Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 233 | 44 | 49 | 99 | 9 | 30 | 81 | MAOB_chrX_43761610_43887450 | MAOB | MSNKC others(515): Show |
chrX | 43761610 | 43887450 |
| a0002 | 0/0 | 520 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | MSNKC others(515): Show |
chrX | 43761610 | 43887450 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1560 | 174 | 32 | 39 | 71 | 9 | 21 | MAOB_chrX_43761610_43887450 | MAOB | ATGAG others(1555): Show |
chrX | 43761610 | 43887450 | ||
| a0001c0002 | 0/0 | 1560 | 43 | 0 | 6 | 28 | 0 | 9 | MAOB_chrX_43761610_43887450 | MAOB | ATGAG others(1555): Show |
chrX | 43761610 | 43887450 | ||
| a0001c0003 | 0/0 | 1560 | 9 | 7 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | ATGAG others(1555): Show |
chrX | 43761610 | 43887450 | ||
| a0001c0004 | 0/0 | 1560 | 4 | 4 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | ATGAG others(1555): Show |
chrX | 43761610 | 43887450 | ||
| a0001c0005 | 0/0 | 1560 | 3 | 1 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | ATGAG others(1555): Show |
chrX | 43761610 | 43887450 | ||
| a0002c0006 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | ATGAG others(1555): Show |
chrX | 43761610 | 43887450 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2570 | 159 | 21 | 39 | 67 | 9 | 21 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0001t0003 | 0/0 | 2570 | 10 | 10 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0001t0008 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0001t0009 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0001t0011 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0001t0012 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0001t0013 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0002t0002 | 0/0 | 2570 | 43 | 0 | 6 | 28 | 0 | 9 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0003t0004 | 0/0 | 2570 | 5 | 3 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0003t0006 | 0/0 | 2570 | 2 | 2 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0003t0007 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0003t0010 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0004t0001 | 0/0 | 2570 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0004t0005 | 0/0 | 2570 | 3 | 3 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0001c0005t0001 | 0/0 | 2570 | 3 | 1 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| a0002c0006t0001 | 0/0 | 2570 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | AATAT others(2565): Show |
chrX | 43761610 | 43887450 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0123 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0136 | 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 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0174 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0034 | 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 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0003g0040 | 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 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0001t0013g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0062 | 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 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0166 | 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 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0207 | 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 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0003t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0004t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0004t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0005t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0001c0005t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| a0002c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0006 | EUR | GBR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00642 | hp1 | a0001 | c0005 | t0001 | g0012 | 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 | g0187 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01081 | hp1 | a0001 | c0005 | t0001 | g0171 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0013 | 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 | g0041 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01167 | hp1 | a0001 | c0003 | t0004 | g0184 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01169 | hp1 | a0001 | c0003 | t0004 | g0185 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0072 | 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 | g0152 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01891 | hp1 | a0001 | c0003 | t0004 | g0183 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02056 | hp1 | a0002 | c0006 | t0001 | g0129 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0079 | 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 | g0162 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | CDX | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0180 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02280 | hp2 | a0001 | c0003 | t0007 | g0010 | AFR | ACB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0061 | 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 | g0132 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0222 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02723 | hp1 | a0001 | c0003 | t0010 | g0191 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02809 | hp2 | a0001 | c0003 | t0006 | g0016 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02895 | hp1 | a0001 | c0004 | t0005 | g0002 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02897 | hp1 | a0001 | c0004 | t0005 | g0002 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02922 | hp1 | a0001 | c0005 | t0001 | g0014 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0223 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0182 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0015 | AFR | ESN | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03209 | hp1 | a0001 | c0004 | t0005 | g0018 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0210 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0017 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0215 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0214 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0212 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | BEB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0122 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHB | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0208 | 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 | g0177 | AFR | YRI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18945 | hp1 | a0001 | c0001 | t0013 | g0090 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18965 | hp1 | a0001 | c0001 | t0009 | g0093 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0032 | 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 | g0082 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0221 | 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 | g0206 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0172 | 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 | g0145 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0224 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0189 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19079 | hp1 | a0001 | c0001 | t0012 | g0031 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0217 | 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 | g0173 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | TSI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0065 | 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 | g0159 | AFR | MSL | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0154 | REF | REF | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0174 | REF | REF | MAOB_chrX_43761610_43887450 | MAOB | chrX | 43761610 | 43887450 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:43767568 | G | A | 1 | a0001c0002 | 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 | a0001c0003 a0001c0004 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 1 | a0001c0002t0002 | 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 | 6 | a0001c0002t0002 a0001c0003t0004 a0001c0003t0006 others(3): 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 | 6 | a0001c0002t0002 a0001c0003t0004 a0001c0003t0006 others(3): 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 | a0001c0003t0006 a0001c0003t0007 |
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 | 1 | a0001c0002t0002 | 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 | a0001c0001t0009 a0001c0003t0006 a0001c0003t0007 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:43767621 | A | G | 52 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0013 others(49): 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 | 47 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0013 others(44): 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 | a0001c0003t0010g0191 | 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 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0193 | 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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0177 a0001c0001t0001g0190 others(1): 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 | 87 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0022 others(84): 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 | a0001c0003t0004g0183 | 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 | a0001c0001t0003g0039 | 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 | a0001c0001t0001g0176 | 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 | a0001c0002t0002g0122 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
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:43770192 | G | T | 5 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0193 | 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 | 3 | a0001c0001t0001g0007 a0001c0001t0001g0190 a0001c0001t0011g0189 |
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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 47 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0013 others(44): 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0010g0191 | 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0107 | 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 | 48 | a0001c0001t0001g0042 a0001c0002t0002g0008 a0001c0002t0002g0009 others(45): 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0011g0189 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(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 | 47 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0013 others(44): 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:43773025 | C | T | 1 | a0001c0001t0001g0106 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | 32 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(29): 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 37 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(34): 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 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | 65 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0026 others(62): 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0010g0191 | 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 | 65 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0026 others(62): 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 | a0001c0001t0001g0030 a0001c0001t0001g0048 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0003g0036 a0001c0001t0003g0120 a0001c0001t0003g0121 |
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 | 38 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(35): 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0003g0034 | 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 | a0001c0001t0001g0110 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0006g0015 others(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:43775054 | TG | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0074 |
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 | a0001c0001t0001g0042 a0001c0001t0001g0065 a0001c0001t0001g0080 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0026 others(40): 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:43775145 | C | T | 8 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1138-382T>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43775654 | |||||||
| chrX:43775813 | C | T | 1 | a0001c0001t0001g0097 | 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 | a0001c0004t0001g0224 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 2 | a0001c0001t0001g0006 a0001c0001t0001g0152 |
3 | HG00099.hp1 HG01071.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1138-1158G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776430 | |||||||
| chrX:43776441 | A | G | 3 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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:43776559 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1138-1287A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 11/14 | chrX | 43776559 | |||||||
| chrX:43776751 | C | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0058 a0001c0001t0001g0059 |
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:43776899 | C | T | 11 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(8): 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0002t0002g0180 | 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 | a0001c0002t0002g0013 a0001c0002t0002g0062 a0001c0002t0002g0165 others(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 | a0001c0002t0002g0223 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0010g0191 | 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 | a0001c0003t0010g0191 | 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0002t0002g0209 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0162 |
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 | a0001c0001t0001g0109 a0001c0001t0001g0162 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0002t0002g0027 | 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 | a0001c0002t0002g0027 | 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 | 25 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(22): 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 | a0001c0002t0002g0164 a0001c0002t0002g0172 |
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 | a0001c0001t0001g0069 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0077 |
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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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:43779533 | A | G | 9 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 37 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(34): 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 | a0001c0001t0001g0102 a0001c0001t0001g0107 |
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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0002t0002g0187 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0002t0002g0203 a0001c0002t0002g0220 |
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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 8 | a0001c0002t0002g0009 a0001c0002t0002g0207 a0001c0002t0002g0208 others(5): 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 | a0001c0001t0001g0037 | 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0002t0002g0213 | 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 | a0001c0001t0001g0038 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 16 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0053 others(13): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0085 | 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0079 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0010g0191 | 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 | a0001c0002t0002g0203 a0001c0002t0002g0211 a0001c0002t0002g0218 others(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:43782279 | T | C | 3 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0010g0191 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0068 others(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 | a0001c0003t0010g0191 | 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 | a0001c0001t0001g0123 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 37 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(34): 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0003g0019 a0001c0001t0003g0125 |
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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0048 | 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0001t0001g0007 a0001c0001t0001g0190 a0001c0001t0011g0189 |
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 | a0001c0002t0002g0217 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0020 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0058 | 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 | a0001c0003t0010g0191 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0103 | 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 4 | a0001c0001t0001g0005 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): 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 | a0001c0001t0001g0023 a0001c0001t0001g0037 |
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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 11 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(8): 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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:43787659 | T | TATTTTTT others(24): Show |
5 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 11 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(8): 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 | a0001c0001t0011g0189 | 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0001t0001g0076 a0001c0001t0001g0126 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0188 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0010g0191 | 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 | 11 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0041 others(8): 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 37 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): 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 | a0001c0001t0001g0023 a0001c0001t0001g0037 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(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:43790625 | G | A | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0001t0012g0031 | 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 | a0001c0001t0001g0051 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.928+2119A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 8/14 | chrX | 43791300 | |||||||
| chrX:43791581 | C | T | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | 34 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(31): 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 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0068 others(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 | a0001c0003t0004g0183 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0200 | 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 | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): 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 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0143 |
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 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | 38 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(35): 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0032 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.769-231T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 7/14 | chrX | 43793809 | |||||||
| chrX:43794157 | T | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0176 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0123 | 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0004t0001g0224 | 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0002t0002g0180 | 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 | a0001c0001t0001g0188 | 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 | a0001c0002t0002g0223 | 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 | a0001c0002t0002g0204 | 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 |
26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0003t0010g0191 | 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 | a0001c0002t0002g0213 | 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 | a0001c0001t0001g0110 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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:43796348 | C | G | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0046 | 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 | a0001c0002t0002g0210 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0042 | 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 | a0001c0004t0001g0224 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0067 | 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 | a0001c0003t0010g0191 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0002t0002g0166 | 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 35 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(32): 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 | a0001c0001t0001g0042 | 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 | 36 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(33): 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 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0190 | 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 | 12 | a0001c0003t0004g0017 a0001c0003t0004g0182 a0001c0003t0004g0183 others(9): 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 | a0001c0001t0001g0188 | 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 | a0001c0005t0001g0012 a0001c0005t0001g0171 |
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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0003t0010g0191 | 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 | a0001c0002t0002g0212 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0188 | 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 | 67 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0026 others(64): 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 | a0001c0001t0001g0188 | 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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:43801126 | C | CT | 10 | a0001c0002t0002g0214 a0001c0003t0004g0017 a0001c0003t0004g0182 others(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:43801270 | T | C | 2 | a0001c0002t0002g0205 a0001c0002t0002g0209 |
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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0024 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.476+679T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 5/14 | chrX | 43801493 | |||||||
| chrX:43801903 | C | T | 37 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(34): 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:43801922 | C | T | 1 | a0001c0003t0010g0191 | 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 | 2 | a0001c0002t0002g0008 a0001c0002t0002g0221 |
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:43802030 | C | T | 2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
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:43802297 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0161 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0194 | 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0001t0001g0030 a0001c0001t0001g0048 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0150 | 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 | 12 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(9): 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 | 12 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(9): 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:43802825 | T | C | 1 | a0001c0002t0002g0213 | 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 | a0001c0002t0002g0214 | 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 | a0001c0001t0001g0156 | 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 | 1 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0141 a0001c0001t0001g0146 |
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:43804186 | G | A | 1 | a0001c0001t0001g0056 | 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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.280-1046C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43804450 | |||||||
| chrX:43804455 | A | AAGAGAG | 3 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | 8 | a0001c0002t0002g0009 a0001c0002t0002g0207 a0001c0002t0002g0208 others(5): 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 | a0001c0003t0004g0185 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0002t0002g0222 | 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 | a0001c0001t0001g0150 a0001c0001t0003g0034 a0001c0001t0003g0035 others(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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0002t0002g0217 | 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 | a0001c0002t0002g0204 | 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 | 41 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(38): 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 | a0001c0001t0001g0138 | 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 | a0001c0002t0002g0213 | 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 | a0001c0001t0013g0090 | 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 | 1 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0179 |
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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0002t0002g0166 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0096 |
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 | 4 | a0001c0001t0001g0005 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0002t0002g0210 | 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 | a0001c0002t0002g0210 | 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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | a0001c0003t0010g0191 | 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 | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0020 others(66): Show |
72 | HG00140.hp1 HG00621.hp1 HG01069.hp1 others(69): 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 | a0001c0001t0001g0022 a0001c0001t0001g0094 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0177 | 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 | CATCTAT | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(44): 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 | a0001c0001t0001g0084 a0001c0001t0001g0108 a0001c0001t0001g0117 |
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 | 5 | a0001c0001t0001g0007 a0001c0001t0001g0064 a0001c0001t0001g0188 others(2): 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 | a0001c0002t0002g0206 | 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 | a0001c0002t0002g0206 | 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 | a0001c0002t0002g0206 | 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 | TACAC | 3 | a0001c0002t0002g0205 a0001c0002t0002g0209 a0001c0002t0002g0213 |
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 | 17 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(14): 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 | a0001c0002t0002g0206 | 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 | 17 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(14): 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 | a0001c0002t0002g0205 a0001c0002t0002g0209 a0001c0002t0002g0213 |
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 | 21 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(18): 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 | a0001c0002t0002g0205 a0001c0002t0002g0206 a0001c0002t0002g0209 others(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 | a0001c0002t0002g0214 | 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 | a0001c0002t0002g0122 a0001c0002t0002g0198 a0001c0002t0002g0203 others(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 |
4 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(1): 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 | a0001c0002t0002g0222 | 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 | a0001c0002t0002g0223 | 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 | a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | 20 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(17): 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 | 22 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(19): 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 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0068 a0001c0003t0006g0015 |
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 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0002g0212 others(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 | a0001c0002t0002g0187 | 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 | a0001c0003t0004g0017 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0023 | 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | 11 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(8): 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 | a0001c0001t0013g0090 | 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 | a0001c0002t0002g0219 | 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 | a0001c0003t0010g0191 | 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 | 11 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(8): 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 | a0001c0001t0001g0095 | 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 | 15 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(12): 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 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0216 |
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 | 1 | a0001c0002t0002g0009 | 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 | a0001c0002t0002g0009 a0001c0002t0002g0187 a0001c0002t0002g0203 others(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 | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.280-6839delT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43810242 | |||||||
| chrX:43810242 | CAA | C | 19 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0107 others(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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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:43810702 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(35): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0162 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0002t0002g0207 a0001c0002t0002g0208 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | 62 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0026 others(59): 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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | 41 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(38): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0176 | 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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0094 | 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 | a0001c0004t0001g0224 | 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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | a0001c0003t0010g0191 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0179 |
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 | a0001c0001t0001g0042 | 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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | 37 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): 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 | a0001c0001t0001g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280-12438G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43815842 | |||||||
| chrX:43816676 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | a0001c0004t0001g0224 | 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 | a0001c0003t0010g0191 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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:43817118 | ATCT | A | 3 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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:43817368 | C | A | 2 | a0001c0001t0003g0019 a0001c0001t0003g0125 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0010g0191 | 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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0047 |
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 | a0001c0002t0002g0164 a0001c0002t0002g0168 a0001c0002t0002g0172 |
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 | 63 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0026 others(60): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0003g0019 | 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 | a0001c0001t0001g0177 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | a0001c0003t0010g0191 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 4 | a0001c0002t0002g0205 a0001c0003t0004g0017 a0001c0004t0005g0002 others(1): 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 | a0001c0001t0001g0157 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(39): 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 | a0001c0001t0001g0101 | 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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0193 | 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 | TCAC | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0072 | 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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0049 others(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 | CT | C | 36 | a0001c0001t0001g0079 a0001c0001t0001g0135 a0001c0001t0001g0157 others(33): 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:43823334 | G | A | 1 | a0001c0003t0010g0191 | 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 | 5 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0003t0004g0017 others(2): 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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0002t0002g0173 | 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 | a0001c0001t0001g0136 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | 26 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0115 others(23): 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0048 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0032 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(39): 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 | a0001c0001t0001g0063 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.279+14267A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824601 | |||||||
| chrX:43824763 | G | A | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 25 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0122 others(22): 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 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(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 | 25 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0122 others(22): 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 | a0001c0001t0001g0071 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.279+13870A>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43824998 | |||||||
| chrX:43825384 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0008g0011 | 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 | a0001c0003t0010g0191 | 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 | a0001c0002t0002g0173 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.279+12117G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 3/14 | chrX | 43826751 | |||||||
| chrX:43826951 | T | C | 26 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0009 others(23): 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 | a0001c0004t0001g0224 | 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 | a0001c0001t0003g0019 | 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 | a0001c0002t0002g0212 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0128 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | 4 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): 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 | a0001c0001t0001g0158 | 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 | 78 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0025 others(75): 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0077 others(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 | 27 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0009 others(24): 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
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 | a0001c0001t0001g0076 | 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 | a0001c0001t0003g0159 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): 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 | 37 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0127 others(34): 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 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0083 others(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 | 7 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0190 others(4): 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 | 1 | a0001c0004t0005g0002 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0042 | 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 | 26 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0009 others(23): 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 | a0001c0001t0001g0025 a0001c0001t0001g0195 |
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 | 31 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0188 others(28): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0067 | 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 | 5 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(2): 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 | a0001c0003t0010g0191 | 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 | a0001c0002t0002g0178 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0195 |
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 | 25 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0009 others(22): 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:43833717 | CA | C | 3 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0080 | 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 | a0001c0002t0002g0013 a0001c0005t0001g0012 a0001c0005t0001g0014 |
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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0032 | 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 | a0001c0004t0005g0018 | 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 | a0001c0002t0002g0205 a0001c0002t0002g0206 |
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 | a0001c0001t0001g0022 | 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 | a0001c0002t0002g0205 a0001c0002t0002g0206 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0141 a0001c0001t0001g0146 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0066 | 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 | a0001c0004t0001g0224 | 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 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(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 | 26 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0009 others(23): 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:43838392 | C | T | 26 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0009 others(23): 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 |
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:43839013 | C | T | 1 | a0001c0001t0001g0111 | 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:43839380 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142-375T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839380 | |||||||
| chrX:43839449 | T | C | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0101 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.142-624A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43839629 | |||||||
| chrX:43840053 | C | A | 2 | a0001c0001t0001g0065 a0001c0002t0002g0122 |
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 | a0001c0003t0004g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-1079T>C | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840084 | |||||||
| chrX:43840303 | T | A | 1 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.142-1457C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 2/14 | chrX | 43840462 | |||||||
| chrX:43840747 | T | C | 12 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0081 others(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 | 38 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0070 others(35): 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 | a0001c0002t0002g0207 a0001c0003t0004g0182 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0108 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0020 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0079 | 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 | 17 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0122 others(14): 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 | 26 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0009 others(23): 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 | a0001c0001t0001g0179 | 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 | a0001c0002t0002g0205 a0001c0002t0002g0206 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0003g0019 a0001c0001t0003g0125 |
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 | a0001c0002t0002g0205 a0001c0002t0002g0206 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0107 |
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 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(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 | a0001c0002t0002g0168 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0141 others(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 | TCA | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(32): Show |
36 | HG00609.hp1 HG00642.hp1 HG00738.hp1 others(33): 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 | 36 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(33): 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 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0109 others(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 | 9 | a0001c0001t0001g0054 a0001c0001t0001g0124 a0001c0003t0004g0017 others(6): 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 | a0001c0001t0001g0067 | 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 | 21 | a0001c0001t0001g0065 a0001c0002t0002g0008 a0001c0002t0002g0009 others(18): 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 | a0001c0002t0002g0203 a0001c0002t0002g0205 a0001c0002t0002g0206 others(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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0036 others(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 | a0001c0001t0003g0121 | 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 33 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0030 others(30): 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 | 38 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0186 others(35): 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:43845595 | G | A | 1 | a0001c0003t0010g0191 | 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 | 33 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0030 others(30): 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:43845615 | T | A | 1 | a0001c0001t0001g0072 | 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 | a0001c0002t0002g0209 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0072 | 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.47-2564A>G | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43846328 | |||||||
| chrX:43846973 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): 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 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0003t0010g0191 | 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 | 28 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(25): 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 | 37 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(34): 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 | a0001c0001t0001g0155 a0001c0001t0001g0160 |
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 | a0001c0003t0010g0191 | 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 | a0001c0001t0001g0152 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(39): 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0010g0191 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0104 | 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 | 28 | a0001c0001t0001g0030 a0001c0001t0001g0216 a0001c0002t0002g0008 others(25): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0153 | 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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | a0001c0001t0001g0201 | 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0094 a0001c0001t0001g0109 a0001c0001t0001g0162 others(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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | a0001c0001t0001g0075 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(39): 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 | a0001c0001t0001g0199 a0001c0001t0008g0011 |
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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0150 | 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 | 28 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(25): 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0022 | 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 | a0001c0002t0002g0217 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.47-9144C>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43852908 | |||||||
| chrX:43853129 | G | A | 1 | a0001c0001t0001g0105 | 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 | 33 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0032 others(30): 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 | CA | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0075 a0001c0001t0001g0085 others(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:43853278 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0106 | 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 | 12 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0082 others(9): 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:43853744 | C | T | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0106 | 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 | a0001c0003t0010g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-10510G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43854274 | |||||||
| chrX:43854828 | C | A | 1 | a0001c0001t0001g0037 | 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 | 37 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(34): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(39): 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0003g0159 | 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 | a0001c0002t0002g0214 | 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 | a0001c0001t0001g0042 | 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | 25 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(22): 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:43855495 | T | C | 1 | a0001c0001t0001g0123 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(39): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 4 | a0001c0001t0001g0005 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): 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 | a0001c0001t0001g0021 a0001c0001t0001g0106 a0001c0001t0001g0117 others(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 | 42 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(39): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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:43856049 | A | C | 1 | a0001c0002t0002g0215 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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:43856616 | T | C | 3 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0078 | 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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | 32 | a0001c0001t0001g0007 a0001c0001t0001g0107 a0001c0001t0001g0133 others(29): 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:43857084 | A | AAT | 10 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0148 a0001c0001t0001g0199 |
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 |
6 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0136 others(3): 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 | a0001c0001t0001g0135 a0001c0002t0002g0213 a0001c0002t0002g0214 others(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 | a0001c0002t0002g0207 a0001c0002t0002g0223 |
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 | a0001c0001t0001g0163 | 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 | a0001c0002t0002g0208 | 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 | a0001c0001t0001g0137 a0001c0002t0002g0134 |
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 | a0001c0001t0008g0011 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0201 a0001c0003t0004g0183 |
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 | a0001c0001t0001g0037 a0001c0001t0001g0075 |
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 | a0001c0002t0002g0198 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0003g0019 | 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 | a0001c0001t0003g0034 | 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 | a0001c0001t0001g0177 a0001c0001t0003g0120 |
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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0150 a0001c0001t0003g0035 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0160 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0044 |
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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0006 | 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 | 2 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0056 a0001c0001t0003g0121 |
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 | a0001c0001t0001g0055 a0001c0001t0003g0125 |
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 | a0001c0001t0001g0065 | 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 | 4 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0030 others(1): Show |
4 | HG00099.hp1 HG01099.hp1 HG01175.hp1 others(1): 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 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0066 | 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 | 5 | a0001c0002t0002g0204 a0001c0002t0002g0205 a0001c0002t0002g0206 others(2): 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 | TATAGAGA others(3): Show |
T | 1 | a0001c0001t0003g0036 | 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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0072 |
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 | a0001c0001t0001g0045 | 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 | 12 | a0001c0001t0001g0023 a0001c0001t0001g0175 a0001c0002t0002g0122 others(9): 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 | a0001c0001t0001g0021 a0001c0001t0001g0049 |
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 | TATATATA others(5): Show |
1 | a0001c0003t0006g0016 | 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 | a0001c0003t0006g0015 | 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 | a0001c0001t0001g0197 | 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 | a0001c0003t0007g0010 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0050 a0001c0001t0001g0074 others(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 | 8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(5): 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 | a0001c0001t0001g0063 a0001c0001t0001g0131 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0048 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0153 a0001c0001t0003g0040 |
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 | a0001c0001t0001g0192 | 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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0020 others(71): 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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(72): 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 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0020 others(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 | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): 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 | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): 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 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0079 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0145 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0192 |
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 | a0001c0001t0001g0145 | 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 | a0001c0002t0002g0013 a0001c0003t0010g0191 a0001c0005t0001g0014 |
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 | a0001c0005t0001g0012 | 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 | 3 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0123 a0001c0001t0001g0186 others(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 | a0001c0002t0002g0198 a0001c0002t0002g0206 a0001c0002t0002g0208 |
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:43857156 | G | GA | 2 | a0001c0001t0001g0216 a0001c0002t0002g0205 |
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 | a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0011g0189 a0001c0003t0004g0184 a0001c0003t0004g0185 |
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 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
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 | a0001c0001t0001g0216 a0001c0002t0002g0198 a0001c0002t0002g0205 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0099 others(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 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0211 others(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 | a0001c0001t0001g0216 a0001c0002t0002g0198 a0001c0002t0002g0205 others(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 | a0001c0001t0001g0177 a0001c0002t0002g0187 a0001c0003t0004g0182 others(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 | a0001c0001t0001g0216 a0001c0002t0002g0198 a0001c0002t0002g0203 others(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 | GAGAGAAG others(4): Show |
1 | a0001c0002t0002g0219 | 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 | a0001c0002t0002g0209 | 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 | a0001c0001t0001g0162 a0001c0003t0006g0015 a0001c0003t0006g0016 |
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 | 16 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0123 others(13): 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 | AAGAAGAA others(3): Show |
4 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0210 others(1): 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 | a0001c0002t0002g0215 | 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 | a0001c0002t0002g0213 a0001c0002t0002g0218 a0001c0002t0002g0223 |
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 | a0001c0002t0002g0207 a0001c0002t0002g0217 |
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 | 17 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0038 others(14): 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 | a0001c0002t0002g0203 a0001c0002t0002g0205 a0001c0002t0002g0208 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0066 others(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 | a0001c0003t0006g0015 a0001c0003t0006g0016 |
2 | HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.47-13407dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43857170 | |||||||
| chrX:43857368 | T | C | 25 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(22): 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 | a0001c0001t0001g0202 | 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 | a0001c0003t0010g0191 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0177 |
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 | a0001c0001t0001g0163 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0002t0002g0178 | 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0162 | 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 | a0001c0002t0002g0013 a0001c0005t0001g0012 a0001c0005t0001g0014 |
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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0108 | 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 | a0001c0002t0002g0210 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0150 a0001c0001t0003g0034 others(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 | a0001c0001t0003g0159 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0109 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | 7 | a0001c0003t0004g0017 a0001c0003t0006g0015 a0001c0003t0006g0016 others(4): 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 | 7 | a0001c0003t0004g0017 a0001c0003t0006g0015 a0001c0003t0006g0016 others(4): 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 | a0001c0001t0001g0037 a0001c0001t0001g0079 a0001c0001t0001g0116 others(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 | a0001c0003t0004g0182 a0001c0003t0004g0184 a0001c0003t0004g0185 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 |
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 | a0001c0003t0007g0010 | 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 | 36 | a0001c0001t0001g0007 a0001c0001t0001g0076 a0001c0001t0001g0126 others(33): 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 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0177 |
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 | a0001c0001t0001g0022 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0026 | 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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | a0001c0001t0001g0133 a0001c0001t0001g0145 a0001c0001t0001g0147 |
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 | 7 | a0001c0002t0002g0009 a0001c0002t0002g0207 a0001c0002t0002g0208 others(4): 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:43862871 | A | G | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0012g0031 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0110 | 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 1 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0144 | 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 | 9 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(6): 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 | a0001c0001t0001g0023 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46+17196C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43865058 | |||||||
| chrX:43865785 | CT | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0111 a0001c0001t0001g0112 others(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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | a0001c0001t0001g0150 a0001c0001t0003g0034 a0001c0001t0003g0035 others(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 | a0001c0003t0006g0016 | 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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0077 | 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 | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0022 others(119): 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 | a0001c0003t0004g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.46+14638G>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43867616 | |||||||
| chrX:43868362 | C | T | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | 2 | a0001c0002t0002g0008 a0001c0002t0002g0221 |
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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0146 | 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 | 14 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(11): 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 | a0001c0001t0001g0116 a0001c0001t0001g0128 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0119 a0001c0001t0001g0156 |
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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | 41 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(38): 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 | a0001c0001t0001g0032 a0001c0001t0012g0031 |
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 | a0001c0001t0001g0030 | 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 | 36 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(33): 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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:43870712 | A | G | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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:43870794 | C | CA | 41 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0123 others(38): Show |
45 | HG01099.hp1 HG01192.hp1 HG02145.hp1 others(42): Show |
intron_variant | MODIFIER | c.46+11459dupT | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43870794 | |||||||
| chrX:43870794 | C | CAA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(4): 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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:43870877 | T | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(38): 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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | a0001c0001t0001g0023 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0023 | 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 | a0001c0002t0002g0207 a0001c0002t0002g0208 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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:43872931 | T | C | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0022 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | 36 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(33): 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0133 a0001c0001t0001g0135 others(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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | a0001c0002t0002g0198 a0001c0002t0002g0204 |
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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0149 | 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 | a0001c0002t0002g0178 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.46+6599G>A | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43875655 | |||||||
| chrX:43875862 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.46+5841C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43876413 | |||||||
| chrX:43876680 | T | C | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0001t0001g0006 a0001c0001t0001g0152 a0001c0001t0001g0153 |
4 | HG00099.hp1 HG01071.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+4808C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43877446 | |||||||
| chrX:43877739 | C | T | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | a0001c0002t0002g0205 a0001c0002t0002g0206 |
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 | a0001c0002t0002g0204 | 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 | a0001c0001t0001g0020 | 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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | 6 | a0001c0001t0001g0007 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): 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 | a0001c0003t0004g0182 a0001c0003t0004g0183 a0001c0003t0004g0184 others(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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | 6 | a0001c0003t0004g0017 a0001c0003t0006g0015 a0001c0003t0006g0016 others(3): 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 | a0001c0001t0003g0019 | 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 | a0001c0001t0001g0179 a0001c0001t0001g0181 a0001c0001t0001g0192 others(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 | TTGTG | 29 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0216 others(26): 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 | 5 | a0001c0001t0001g0007 a0001c0001t0001g0190 a0001c0001t0011g0189 others(2): 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 | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): 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:43878445 | TG | T | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 3 | a0001c0003t0004g0017 a0001c0004t0005g0002 a0001c0004t0005g0018 |
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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | a0001c0003t0010g0191 | 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 | a0001c0003t0006g0015 a0001c0003t0006g0016 a0001c0003t0007g0010 |
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 | a0001c0001t0001g0192 | 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 | 24 | a0001c0001t0001g0216 a0001c0002t0002g0008 a0001c0002t0002g0009 others(21): 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 | a0001c0001t0001g0193 | 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 | a0001c0002t0002g0198 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
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 | 6 | a0001c0003t0004g0017 a0001c0003t0006g0015 a0001c0003t0006g0016 others(3): 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:43881325 | G | A | 28 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(25): 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 | a0001c0002t0002g0013 a0001c0005t0001g0012 a0001c0005t0001g0014 |
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:43881574 | G | A | 2 | a0001c0002t0002g0222 a0001c0002t0002g0223 |
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 | a0001c0004t0001g0224 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46+516C>T | MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | 43881738 |