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+17197G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43865057 | ||||||
| chrX:43865058
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46+17196C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43865058 | ||||||
| chrX:43865785
|
C | CT | 1 | a0001c0001t0001g0127 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.46+16468dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43865785 | ||||||
| chrX:43865785
|
CT | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0112a0001c0001t0001g0113others(5): Show | 8 | HG02683.hp2 HG02738.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.46+16468delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43865785 | ||||||
| chrX:43866589
|
C | T | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+15665G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43866589 | ||||||
| chrX:43866812
|
C | T | 6 | a0001c0001t0001g0152a0001c0001t0003g0031a0001c0001t0003g0032others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+15442G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43866812 | ||||||
| chrX:43866965
|
A | G | 1 | a0001c0003t0006g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46+15289T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43866965 | ||||||
| chrX:43867133
|
C | T | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+15121G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43867133 | ||||||
| chrX:43867144
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.46+15110A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43867144 | ||||||
| chrX:43867148
|
A | G | 127 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(124): Show | 127 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(124): Show |
intron_variant | MODIFIER | c.46+15106T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43867148 | ||||||
| chrX:43867616
|
C | A | 1 | a0001c0003t0004g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46+14638G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43867616 | ||||||
| chrX:43868358
|
T | TC | 1 | a0001c0001t0001g0014 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.46+13895dupG | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868358 | ||||||
| chrX:43868362
|
C | T | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+13892G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868362 | ||||||
| chrX:43868456
|
A | G | 3 | a0001c0002t0002g0216a0001c0002t0002g0217a0001c0002t0002g0227 | 3 | NA18977.hp1 NA18999.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.46+13798T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868456 | ||||||
| chrX:43868661
|
T | C | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.46+13593A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868661 | ||||||
| chrX:43868803
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.46+13451C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868803 | ||||||
| chrX:43868848
|
T | A | 1 | a0001c0002t0002g0115 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.46+13406A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868848 | ||||||
| chrX:43868855
|
T | TTG | 16 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(13): Show | 16 | HG00735.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.46+13397_46+13398d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868855 | ||||||
| chrX:43868855
|
T | TTGTG | 5 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0003t0004g0187others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+13395_46+13398d others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868855 | ||||||
| chrX:43868855
|
TTG | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0119a0001c0001t0001g0160 | 3 | HG02015.hp1 NA18967.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.46+13397_46+13398d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868855 | ||||||
| chrX:43868969
|
C | T | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+13285G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43868969 | ||||||
| chrX:43869027
|
T | G | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.46+13227A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43869027 | ||||||
| chrX:43869342
|
C | G | 45 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 45 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.46+12912G>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43869342 | ||||||
| chrX:43869686
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0012g0028 | 2 | NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.46+12568T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43869686 | ||||||
| chrX:43869805
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.46+12449C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43869805 | ||||||
| chrX:43869904
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.46+12350T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43869904 | ||||||
| chrX:43870408
|
C | CT | 40 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(37): Show | 40 | HG00735.hp1 HG02280.hp1 HG02280.hp2 others(37): Show |
intron_variant | MODIFIER | c.46+11845dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870408 | ||||||
| chrX:43870571
|
G | A | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+11683C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870571 | ||||||
| chrX:43870639
|
C | CA | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.46+11614dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870639 | ||||||
| chrX:43870712
|
A | G | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+11542T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870712 | ||||||
| chrX:43870769
|
TG | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0207 | 2 | HG00741.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.46+11484delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870769 | ||||||
| chrX:43870794
|
C | CA | 46 | a0001c0001t0001g0014a0001c0001t0001g0119a0001c0001t0001g0122others(43): Show | 46 | HG01099.hp1 HG01192.hp1 HG02145.hp1 others(43): Show |
intron_variant | MODIFIER | c.46+11459dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870794 | ||||||
| chrX:43870794
|
C | CAA | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00735.hp1 HG02056.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.46+11458_46+11459d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870794 | ||||||
| chrX:43870794
|
CA | C | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(12): Show | 15 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.46+11459delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870794 | ||||||
| chrX:43870794
|
CAA | C | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46+11458_46+11459d others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870794 | ||||||
| chrX:43870794
|
CAAAAA | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0207 | 2 | HG00741.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.46+11455_46+11459d others(7): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870794 | ||||||
| chrX:43870877
|
T | C | 45 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(42): Show | 45 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.46+11377A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870877 | ||||||
| chrX:43871015
|
G | A | 5 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+11239C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43871015 | ||||||
| chrX:43871700
|
A | G | 4 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+10554T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43871700 | ||||||
| chrX:43871801
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46+10453G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43871801 | ||||||
| chrX:43871870
|
G | A | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.46+10384C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43871870 | ||||||
| chrX:43872338
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46+9916T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43872338 | ||||||
| chrX:43872348
|
G | T | 2 | a0001c0002t0002g0211a0001c0002t0002g0212 | 2 | NA18747.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.46+9906C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43872348 | ||||||
| chrX:43872571
|
C | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+9683G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43872571 | ||||||
| chrX:43872900
|
A | AT | 1 | a0001c0001t0001g0014 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.46+9353dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43872900 | ||||||
| chrX:43872931
|
T | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+9323A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43872931 | ||||||
| chrX:43873049
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02572.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.46+9205A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43873049 | ||||||
| chrX:43873337
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.46+8917T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43873337 | ||||||
| chrX:43873482
|
G | T | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.46+8772C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43873482 | ||||||
| chrX:43873708
|
G | C | 40 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(37): Show | 40 | HG00735.hp1 HG02280.hp1 HG02280.hp2 others(37): Show |
intron_variant | MODIFIER | c.46+8546C>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43873708 | ||||||
| chrX:43873722
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.46+8532C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43873722 | ||||||
| chrX:43874550
|
T | C | 17 | a0001c0001t0001g0016a0001c0001t0001g0135a0001c0001t0001g0137others(14): Show | 17 | HG02523.hp2 HG03831.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.46+7704A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43874550 | ||||||
| chrX:43874574
|
T | C | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+7680A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43874574 | ||||||
| chrX:43874627
|
C | T | 2 | a0001c0002t0002g0203a0001c0002t0002g0208 | 2 | NA18957.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.46+7627G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43874627 | ||||||
| chrX:43874838
|
T | C | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+7416A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43874838 | ||||||
| chrX:43875254
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.46+7000T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875254 | ||||||
| chrX:43875260
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.46+6994C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875260 | ||||||
| chrX:43875585
|
T | C | 1 | a0001c0002t0002g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.46+6669A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875585 | ||||||
| chrX:43875647
|
CGTGGCCC others(6): Show |
C | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.46+6594_46+6606del others(13): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875647 | ||||||
| chrX:43875655
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.46+6599G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875655 | ||||||
| chrX:43875737
|
T | TGAC | 1 | a0001c0002t0002g0232 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.46+6514_46+6516dup others(3): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875737 | ||||||
| chrX:43875862
|
T | C | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+6392A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875862 | ||||||
| chrX:43875963
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.46+6291A>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875963 | ||||||
| chrX:43876413
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.46+5841C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43876413 | ||||||
| chrX:43876503
|
C | CA | 1 | a0001c0001t0001g0014 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.46+5750dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43876503 | ||||||
| chrX:43876680
|
T | C | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+5574A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43876680 | ||||||
| chrX:43876879
|
CAG | C | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+5373_46+5374del others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43876879 | ||||||
| chrX:43877446
|
G | A | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG00099.hp1 HG01071.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+4808C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43877446 | ||||||
| chrX:43877739
|
C | T | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+4515G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43877739 | ||||||
| chrX:43877795
|
G | T | 2 | a0001c0002t0002g0210a0003c0006t0002g0209 | 2 | NA18983.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.46+4459C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43877795 | ||||||
| chrX:43877860
|
A | C | 1 | a0001c0002t0002g0208 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.46+4394T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43877860 | ||||||
| chrX:43877874
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.46+4380G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43877874 | ||||||
| chrX:43878043
|
C | T | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+4211G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878043 | ||||||
| chrX:43878070
|
A | T | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+4184T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878070 | ||||||
| chrX:43878113
|
C | T | 5 | a0001c0003t0004g0185a0001c0003t0004g0186a0001c0003t0004g0187others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+4141G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878113 | ||||||
| chrX:43878329
|
G | A | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+3925C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878329 | ||||||
| chrX:43878342
|
A | G | 7 | a0001c0003t0004g0010a0001c0003t0006g0008a0001c0003t0006g0009others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+3912T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878342 | ||||||
| chrX:43878378
|
A | C | 1 | a0001c0001t0003g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.46+3876T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878378 | ||||||
| chrX:43878406
|
CT | C | 4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0197others(1): Show | 4 | HG01255.hp1 HG02071.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+3847delA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878406 | ||||||
| chrX:43878408
|
T | TGTGTG | 1 | a0001c0002t0002g0230 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.46+3845_46+3846ins others(5): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878408 | ||||||
| chrX:43878408
|
T | TTG | 1 | a0001c0001t0001g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.46+3844_46+3845dup others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878408 | ||||||
| chrX:43878408
|
T | TTGTG | 30 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0222others(27): Show | 30 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.46+3842_46+3845dup others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878408 | ||||||
| chrX:43878408
|
T | TTGTGTG | 7 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(4): Show | 7 | HG02280.hp1 HG03098.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+3840_46+3845dup others(6): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878408 | ||||||
| chrX:43878408
|
TTG | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0016others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.46+3844_46+3845del others(2): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878408 | ||||||
| chrX:43878408
|
TTGTG | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0199 | 2 | HG02723.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.46+3842_46+3845del others(4): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878408 | ||||||
| chrX:43878445
|
TG | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+3808delC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878445 | ||||||
| chrX:43878448
|
A | T | 4 | a0001c0003t0004g0010a0001c0004t0005g0011a0001c0004t0005g0012others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+3806T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878448 | ||||||
| chrX:43878483
|
A | G | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+3771T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878483 | ||||||
| chrX:43878608
|
T | C | 1 | a0001c0003t0010g0196 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.46+3646A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878608 | ||||||
| chrX:43878925
|
A | C | 3 | a0001c0003t0006g0008a0001c0003t0006g0009a0001c0003t0007g0001 | 3 | HG02280.hp2 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.46+3329T>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43878925 | ||||||
| chrX:43879076
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.46+3178C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43879076 | ||||||
| chrX:43879181
|
C | A | 26 | a0001c0001t0001g0222a0001c0002t0002g0203a0001c0002t0002g0208others(23): Show | 26 | HG02683.hp1 HG03017.hp1 HG03239.hp1 others(23): Show |
intron_variant | MODIFIER | c.46+3073G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43879181 | ||||||
| chrX:43879300
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.46+2954A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43879300 | ||||||
| chrX:43879328
|
G | T | 1 | a0001c0002t0002g0203 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.46+2926C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43879328 | ||||||
| chrX:43879716
|
T | G | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.46+2538A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43879716 | ||||||
| chrX:43880236
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.46+2018A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43880236 | ||||||
| chrX:43880585
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.46+1669C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43880585 | ||||||
| chrX:43880740
|
C | T | 7 | a0001c0003t0004g0010a0001c0003t0006g0008a0001c0003t0006g0009others(4): Show | 7 | HG02280.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.46+1514G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43880740 | ||||||
| chrX:43881204
|
G | GT | 1 | a0001c0001t0001g0007 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.46+1049dupA | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43881204 | ||||||
| chrX:43881325
|
G | A | 30 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(27): Show | 30 | HG00741.hp1 HG02683.hp1 HG03017.hp1 others(27): Show |
intron_variant | MODIFIER | c.46+929C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43881325 | ||||||
| chrX:43881533
|
C | T | 3 | a0001c0002t0002g0005a0001c0005t0001g0004a0001c0005t0001g0006 | 3 | HG00642.hp1 HG01081.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.46+721G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43881533 | ||||||
| chrX:43881569
|
A | AG | 1 | a0001c0001t0001g0003 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.46+684dupC | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43881569 | ||||||
| chrX:43881574
|
G | A | 2 | a0001c0002t0002g0231a0001c0002t0002g0232 | 2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.46+680C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43881574 | ||||||
| chrX:43881738
|
G | A | 1 | a0001c0004t0001g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46+516C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43881738 |