Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4168 |
|---|---|
| ensemblid | ENSG00000101977.22 |
| hgncid | 6940 |
| symbol | MCF2 |
| name | MCF.2 cell line derived transforming sequence |
| refseq_nuc | NM_001171876.2 |
| refseq_prot | NP_001165347.1 |
| ensembl_nuc | ENST00000519895.6 |
| ensembl_prot | ENSP00000430276.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 139581770 |
| end | 139708167 |
| strand | - |
| ver | v1.2 |
| region | chrX:139581770-139708167 |
| region5000 | chrX:139576770-139713167 |
| regionname0 | MCF2_chrX_139581770_139708167 |
| regionname5000 | MCF2_chrX_139576770_139713167 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1001 | 243 | 67 | 44 | 101 | 7 | 22 | 80 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0002 | 0/0 | 1001 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0003 | 0/0 | 1002 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0004 | 0/0 | 1001 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0005 | 0/0 | 1001 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3006 | 185 | 54 | 30 | 79 | 4 | 17 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0002 | 0/0 | 3006 | 29 | 10 | 4 | 15 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0003 | 0/1 | 3006 | 24 | 0 | 10 | 5 | 3 | 5 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0004 | 0/0 | 3006 | 3 | 3 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0005 | 0/0 | 3006 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0006 | 0/0 | 3006 | 2 | 0 | 0 | 2 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0007 | 0/0 | 3009 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0008 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0009 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| c0010 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 808 | 237 | 65 | 44 | 97 | 7 | 22 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| t0002 | 0/0 | 808 | 5 | 0 | 0 | 5 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| t0003 | 0/0 | 808 | 3 | 3 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| t0004 | 0/0 | 808 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| t0005 | 0/0 | 808 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| t0006 | 0/0 | 808 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| t0007 | 0/0 | 808 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3006 | 185 | 54 | 30 | 79 | 4 | 17 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0002 | 0/0 | 3006 | 29 | 10 | 4 | 15 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0003 | 0/1 | 3006 | 24 | 0 | 10 | 5 | 3 | 5 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0005 | 0/0 | 3006 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0006 | 0/0 | 3006 | 2 | 0 | 0 | 2 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0010 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0002c0004 | 0/0 | 3006 | 3 | 3 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0003c0007 | 0/0 | 3009 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0004c0009 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0005c0008 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3813 | 176 | 50 | 30 | 74 | 4 | 17 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0001t0002 | 0/0 | 3813 | 5 | 0 | 0 | 5 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0001t0004 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0001t0005 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0001t0006 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0001t0007 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0002t0001 | 0/0 | 3813 | 29 | 10 | 4 | 15 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0003t0001 | 0/1 | 3813 | 24 | 0 | 10 | 5 | 3 | 5 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0005t0001 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0006t0001 | 0/0 | 3813 | 2 | 0 | 0 | 2 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0001c0010t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0002c0004t0003 | 0/0 | 3813 | 3 | 3 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0003c0007t0001 | 0/0 | 3816 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0004c0009t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| a0005c0008t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | copy fasta | chrX | 139576770 | 139713167 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0010t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0002c0004t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0002c0004t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0002c0004t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0003c0007t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0004c0009t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0005c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0051 | EUR | GBR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0105 | EUR | GBR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0064 | EUR | FIN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0138 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0037 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0246 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0080 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0197 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0114 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01884 | hp1 | a0002 | c0004 | t0003 | g0165 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01891 | hp2 | a0002 | c0004 | t0003 | g0166 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02451 | hp2 | a0005 | c0008 | t0001 | g0153 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02630 | hp2 | a0002 | c0004 | t0003 | g0189 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0116 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03139 | hp1 | a0001 | c0010 | t0001 | g0125 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03225 | hp1 | a0004 | c0009 | t0001 | g0024 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0143 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0098 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0077 | SAS | STU | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0025 | SAS | BEB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | YRI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0154 | AFR | YRI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18953 | hp1 | a0001 | c0006 | t0001 | g0223 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18985 | hp1 | a0003 | c0007 | t0001 | g0026 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19001 | hp2 | a0001 | c0006 | t0001 | g0224 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | GIH | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0137 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0152 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | USA | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | USA | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | USA | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0167 | AFR | LWK | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0185 | REF | REF | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0170 | REF | REF | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| 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:139582493
|
G | A | 1 | a0005 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.2984C>T | p.Ser995Leu | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 29/29 | 3090/3813 | 2984/3006 | 995/1001 | chrX | 139582493 | ||
| chrX:139582502
|
C | T | 1 | a0004 | 1 | HG03225.hp1 | missense_variant&splice_region_variant | MODERATE | c.2975G>A | p.Arg992Lys | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 29/29 | 3081/3813 | 2975/3006 | 992/1001 | chrX | 139582502 | ||
| chrX:139587771
|
G | GGT | 1 | a0003 | 1 | NA18985.hp1 | frameshift_variant | HIGH | c.2694_2695insAC | p.Gln899fs | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/29 | 2800/3813 | 2694/3006 | 898/1001 | chrX | 139587771 | ||
| chrX:139587779
|
C | CT | 1 | a0003 | 1 | NA18985.hp1 | frameshift_variant | HIGH | c.2686dupA | p.Arg896fs | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/29 | 2792/3813 | 2686/3006 | 896/1001 | chrX | 139587779 | ||
| chrX:139589842
|
A | G | 1 | a0002 | 3 | HG01884.hp1 HG01891.hp2 HG02630.hp2 |
missense_variant | MODERATE | c.2591T>C | p.Ile864Thr | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/29 | 2697/3813 | 2591/3006 | 864/1001 | chrX | 139589842 |
| 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:139596585
|
G | A | 1 | a0001c0002 | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
synonymous_variant | LOW | c.2469C>T | p.Asp823Asp | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/29 | 2575/3813 | 2469/3006 | 823/1001 | chrX | 139596585 | ||
| chrX:139597553
|
T | A | 2 | a0001c0003a0004c0009 | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
synonymous_variant | LOW | c.2190A>T | p.Gly730Gly | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/29 | 2296/3813 | 2190/3006 | 730/1001 | chrX | 139597553 | ||
| chrX:139602418
|
G | A | 1 | a0001c0010 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.2052C>T | p.Cys684Cys | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/29 | 2158/3813 | 2052/3006 | 684/1001 | chrX | 139602418 | ||
| chrX:139632380
|
G | A | 1 | a0001c0006 | 2 | NA18953.hp1 NA19001.hp2 |
synonymous_variant | LOW | c.306C>T | p.Asp102Asp | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/29 | 412/3813 | 306/3006 | 102/1001 | chrX | 139632380 | ||
| chrX:139632389
|
C | T | 1 | a0001c0005 | 2 | HG02109.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.297G>A | p.Thr99Thr | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/29 | 403/3813 | 297/3006 | 99/1001 | chrX | 139632389 |
| 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:139581830
|
T | C | 1 | a0001c0001t0005 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*641A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 29/29 | 641 | chrX | 139581830 | |||||
| chrX:139581854
|
T | G | 1 | a0001c0001t0006 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 29/29 | 617 | chrX | 139581854 | |||||
| chrX:139581961
|
C | T | 1 | a0001c0001t0002 | 5 | HG00621.hp1 NA18995.hp1 NA19012.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*510G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 29/29 | 510 | chrX | 139581961 | |||||
| chrX:139581964
|
T | C | 1 | a0001c0001t0007 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*507A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 29/29 | 507 | chrX | 139581964 | |||||
| chrX:139582164
|
C | T | 1 | a0001c0001t0004 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 29/29 | 307 | chrX | 139582164 | |||||
| chrX:139582456
|
G | C | 1 | a0002c0004t0003 | 3 | HG01884.hp1 HG01891.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*15C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 29/29 | 15 | chrX | 139582456 |
| 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:139582695
|
G | GT | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2974-193dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139582695 | ||||||
| chrX:139582781
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2974-278T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139582781 | ||||||
| chrX:139582820
|
A | C | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(3): Show | 6 | HG01123.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2974-317T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139582820 | ||||||
| chrX:139583066
|
C | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2974-563G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583066 | ||||||
| chrX:139583145
|
T | C | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(26): Show | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.2974-642A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583145 | ||||||
| chrX:139583398
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0211 | 3 | HG02647.hp1 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2974-895T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583398 | ||||||
| chrX:139583473
|
G | A | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2974-970C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583473 | ||||||
| chrX:139583539
|
G | A | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2974-1036C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583539 | ||||||
| chrX:139583638
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0161others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2974-1135G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583638 | ||||||
| chrX:139583651
|
A | G | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2974-1148T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583651 | ||||||
| chrX:139583698
|
A | G | 97 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(94): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.2974-1195T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583698 | ||||||
| chrX:139583796
|
CAA | C | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2973+1268_2973+126 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583796 | ||||||
| chrX:139583855
|
TTGGGAAC | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2973+1204_2973+121 others(11): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139583855 | ||||||
| chrX:139584128
|
C | CA | 7 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0144others(4): Show | 7 | HG01496.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2973+937_2973+938i others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
C | CT | 29 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0027others(26): Show | 29 | HG00438.hp1 HG00673.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2973+937dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
C | CTT | 2 | a0001c0002t0001g0151a0003c0007t0001g0026 | 2 | HG02965.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2973+936_2973+937d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
C | CTTT | 4 | a0001c0002t0001g0015a0001c0002t0001g0155a0001c0002t0001g0156others(1): Show | 4 | HG03209.hp1 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2973+935_2973+937d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
C | CTTTT | 1 | a0001c0002t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2973+934_2973+937d others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
C | CTTTTT | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2973+933_2973+937d others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
CT | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0074others(4): Show | 7 | HG02109.hp1 HG02809.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.2973+937delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
CTT | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0001t0001g0194 | 3 | HG01243.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2973+936_2973+937d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
CTTTT | C | 4 | a0001c0002t0001g0218a0002c0004t0003g0165a0002c0004t0003g0166others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2973+934_2973+937d others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584128
|
CTTTTT | C | 21 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(18): Show | 21 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.2973+933_2973+937d others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584128 | ||||||
| chrX:139584129
|
T | A | 5 | a0001c0001t0001g0142a0001c0001t0001g0158a0001c0001t0001g0162others(2): Show | 5 | HG01261.hp1 HG02615.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2973+937A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584129 | ||||||
| chrX:139584130
|
T | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0145a0001c0001t0001g0175others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2973+936A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584130 | ||||||
| chrX:139584131
|
T | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0001t0001g0194 | 3 | HG01243.hp1 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2973+935A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584131 | ||||||
| chrX:139584201
|
T | A | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2973+865A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584201 | ||||||
| chrX:139584411
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2973+655A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584411 | ||||||
| chrX:139584490
|
C | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2973+576G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584490 | ||||||
| chrX:139584498
|
T | C | 1 | a0001c0002t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2973+568A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584498 | ||||||
| chrX:139584676
|
C | T | 3 | a0002c0004t0003g0165a0002c0004t0003g0166a0002c0004t0003g0189 | 3 | HG01884.hp1 HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2973+390G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584676 | ||||||
| chrX:139584849
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2973+217G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 28/28 | chrX | 139584849 | ||||||
| chrX:139585293
|
C | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0030others(33): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.2861-115G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139585293 | ||||||
| chrX:139585381
|
TCTAA | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2861-207_2861-204d others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139585381 | ||||||
| chrX:139585414
|
C | CA | 1 | a0001c0001t0001g0060 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2861-237dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139585414 | ||||||
| chrX:139585468
|
G | A | 1 | a0001c0002t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2861-290C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139585468 | ||||||
| chrX:139585623
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2861-445A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139585623 | ||||||
| chrX:139585871
|
C | A | 1 | a0001c0002t0001g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2860+507G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139585871 | ||||||
| chrX:139586037
|
T | A | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860+341A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139586037 | ||||||
| chrX:139586167
|
T | G | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2860+211A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139586167 | ||||||
| chrX:139586272
|
A | C | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2860+106T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 27/28 | chrX | 139586272 | ||||||
| chrX:139586568
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2751-81A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139586568 | ||||||
| chrX:139586575
|
CA | C | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2751-89delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139586575 | ||||||
| chrX:139586599
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2751-112A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139586599 | ||||||
| chrX:139586927
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0161 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2751-440G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139586927 | ||||||
| chrX:139586952
|
C | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2751-465G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139586952 | ||||||
| chrX:139587078
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2751-591A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139587078 | ||||||
| chrX:139587160
|
T | C | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2750+556A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139587160 | ||||||
| chrX:139587371
|
AC | A | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2750+344delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139587371 | ||||||
| chrX:139587414
|
G | GA | 7 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(4): Show | 7 | HG01123.hp2 HG01884.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2750+301dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139587414 | ||||||
| chrX:139587425
|
C | T | 1 | a0001c0003t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2750+291G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139587425 | ||||||
| chrX:139587479
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2750+237A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139587479 | ||||||
| chrX:139587481
|
T | C | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2750+235A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139587481 | ||||||
| chrX:139587570
|
C | G | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2750+146G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 26/28 | chrX | 139587570 | ||||||
| chrX:139587848
|
GC | G | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2678-61delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139587848 | ||||||
| chrX:139587858
|
T | TTC | 2 | a0001c0001t0001g0129a0001c0001t0001g0147 | 2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2678-72_2678-71dup others(2): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139587858 | ||||||
| chrX:139587867
|
T | TCA | 4 | a0001c0001t0001g0063a0001c0001t0001g0136a0001c0001t0001g0210others(1): Show | 4 | HG01099.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2678-81_2678-80dup others(2): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139587867 | ||||||
| chrX:139587867
|
TCA | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2678-81_2678-80del others(2): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139587867 | ||||||
| chrX:139587867
|
TCACACA | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2678-85_2678-80del others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139587867 | ||||||
| chrX:139587869
|
A | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0135a0001c0001t0001g0140others(14): Show | 17 | HG01243.hp1 HG01261.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.2678-81T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139587869 | ||||||
| chrX:139588009
|
G | GT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2678-222dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139588009 | ||||||
| chrX:139588060
|
C | CG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2678-273dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139588060 | ||||||
| chrX:139588095
|
T | TG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2677+264dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139588095 | ||||||
| chrX:139588166
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2677+194A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139588166 | ||||||
| chrX:139588276
|
A | AT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2677+83dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139588276 | ||||||
| chrX:139588284
|
G | GA | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2677+75dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139588284 | ||||||
| chrX:139588504
|
A | AT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-67dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588504 | ||||||
| chrX:139588530
|
A | AG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-93_2599-92ins others(1): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588530 | ||||||
| chrX:139588549
|
T | TA | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-112dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588549 | ||||||
| chrX:139588566
|
C | CT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-129dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588566 | ||||||
| chrX:139588572
|
C | T | 1 | a0001c0003t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2599-134G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588572 | ||||||
| chrX:139588573
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2599-135C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588573 | ||||||
| chrX:139588581
|
G | GT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-144dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588581 | ||||||
| chrX:139588644
|
A | AT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-207dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588644 | ||||||
| chrX:139588681
|
T | TG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-244dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588681 | ||||||
| chrX:139588683
|
G | T | 9 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0142others(6): Show | 9 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2599-245C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588683 | ||||||
| chrX:139588697
|
G | GC | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-260dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588697 | ||||||
| chrX:139588743
|
T | TCTA | 11 | a0001c0001t0001g0018a0001c0001t0001g0161a0001c0001t0001g0163others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2599-308_2599-306d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588743 | ||||||
| chrX:139588743
|
T | TCTACTA | 3 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0174 | 3 | HG03209.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2599-311_2599-306d others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588743 | ||||||
| chrX:139588743
|
TCTA | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(28): Show | 32 | HG00099.hp2 HG00408.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.2599-308_2599-306d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588743 | ||||||
| chrX:139588743
|
TCTACTA | T | 29 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0020others(26): Show | 29 | HG00735.hp1 HG01106.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2599-311_2599-306d others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588743 | ||||||
| chrX:139588746
|
A | G | 1 | a0001c0002t0001g0218 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2599-308T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588746 | ||||||
| chrX:139588759
|
C | A | 28 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 28 | HG00609.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2599-321G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588759 | ||||||
| chrX:139588759
|
C | CTAA | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2599-322_2599-321i others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588759 | ||||||
| chrX:139588762
|
C | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(53): Show | 56 | HG00609.hp1 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.2599-324G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588762 | ||||||
| chrX:139588762
|
C | CTAA | 31 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(28): Show | 32 | HG00099.hp2 HG00408.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.2599-327_2599-325d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588762 | ||||||
| chrX:139588762
|
C | CTAATAA | 29 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0020others(26): Show | 29 | HG00735.hp1 HG01106.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.2599-330_2599-325d others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588762 | ||||||
| chrX:139588762
|
CTAA | C | 11 | a0001c0001t0001g0018a0001c0001t0001g0161a0001c0001t0001g0163others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2599-327_2599-325d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588762 | ||||||
| chrX:139588762
|
CTAATAA | C | 3 | a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0174 | 3 | HG03209.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2599-330_2599-325d others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588762 | ||||||
| chrX:139588765
|
A | C | 9 | a0001c0001t0001g0023a0001c0001t0001g0164a0001c0001t0001g0172others(6): Show | 9 | HG01175.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2599-327T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588765 | ||||||
| chrX:139588768
|
A | C | 2 | a0001c0002t0001g0143a0001c0003t0001g0025 | 2 | HG03453.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2599-330T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588768 | ||||||
| chrX:139588835
|
T | TG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-398dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588835 | ||||||
| chrX:139588844
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2599-406G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588844 | ||||||
| chrX:139588929
|
C | CA | 12 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0204others(9): Show | 12 | HG01934.hp1 HG02723.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.2599-492dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588929 | ||||||
| chrX:139588929
|
CA | C | 3 | a0001c0001t0001g0131a0001c0002t0001g0196a0001c0002t0001g0198 | 3 | HG01069.hp1 HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2599-492delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588929 | ||||||
| chrX:139588941
|
A | C | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-503T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588941 | ||||||
| chrX:139588956
|
G | GC | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-519dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588956 | ||||||
| chrX:139588973
|
A | T | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(26): Show | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.2599-535T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588973 | ||||||
| chrX:139588992
|
CTG | C | 1 | a0001c0002t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2599-556_2599-555d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588992 | ||||||
| chrX:139589057
|
A | C | 2 | a0001c0002t0001g0221a0001c0002t0001g0222 | 2 | NA18990.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.2599-619T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139589057 | ||||||
| chrX:139589096
|
C | CT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-659dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139589096 | ||||||
| chrX:139589180
|
G | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0007g0068 | 3 | HG02055.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2598+655C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139589180 | ||||||
| chrX:139589186
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2598+649A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139589186 | ||||||
| chrX:139589417
|
A | AG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2598+417dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139589417 | ||||||
| chrX:139589430
|
T | C | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2598+405A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139589430 | ||||||
| chrX:139589711
|
TA | T | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2598+123delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139589711 | ||||||
| chrX:139589958
|
C | A | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2506-31G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139589958 | ||||||
| chrX:139590068
|
G | A | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(26): Show | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.2506-141C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590068 | ||||||
| chrX:139590085
|
C | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2506-158G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590085 | ||||||
| chrX:139590138
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0183 | 2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2506-211G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590138 | ||||||
| chrX:139590202
|
C | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0161others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2506-275G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590202 | ||||||
| chrX:139590403
|
G | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2506-476C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590403 | ||||||
| chrX:139590468
|
T | TA | 4 | a0001c0002t0001g0235a0002c0004t0003g0165a0002c0004t0003g0166others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2506-542dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590468 | ||||||
| chrX:139590468
|
T | TAA | 18 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(15): Show | 18 | HG00408.hp1 HG01175.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.2506-543_2506-542d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590468 | ||||||
| chrX:139590468
|
TA | T | 1 | a0001c0001t0001g0131 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2506-542delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590468 | ||||||
| chrX:139590476
|
A | AAT | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2506-550_2506-549i others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590476 | ||||||
| chrX:139590476
|
A | AT | 8 | a0001c0001t0001g0018a0001c0001t0001g0161a0001c0002t0001g0015others(5): Show | 8 | HG02145.hp1 HG02615.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2506-550_2506-549i others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590476 | ||||||
| chrX:139590476
|
A | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0117 | 2 | NA18944.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2506-549T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590476 | ||||||
| chrX:139590531
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2506-604G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590531 | ||||||
| chrX:139590536
|
G | A | 31 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0159others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.2506-609C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590536 | ||||||
| chrX:139590549
|
CTTCCTTA | C | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2506-629_2506-623d others(9): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590549 | ||||||
| chrX:139590628
|
A | G | 97 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(94): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.2506-701T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590628 | ||||||
| chrX:139590640
|
C | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2506-713G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590640 | ||||||
| chrX:139590917
|
C | A | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2506-990G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590917 | ||||||
| chrX:139591209
|
A | G | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2506-1282T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591209 | ||||||
| chrX:139591501
|
A | T | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2506-1574T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591501 | ||||||
| chrX:139591635
|
G | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2506-1708C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591635 | ||||||
| chrX:139591671
|
CA | C | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2506-1745delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591671 | ||||||
| chrX:139591715
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0136 | 2 | HG01258.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2506-1788G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591715 | ||||||
| chrX:139591746
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2506-1819G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591746 | ||||||
| chrX:139591897
|
T | TA | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2506-1971dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591897 | ||||||
| chrX:139591969
|
G | T | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(26): Show | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.2506-2042C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591969 | ||||||
| chrX:139591990
|
C | G | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2506-2063G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139591990 | ||||||
| chrX:139592123
|
T | G | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(26): Show | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.2506-2196A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139592123 | ||||||
| chrX:139592180
|
T | G | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2506-2253A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139592180 | ||||||
| chrX:139592184
|
CATT | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2506-2260_2506-225 others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139592184 | ||||||
| chrX:139592342
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2506-2415A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139592342 | ||||||
| chrX:139592735
|
C | G | 1 | a0001c0001t0001g0045 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2506-2808G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139592735 | ||||||
| chrX:139593258
|
G | A | 9 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(6): Show | 9 | HG01256.hp1 HG01515.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.2505+3291C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139593258 | ||||||
| chrX:139593416
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+3133G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139593416 | ||||||
| chrX:139593512
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2505+3037T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139593512 | ||||||
| chrX:139593735
|
C | T | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(3): Show | 6 | HG02965.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2505+2814G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139593735 | ||||||
| chrX:139593742
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2505+2807G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139593742 | ||||||
| chrX:139593777
|
C | G | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+2772G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139593777 | ||||||
| chrX:139593928
|
A | G | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2505+2621T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139593928 | ||||||
| chrX:139594015
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2505+2534G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594015 | ||||||
| chrX:139594099
|
T | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+2450A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594099 | ||||||
| chrX:139594131
|
G | A | 1 | a0001c0003t0001g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2505+2418C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594131 | ||||||
| chrX:139594229
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2505+2320T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594229 | ||||||
| chrX:139594261
|
C | T | 1 | a0004c0009t0001g0024 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2505+2288G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594261 | ||||||
| chrX:139594295
|
T | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+2254A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594295 | ||||||
| chrX:139594341
|
C | G | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+2208G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594341 | ||||||
| chrX:139594457
|
C | G | 3 | a0001c0001t0001g0173a0001c0005t0001g0152a0001c0005t0001g0154 | 3 | HG02109.hp2 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2505+2092G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594457 | ||||||
| chrX:139594571
|
T | C | 1 | a0001c0003t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2505+1978A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594571 | ||||||
| chrX:139594771
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+1778G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594771 | ||||||
| chrX:139594827
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2505+1722G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594827 | ||||||
| chrX:139594892
|
T | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+1657A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594892 | ||||||
| chrX:139594968
|
A | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237 | 3 | HG00639.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2505+1581T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594968 | ||||||
| chrX:139594972
|
C | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+1577G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139594972 | ||||||
| chrX:139595007
|
C | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2505+1542G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595007 | ||||||
| chrX:139595062
|
A | C | 1 | a0001c0001t0001g0001 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2505+1487T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595062 | ||||||
| chrX:139595078
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2505+1471G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595078 | ||||||
| chrX:139595081
|
G | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+1468C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595081 | ||||||
| chrX:139595125
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2505+1424T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595125 | ||||||
| chrX:139595153
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2505+1396C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595153 | ||||||
| chrX:139595223
|
C | G | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(3): Show | 6 | HG01123.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2505+1326G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595223 | ||||||
| chrX:139595282
|
A | G | 97 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(94): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.2505+1267T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595282 | ||||||
| chrX:139595329
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2505+1220T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595329 | ||||||
| chrX:139595342
|
G | T | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(3): Show | 6 | HG02965.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2505+1207C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595342 | ||||||
| chrX:139595375
|
C | T | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2505+1174G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595375 | ||||||
| chrX:139595441
|
A | G | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2505+1108T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595441 | ||||||
| chrX:139595442
|
T | C | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2505+1107A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595442 | ||||||
| chrX:139595444
|
G | A | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2505+1105C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595444 | ||||||
| chrX:139595449
|
T | C | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2505+1100A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595449 | ||||||
| chrX:139595485
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2505+1064G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595485 | ||||||
| chrX:139595494
|
A | G | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2505+1055T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595494 | ||||||
| chrX:139595498
|
C | G | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2505+1051G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595498 | ||||||
| chrX:139595501
|
C | T | 1 | a0001c0002t0001g0221 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2505+1048G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595501 | ||||||
| chrX:139595517
|
A | T | 1 | a0001c0001t0001g0060 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2505+1032T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595517 | ||||||
| chrX:139595582
|
T | TG | 3 | a0001c0001t0001g0039a0001c0001t0001g0130a0001c0001t0001g0225 | 3 | HG02071.hp1 HG03710.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.2505+966dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595582 | ||||||
| chrX:139595589
|
A | AG | 2 | a0001c0001t0001g0188a0001c0003t0001g0025 | 2 | HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2505+959dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595589 | ||||||
| chrX:139595595
|
G | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+954C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595595 | ||||||
| chrX:139595641
|
T | A | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2505+908A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595641 | ||||||
| chrX:139595658
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+891G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595658 | ||||||
| chrX:139595689
|
G | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+860C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595689 | ||||||
| chrX:139595753
|
TA | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+795delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595753 | ||||||
| chrX:139595909
|
A | G | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(3): Show | 6 | HG02965.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2505+640T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595909 | ||||||
| chrX:139595992
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+557G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595992 | ||||||
| chrX:139596008
|
A | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+541T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139596008 | ||||||
| chrX:139596047
|
T | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+502A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139596047 | ||||||
| chrX:139596049
|
G | A | 9 | a0001c0001t0001g0124a0001c0001t0001g0140a0001c0001t0001g0145others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2505+500C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139596049 | ||||||
| chrX:139596130
|
G | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+419C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139596130 | ||||||
| chrX:139596134
|
T | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0161others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2505+415A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139596134 | ||||||
| chrX:139596187
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2505+362G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139596187 | ||||||
| chrX:139596359
|
A | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.2505+190T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139596359 | ||||||
| chrX:139596791
|
C | G | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2284-21G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139596791 | ||||||
| chrX:139596840
|
AG | A | 1 | a0001c0001t0001g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2284-71delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139596840 | ||||||
| chrX:139596863
|
AC | A | 1 | a0001c0001t0001g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2284-94delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139596863 | ||||||
| chrX:139596926
|
C | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0161others(1): Show | 4 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-156G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139596926 | ||||||
| chrX:139596954
|
TG | T | 1 | a0001c0001t0001g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2284-185delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139596954 | ||||||
| chrX:139596995
|
T | C | 18 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(15): Show | 18 | HG00408.hp1 HG01175.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.2284-225A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139596995 | ||||||
| chrX:139597078
|
C | A | 1 | a0001c0001t0001g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2284-308G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139597078 | ||||||
| chrX:139597322
|
T | G | 2 | a0001c0003t0001g0002a0001c0003t0001g0197 | 3 | HG01346.hp1 HG01433.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2283+138A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139597322 | ||||||
| chrX:139597372
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2283+88G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139597372 | ||||||
| chrX:139597373
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2283+87C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139597373 | ||||||
| chrX:139597422
|
AC | A | 1 | a0001c0001t0001g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2283+37delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139597422 | ||||||
| chrX:139597610
|
T | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2158-25A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 21/28 | chrX | 139597610 | ||||||
| chrX:139597896
|
A | G | 38 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0048others(35): Show | 38 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2158-311T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 21/28 | chrX | 139597896 | ||||||
| chrX:139598121
|
T | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(154): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.2157+285A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 21/28 | chrX | 139598121 | ||||||
| chrX:139598136
|
T | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2157+270A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 21/28 | chrX | 139598136 | ||||||
| chrX:139598346
|
A | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0175a0001c0001t0001g0193others(1): Show | 4 | HG02109.hp1 HG02809.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2157+60T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 21/28 | chrX | 139598346 | ||||||
| chrX:139598601
|
T | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-103A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139598601 | ||||||
| chrX:139598660
|
A | G | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-162T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139598660 | ||||||
| chrX:139598814
|
T | A | 7 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(4): Show | 7 | HG01256.hp1 HG01515.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-316A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139598814 | ||||||
| chrX:139598815
|
A | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(4): Show | 7 | HG01256.hp1 HG01515.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-317T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139598815 | ||||||
| chrX:139598849
|
A | G | 22 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(19): Show | 22 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.2065-351T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139598849 | ||||||
| chrX:139598923
|
A | G | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(3): Show | 6 | HG02965.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2065-425T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139598923 | ||||||
| chrX:139599087
|
A | G | 1 | a0001c0002t0001g0100 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2065-589T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599087 | ||||||
| chrX:139599141
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-643G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599141 | ||||||
| chrX:139599385
|
G | A | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2065-887C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599385 | ||||||
| chrX:139599394
|
CA | C | 1 | a0001c0001t0001g0074 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2065-897delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599394 | ||||||
| chrX:139599409
|
C | T | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(3): Show | 6 | HG02965.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2065-911G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599409 | ||||||
| chrX:139599505
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2065-1007C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599505 | ||||||
| chrX:139599722
|
C | T | 31 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0159others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.2065-1224G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599722 | ||||||
| chrX:139599733
|
CT | C | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2065-1236delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599733 | ||||||
| chrX:139599797
|
T | G | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2065-1299A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599797 | ||||||
| chrX:139600132
|
G | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0142others(7): Show | 10 | HG01261.hp1 HG01496.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2065-1634C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600132 | ||||||
| chrX:139600169
|
GGGGAAAA others(2): Show |
G | 1 | a0001c0002t0001g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2065-1680_2065-167 others(13): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600169 | ||||||
| chrX:139600273
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0175a0001c0001t0001g0193others(1): Show | 4 | HG02109.hp1 HG02809.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-1775G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600273 | ||||||
| chrX:139600407
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2065-1909G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600407 | ||||||
| chrX:139600484
|
A | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064+1922T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600484 | ||||||
| chrX:139600536
|
A | G | 1 | a0001c0002t0001g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2064+1870T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600536 | ||||||
| chrX:139600734
|
A | C | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2064+1672T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600734 | ||||||
| chrX:139600787
|
G | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(3): Show | 6 | HG01123.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2064+1619C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600787 | ||||||
| chrX:139600889
|
C | A | 1 | a0001c0003t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2064+1517G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139600889 | ||||||
| chrX:139601079
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0187 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2064+1327T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601079 | ||||||
| chrX:139601086
|
A | G | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064+1320T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601086 | ||||||
| chrX:139601096
|
T | G | 4 | a0001c0003t0001g0047a0001c0003t0001g0111a0001c0003t0001g0112others(1): Show | 4 | NA18949.hp2 NA18950.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+1310A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601096 | ||||||
| chrX:139601171
|
G | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064+1235C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601171 | ||||||
| chrX:139601232
|
C | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064+1174G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601232 | ||||||
| chrX:139601411
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0161others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2064+995A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601411 | ||||||
| chrX:139601470
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0161others(7): Show | 10 | HG01123.hp2 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2064+936T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601470 | ||||||
| chrX:139601478
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG01891.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2064+928G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601478 | ||||||
| chrX:139601709
|
T | C | 1 | a0001c0003t0001g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2064+697A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601709 | ||||||
| chrX:139601840
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 7 | HG01123.hp2 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064+566A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139601840 | ||||||
| chrX:139602263
|
T | TG | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2064+142dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139602263 | ||||||
| chrX:139602293
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064+113G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139602293 | ||||||
| chrX:139602357
|
G | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064+49C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139602357 | ||||||
| chrX:139602618
|
G | C | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1972-120C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139602618 | ||||||
| chrX:139602914
|
C | T | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1972-416G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139602914 | ||||||
| chrX:139603069
|
C | T | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(26): Show | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.1972-571G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139603069 | ||||||
| chrX:139603353
|
T | A | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(26): Show | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.1972-855A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139603353 | ||||||
| chrX:139603423
|
T | C | 29 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(26): Show | 29 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.1972-925A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139603423 | ||||||
| chrX:139603564
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1972-1066C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139603564 | ||||||
| chrX:139603693
|
G | T | 31 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0159others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1971+988C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139603693 | ||||||
| chrX:139603748
|
T | A | 19 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0135others(16): Show | 19 | HG01243.hp1 HG01261.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1971+933A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139603748 | ||||||
| chrX:139603764
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0107 | 2 | HG01071.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1971+917G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139603764 | ||||||
| chrX:139603856
|
AT | A | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1971+824delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139603856 | ||||||
| chrX:139604054
|
T | C | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1971+627A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604054 | ||||||
| chrX:139604135
|
T | C | 7 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0151others(4): Show | 7 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1971+546A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604135 | ||||||
| chrX:139604310
|
T | A | 9 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0043others(6): Show | 9 | HG00438.hp1 HG01934.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1971+371A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604310 | ||||||
| chrX:139604319
|
C | CA | 72 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0118others(69): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1971+361dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604319 | ||||||
| chrX:139604319
|
C | CAA | 15 | a0001c0001t0001g0022a0001c0002t0001g0015a0001c0002t0001g0057others(12): Show | 15 | HG01109.hp1 HG01123.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1971+360_1971+361d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604319 | ||||||
| chrX:139604562
|
G | A | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(3): Show | 6 | HG02922.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1971+119C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604562 | ||||||
| chrX:139604565
|
C | T | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1971+116G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604565 | ||||||
| chrX:139604579
|
A | G | 2 | a0001c0005t0001g0152a0001c0005t0001g0154 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1971+102T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604579 | ||||||
| chrX:139604815
|
G | C | 1 | a0001c0002t0001g0176 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1901+54C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 18/28 | chrX | 139604815 | ||||||
| chrX:139605156
|
C | CT | 3 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0076 | 3 | HG02273.hp1 HG02293.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1786-173dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 17/28 | chrX | 139605156 | ||||||
| chrX:139605156
|
CT | C | 94 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(91): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1786-173delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 17/28 | chrX | 139605156 | ||||||
| chrX:139605156
|
CTT | C | 8 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1786-174_1786-173d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 17/28 | chrX | 139605156 | ||||||
| chrX:139605268
|
G | T | 1 | a0001c0001t0001g0212 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1786-284C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 17/28 | chrX | 139605268 | ||||||
| chrX:139605461
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1785+252C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 17/28 | chrX | 139605461 | ||||||
| chrX:139605476
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1785+237T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 17/28 | chrX | 139605476 | ||||||
| chrX:139605620
|
C | T | 5 | a0001c0001t0001g0124a0001c0001t0001g0140a0001c0001t0001g0158others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1785+93G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 17/28 | chrX | 139605620 | ||||||
| chrX:139605952
|
T | C | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1719-173A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139605952 | ||||||
| chrX:139606016
|
C | CAT | 61 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0023others(58): Show | 61 | HG00408.hp1 HG00639.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1719-239_1719-238d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139606016 | ||||||
| chrX:139606016
|
C | CATAT | 29 | a0001c0001t0001g0159a0001c0001t0001g0168a0001c0001t0001g0173others(26): Show | 30 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.1719-241_1719-238d others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139606016 | ||||||
| chrX:139606016
|
C | CATATAT | 2 | a0001c0001t0001g0019a0001c0001t0001g0030 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1719-243_1719-238d others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139606016 | ||||||
| chrX:139606381
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1719-602C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139606381 | ||||||
| chrX:139606606
|
G | A | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(3): Show | 6 | HG02922.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1719-827C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139606606 | ||||||
| chrX:139606810
|
TC | T | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1718+880delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139606810 | ||||||
| chrX:139607052
|
T | C | 1 | a0001c0002t0001g0013 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1718+639A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607052 | ||||||
| chrX:139607103
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1718+588G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607103 | ||||||
| chrX:139607150
|
CA | C | 18 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(15): Show | 18 | HG00408.hp1 HG01175.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.1718+540delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607150 | ||||||
| chrX:139607164
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | NA18954.hp1 NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1718+527A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607164 | ||||||
| chrX:139607230
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1718+461A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607230 | ||||||
| chrX:139607253
|
T | C | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1718+438A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607253 | ||||||
| chrX:139607341
|
T | C | 18 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(15): Show | 18 | HG00408.hp1 HG01175.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.1718+350A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607341 | ||||||
| chrX:139607342
|
T | C | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1718+349A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607342 | ||||||
| chrX:139607363
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1718+328G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607363 | ||||||
| chrX:139607419
|
A | C | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(3): Show | 6 | HG01123.hp2 HG01884.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1718+272T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607419 | ||||||
| chrX:139607442
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0040others(1): Show | 4 | HG00735.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1718+249G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607442 | ||||||
| chrX:139607528
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0213 | 2 | NA18991.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1718+163G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607528 | ||||||
| chrX:139607545
|
T | A | 31 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0159others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1718+146A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607545 | ||||||
| chrX:139607907
|
A | AT | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1630-129dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139607907 | ||||||
| chrX:139607932
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237 | 3 | HG00639.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1630-153C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139607932 | ||||||
| chrX:139608001
|
GTA | G | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(3): Show | 6 | HG02922.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1630-224_1630-223d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608001 | ||||||
| chrX:139608013
|
T | C | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-234A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608013 | ||||||
| chrX:139608204
|
CT | C | 7 | a0001c0001t0001g0168a0001c0002t0001g0015a0001c0002t0001g0143others(4): Show | 7 | HG02723.hp2 HG02922.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1630-426delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608204 | ||||||
| chrX:139608532
|
C | T | 2 | a0001c0005t0001g0152a0001c0005t0001g0154 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1630-753G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608532 | ||||||
| chrX:139608602
|
G | T | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(3): Show | 6 | HG02922.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1630-823C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608602 | ||||||
| chrX:139608697
|
A | T | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1630-918T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608697 | ||||||
| chrX:139608901
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0233 | 2 | NA18966.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1630-1122G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608901 | ||||||
| chrX:139608925
|
G | A | 1 | a0001c0001t0002g0202 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1630-1146C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608925 | ||||||
| chrX:139608955
|
C | T | 2 | a0001c0003t0001g0002a0001c0003t0001g0197 | 3 | HG01346.hp1 HG01433.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1630-1176G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608955 | ||||||
| chrX:139608973
|
C | CT | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1630-1195dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139608973 | ||||||
| chrX:139609104
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1629+1197G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139609104 | ||||||
| chrX:139609141
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1629+1160C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139609141 | ||||||
| chrX:139609244
|
G | GA | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1629+1056dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139609244 | ||||||
| chrX:139609279
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1629+1022A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139609279 | ||||||
| chrX:139609291
|
T | C | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1629+1010A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139609291 | ||||||
| chrX:139609548
|
C | CA | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1629+752dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139609548 | ||||||
| chrX:139610064
|
C | T | 1 | a0002c0004t0003g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1629+237G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139610064 | ||||||
| chrX:139610171
|
C | CT | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1629+129dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139610171 | ||||||
| chrX:139610184
|
A | G | 1 | a0002c0004t0003g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1629+117T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139610184 | ||||||
| chrX:139610229
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1629+72C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139610229 | ||||||
| chrX:139610573
|
C | T | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1592-235G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139610573 | ||||||
| chrX:139611255
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1592-917C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139611255 | ||||||
| chrX:139611462
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1592-1124G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139611462 | ||||||
| chrX:139611508
|
G | A | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(3): Show | 6 | HG02922.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1592-1170C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139611508 | ||||||
| chrX:139611651
|
A | G | 6 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(3): Show | 6 | HG02922.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1592-1313T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139611651 | ||||||
| chrX:139611934
|
A | AGT | 2 | a0001c0001t0001g0159a0001c0002t0001g0235 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1591+1280_1591+128 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139611934 | ||||||
| chrX:139611980
|
G | A | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.1591+1236C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139611980 | ||||||
| chrX:139612270
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1591+946C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139612270 | ||||||
| chrX:139612540
|
G | GA | 1 | a0002c0004t0003g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1591+675dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139612540 | ||||||
| chrX:139612540
|
GA | G | 8 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0143others(5): Show | 8 | HG02257.hp2 HG02922.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1591+675delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139612540 | ||||||
| chrX:139612842
|
C | A | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1591+374G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139612842 | ||||||
| chrX:139612957
|
T | C | 2 | a0001c0001t0001g0159a0001c0002t0001g0235 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1591+259A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139612957 | ||||||
| chrX:139613008
|
C | G | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1591+208G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139613008 | ||||||
| chrX:139613149
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237 | 3 | HG00639.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1591+67A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 14/28 | chrX | 139613149 | ||||||
| chrX:139613298
|
A | C | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1544-35T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139613298 | ||||||
| chrX:139613364
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | NA18954.hp1 NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1544-101A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139613364 | ||||||
| chrX:139613564
|
G | A | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1544-301C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139613564 | ||||||
| chrX:139613634
|
C | T | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1544-371G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139613634 | ||||||
| chrX:139613660
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1544-397G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139613660 | ||||||
| chrX:139613735
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1544-472G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139613735 | ||||||
| chrX:139613825
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1544-562T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139613825 | ||||||
| chrX:139614086
|
C | A | 28 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0142others(25): Show | 28 | HG00408.hp1 HG01175.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1543+795G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614086 | ||||||
| chrX:139614116
|
A | C | 1 | a0001c0003t0001g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1543+765T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614116 | ||||||
| chrX:139614380
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1543+501T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614380 | ||||||
| chrX:139614507
|
A | ATG | 10 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG01496.hp1 HG02004.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1543+372_1543+373d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614507 | ||||||
| chrX:139614507
|
A | ATGTG | 1 | a0001c0001t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1543+370_1543+373d others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614507 | ||||||
| chrX:139614507
|
ATG | A | 12 | a0001c0001t0001g0045a0001c0001t0001g0073a0001c0001t0001g0074others(9): Show | 12 | HG01175.hp1 HG02055.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.1543+372_1543+373d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614507 | ||||||
| chrX:139614507
|
ATGTG | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0219 | 2 | NA18952.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1543+370_1543+373d others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614507 | ||||||
| chrX:139614507
|
ATGTGTGT others(1): Show |
A | 9 | a0001c0001t0001g0090a0001c0001t0001g0134a0001c0001t0001g0186others(6): Show | 9 | HG01123.hp2 HG01169.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1543+366_1543+373d others(10): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614507 | ||||||
| chrX:139614507
|
ATGTGTGT others(3): Show |
A | 152 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(149): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1543+364_1543+373d others(12): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614507 | ||||||
| chrX:139614507
|
ATGTGTGT others(7): Show |
A | 2 | a0001c0001t0001g0159a0001c0002t0001g0235 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1543+360_1543+373d others(16): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614507 | ||||||
| chrX:139614790
|
C | T | 37 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0048others(34): Show | 37 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1543+91G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 13/28 | chrX | 139614790 | ||||||
| chrX:139615057
|
G | A | 4 | a0001c0001t0001g0022a0002c0004t0003g0165a0002c0004t0003g0166others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1372-5C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 12/28 | chrX | 139615057 | ||||||
| chrX:139615087
|
A | C | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1372-35T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 12/28 | chrX | 139615087 | ||||||
| chrX:139615164
|
T | C | 37 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0135others(34): Show | 37 | HG00408.hp1 HG01175.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1372-112A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 12/28 | chrX | 139615164 | ||||||
| chrX:139615229
|
CCA | C | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1372-179_1372-178d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 12/28 | chrX | 139615229 | ||||||
| chrX:139615374
|
G | A | 2 | a0001c0002t0001g0221a0001c0002t0001g0222 | 2 | NA18990.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1372-322C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 12/28 | chrX | 139615374 | ||||||
| chrX:139616119
|
G | A | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1371+163C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 12/28 | chrX | 139616119 | ||||||
| chrX:139616493
|
GA | G | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(92): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1180-21delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616493 | ||||||
| chrX:139616493
|
GAA | G | 5 | a0001c0001t0001g0124a0001c0001t0001g0140a0001c0001t0001g0158others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-22_1180-21del others(2): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616493 | ||||||
| chrX:139616506
|
T | C | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(92): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.1180-33A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616506 | ||||||
| chrX:139616597
|
T | TA | 8 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0163others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-125dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616597 | ||||||
| chrX:139616597
|
TA | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0067a0001c0001t0001g0069others(14): Show | 18 | HG01175.hp1 HG02015.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1180-125delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616597 | ||||||
| chrX:139616688
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0030 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1180-215A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616688 | ||||||
| chrX:139616714
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1180-241C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616714 | ||||||
| chrX:139616772
|
C | T | 37 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0135others(34): Show | 37 | HG00408.hp1 HG01175.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1180-299G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616772 | ||||||
| chrX:139616795
|
C | CT | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1180-323dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616795 | ||||||
| chrX:139617009
|
C | T | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1179+504G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139617009 | ||||||
| chrX:139617324
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1179+189G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139617324 | ||||||
| chrX:139617721
|
CA | C | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-18delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139617721 | ||||||
| chrX:139617734
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.988-30T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139617734 | ||||||
| chrX:139617850
|
C | CA | 34 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0074others(31): Show | 35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.988-147dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139617850 | ||||||
| chrX:139617850
|
CA | C | 1 | a0001c0001t0001g0122 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.988-147delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139617850 | ||||||
| chrX:139618131
|
C | G | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-427G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139618131 | ||||||
| chrX:139618257
|
C | T | 92 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.988-553G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139618257 | ||||||
| chrX:139618417
|
C | T | 24 | a0001c0003t0001g0002a0001c0003t0001g0025a0001c0003t0001g0037others(21): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.988-713G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139618417 | ||||||
| chrX:139618506
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.988-802G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139618506 | ||||||
| chrX:139618507
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0162 | 2 | HG01261.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.988-803C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139618507 | ||||||
| chrX:139619036
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0161 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.987+551C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139619036 | ||||||
| chrX:139619386
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 6 | HG02280.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+201G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139619386 | ||||||
| chrX:139619389
|
T | C | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.987+198A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139619389 | ||||||
| chrX:139619566
|
A | T | 1 | a0001c0001t0004g0208 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.987+21T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139619566 | ||||||
| chrX:139619864
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.868-158T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619864 | ||||||
| chrX:139619909
|
G | T | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-203C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619909 | ||||||
| chrX:139619933
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.868-227G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619933 | ||||||
| chrX:139619934
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.868-228C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619934 | ||||||
| chrX:139619997
|
T | TTG | 22 | a0001c0001t0001g0022a0001c0001t0001g0083a0001c0001t0001g0188others(19): Show | 23 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.868-293_868-292dup others(2): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619997 | ||||||
| chrX:139619997
|
T | TTGTG | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0191others(2): Show | 5 | HG01123.hp2 HG01346.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-295_868-292dup others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619997 | ||||||
| chrX:139619997
|
T | TTGTGTGT others(7): Show |
3 | a0001c0003t0001g0062a0001c0003t0001g0138a0001c0003t0001g0246 | 3 | HG00639.hp1 HG01074.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.868-305_868-292dup others(14): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619997 | ||||||
| chrX:139619997
|
TTG | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0194a0001c0001t0001g0237 | 3 | HG00639.hp2 HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.868-293_868-292del others(2): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619997 | ||||||
| chrX:139619997
|
TTGTG | T | 38 | a0001c0001t0001g0023a0001c0001t0001g0124a0001c0001t0001g0129others(35): Show | 38 | HG00408.hp1 HG01175.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.868-295_868-292del others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619997 | ||||||
| chrX:139619997
|
TTGTGTG | T | 2 | a0001c0001t0001g0159a0001c0002t0001g0235 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.868-297_868-292del others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139619997 | ||||||
| chrX:139620025
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0240a0001c0002t0001g0235 | 3 | HG02257.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.868-319C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620025 | ||||||
| chrX:139620025
|
GTGTA | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0168others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.868-323_868-320del others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620025 | ||||||
| chrX:139620027
|
G | A | 48 | a0001c0001t0001g0094a0001c0001t0001g0124a0001c0001t0001g0129others(45): Show | 48 | HG00408.hp1 HG01175.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.868-321C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620027 | ||||||
| chrX:139620027
|
G | GTA | 6 | a0001c0001t0001g0018a0001c0001t0001g0161a0001c0002t0001g0141others(3): Show | 6 | HG01175.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.868-323_868-322dup others(2): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620027 | ||||||
| chrX:139620027
|
G | GTGTA | 1 | a0001c0001t0001g0192 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.868-322_868-321ins others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620027 | ||||||
| chrX:139620027
|
G | GTGTGTGT others(3): Show |
5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-322_868-321ins others(10): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620027 | ||||||
| chrX:139620029
|
A | G | 25 | a0001c0001t0001g0238a0001c0003t0001g0002a0001c0003t0001g0025others(22): Show | 26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.868-323T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620029 | ||||||
| chrX:139620050
|
A | G | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-344T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620050 | ||||||
| chrX:139620163
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.868-457G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620163 | ||||||
| chrX:139620166
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036 | 3 | NA18954.hp1 NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.868-460G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620166 | ||||||
| chrX:139620392
|
C | A | 4 | a0001c0001t0001g0022a0002c0004t0003g0165a0002c0004t0003g0166others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-686G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139620392 | ||||||
| chrX:139621006
|
A | G | 2 | a0001c0005t0001g0152a0001c0005t0001g0154 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.868-1300T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139621006 | ||||||
| chrX:139621045
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.868-1339C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139621045 | ||||||
| chrX:139621547
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.868-1841G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139621547 | ||||||
| chrX:139621685
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.868-1979C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139621685 | ||||||
| chrX:139621758
|
C | T | 2 | a0001c0002t0001g0008a0001c0002t0001g0056 | 2 | NA18941.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.868-2052G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139621758 | ||||||
| chrX:139621844
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.868-2138C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139621844 | ||||||
| chrX:139621924
|
T | C | 28 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0142others(25): Show | 28 | HG00408.hp1 HG01175.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.868-2218A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139621924 | ||||||
| chrX:139622494
|
C | T | 2 | a0001c0001t0001g0159a0001c0002t0001g0235 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.868-2788G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139622494 | ||||||
| chrX:139622647
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.868-2941G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139622647 | ||||||
| chrX:139622719
|
T | C | 15 | a0001c0001t0001g0022a0001c0001t0001g0159a0001c0002t0001g0015others(12): Show | 15 | HG01109.hp1 HG01175.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.868-3013A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139622719 | ||||||
| chrX:139622755
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.868-3049A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139622755 | ||||||
| chrX:139622789
|
A | G | 44 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0048others(41): Show | 44 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.868-3083T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139622789 | ||||||
| chrX:139622892
|
TA | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237 | 3 | HG00639.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.868-3187delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139622892 | ||||||
| chrX:139623116
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237 | 3 | HG00639.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.867+3077C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623116 | ||||||
| chrX:139623398
|
TA | T | 2 | a0001c0005t0001g0152a0001c0005t0001g0154 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.867+2794delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623398 | ||||||
| chrX:139623658
|
C | T | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.867+2535G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623658 | ||||||
| chrX:139623666
|
G | C | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.867+2527C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623666 | ||||||
| chrX:139623667
|
TAA | T | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.867+2524_867+2525d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623667 | ||||||
| chrX:139623672
|
GTATACC | G | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.867+2515_867+2520d others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623672 | ||||||
| chrX:139623682
|
G | C | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.867+2511C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623682 | ||||||
| chrX:139623683
|
T | A | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.867+2510A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623683 | ||||||
| chrX:139623684
|
A | C | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.867+2509T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623684 | ||||||
| chrX:139623739
|
G | T | 2 | a0001c0003t0001g0002a0001c0003t0001g0197 | 3 | HG01346.hp1 HG01433.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.867+2454C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623739 | ||||||
| chrX:139624202
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.867+1991C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139624202 | ||||||
| chrX:139624220
|
A | T | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+1973T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139624220 | ||||||
| chrX:139624443
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.867+1750C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139624443 | ||||||
| chrX:139624531
|
C | CA | 3 | a0001c0001t0001g0107a0001c0002t0001g0006a0001c0002t0001g0057 | 3 | HG01071.hp1 NA18940.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.867+1661dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139624531 | ||||||
| chrX:139624531
|
CA | C | 14 | a0001c0001t0001g0129a0001c0001t0001g0145a0001c0001t0001g0159others(11): Show | 14 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.867+1661delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139624531 | ||||||
| chrX:139625006
|
G | A | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+1187C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625006 | ||||||
| chrX:139625123
|
T | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0175a0001c0001t0001g0193others(1): Show | 4 | HG02109.hp1 HG02809.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+1070A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625123 | ||||||
| chrX:139625242
|
C | T | 2 | a0001c0001t0001g0159a0001c0002t0001g0235 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.867+951G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625242 | ||||||
| chrX:139625527
|
G | A | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.867+666C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625527 | ||||||
| chrX:139625548
|
T | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0094a0001c0001t0001g0161others(7): Show | 10 | HG01123.hp2 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.867+645A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625548 | ||||||
| chrX:139625595
|
T | C | 2 | a0001c0005t0001g0152a0001c0005t0001g0154 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.867+598A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625595 | ||||||
| chrX:139625699
|
T | C | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.867+494A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625699 | ||||||
| chrX:139625929
|
C | T | 7 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0143others(4): Show | 7 | HG02257.hp2 HG02922.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.867+264G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625929 | ||||||
| chrX:139625949
|
G | T | 1 | a0001c0001t0001g0212 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.867+244C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625949 | ||||||
| chrX:139625994
|
C | T | 7 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0143others(4): Show | 7 | HG02257.hp2 HG02922.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.867+199G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625994 | ||||||
| chrX:139625995
|
G | A | 39 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0129others(36): Show | 39 | HG00408.hp1 HG01175.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.867+198C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139625995 | ||||||
| chrX:139626052
|
G | A | 4 | a0001c0003t0001g0047a0001c0003t0001g0111a0001c0003t0001g0112others(1): Show | 4 | NA18949.hp2 NA18950.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+141C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139626052 | ||||||
| chrX:139626176
|
GA | G | 1 | a0001c0001t0001g0195 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.867+16delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139626176 | ||||||
| chrX:139626770
|
C | CA | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.619-15dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139626770 | ||||||
| chrX:139626864
|
T | G | 5 | a0001c0002t0001g0015a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-108A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139626864 | ||||||
| chrX:139626976
|
C | T | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.619-220G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139626976 | ||||||
| chrX:139627556
|
G | A | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-800C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139627556 | ||||||
| chrX:139627660
|
G | A | 10 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007others(7): Show | 10 | HG00408.hp1 NA18941.hp1 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-904C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139627660 | ||||||
| chrX:139627729
|
C | T | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-973G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139627729 | ||||||
| chrX:139627966
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.619-1210T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139627966 | ||||||
| chrX:139628267
|
C | T | 96 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.618+1428G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139628267 | ||||||
| chrX:139628640
|
C | T | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.618+1055G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139628640 | ||||||
| chrX:139628746
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.618+949G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139628746 | ||||||
| chrX:139628866
|
A | C | 2 | a0001c0002t0001g0059a0001c0002t0001g0150 | 2 | NA18973.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.618+829T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139628866 | ||||||
| chrX:139629048
|
C | T | 7 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0143others(4): Show | 7 | HG02257.hp2 HG02922.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+647G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139629048 | ||||||
| chrX:139629049
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.618+646T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139629049 | ||||||
| chrX:139629102
|
A | G | 15 | a0001c0001t0001g0022a0001c0001t0001g0159a0001c0002t0001g0015others(12): Show | 15 | HG01109.hp1 HG01175.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.618+593T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139629102 | ||||||
| chrX:139629141
|
A | C | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.618+554T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139629141 | ||||||
| chrX:139629387
|
C | A | 11 | a0001c0001t0001g0159a0001c0002t0001g0015a0001c0002t0001g0141others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.618+308G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 7/28 | chrX | 139629387 | ||||||
| chrX:139629971
|
T | G | 2 | a0001c0005t0001g0152a0001c0005t0001g0154 | 2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.469-127A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139629971 | ||||||
| chrX:139630106
|
T | G | 1 | a0001c0001t0001g0242 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.469-262A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139630106 | ||||||
| chrX:139630359
|
G | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0168others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-515C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139630359 | ||||||
| chrX:139630368
|
G | GA | 6 | a0001c0001t0001g0145a0001c0001t0001g0173a0001c0001t0001g0175others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-525dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139630368 | ||||||
| chrX:139630450
|
C | T | 5 | a0001c0001t0001g0124a0001c0001t0001g0140a0001c0001t0001g0158others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-606G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139630450 | ||||||
| chrX:139630832
|
T | C | 4 | a0001c0001t0001g0022a0002c0004t0003g0165a0002c0004t0003g0166others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+563A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139630832 | ||||||
| chrX:139631002
|
G | A | 89 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.468+393C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139631002 | ||||||
| chrX:139631059
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0213 | 2 | NA18991.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.468+336A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139631059 | ||||||
| chrX:139631284
|
T | TTTTTG | 36 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0048others(33): Show | 36 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.468+106_468+110dup others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139631284 | ||||||
| chrX:139631304
|
G | GT | 84 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.468+90dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139631304 | ||||||
| chrX:139631516
|
A | G | 11 | a0001c0001t0001g0159a0001c0002t0001g0141a0001c0002t0001g0143others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.352-5T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139631516 | ||||||
| chrX:139631594
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.352-83T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139631594 | ||||||
| chrX:139631746
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.352-235G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139631746 | ||||||
| chrX:139631761
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.352-250G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139631761 | ||||||
| chrX:139631783
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(8): Show | 11 | HG02698.hp1 HG03490.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.352-272T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139631783 | ||||||
| chrX:139631921
|
A | T | 85 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.352-410T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139631921 | ||||||
| chrX:139631960
|
G | T | 4 | a0001c0001t0001g0022a0002c0004t0003g0165a0002c0004t0003g0166others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.351+375C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139631960 | ||||||
| chrX:139631979
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.351+356C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139631979 | ||||||
| chrX:139632222
|
C | CAA | 92 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.351+112_351+113ins others(2): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139632222 | ||||||
| chrX:139632283
|
C | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG01891.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+52G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 5/28 | chrX | 139632283 | ||||||
| chrX:139632505
|
C | T | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-51G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139632505 | ||||||
| chrX:139632618
|
T | C | 11 | a0001c0001t0001g0159a0001c0002t0001g0141a0001c0002t0001g0143others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.232-164A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139632618 | ||||||
| chrX:139632640
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232-186C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139632640 | ||||||
| chrX:139632702
|
T | A | 1 | a0004c0009t0001g0024 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.232-248A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139632702 | ||||||
| chrX:139633131
|
G | C | 1 | a0001c0001t0002g0201 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.232-677C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633131 | ||||||
| chrX:139633211
|
G | A | 2 | a0001c0002t0001g0008a0001c0002t0001g0056 | 2 | NA18941.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.232-757C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633211 | ||||||
| chrX:139633287
|
G | C | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-833C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633287 | ||||||
| chrX:139633316
|
G | C | 4 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-862C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633316 | ||||||
| chrX:139633350
|
G | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0039others(9): Show | 12 | HG00438.hp1 HG01934.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.232-896C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633350 | ||||||
| chrX:139633449
|
T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0161 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.232-995A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633449 | ||||||
| chrX:139633617
|
G | A | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-1163C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633617 | ||||||
| chrX:139633655
|
G | GT | 3 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0003t0001g0112 | 3 | HG02135.hp1 NA18948.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.232-1202dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633655 | ||||||
| chrX:139633920
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.232-1466C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139633920 | ||||||
| chrX:139634122
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.232-1668G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139634122 | ||||||
| chrX:139634224
|
G | A | 81 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.232-1770C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139634224 | ||||||
| chrX:139634227
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.232-1773G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139634227 | ||||||
| chrX:139634240
|
T | C | 1 | a0001c0002t0001g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.232-1786A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139634240 | ||||||
| chrX:139634301
|
G | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0228 | 3 | HG02056.hp1 NA18956.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.232-1847C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139634301 | ||||||
| chrX:139634432
|
T | C | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.232-1978A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139634432 | ||||||
| chrX:139634804
|
G | A | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-2350C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139634804 | ||||||
| chrX:139634969
|
G | A | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.232-2515C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139634969 | ||||||
| chrX:139635042
|
G | C | 81 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.232-2588C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635042 | ||||||
| chrX:139635118
|
A | G | 11 | a0001c0001t0001g0159a0001c0002t0001g0141a0001c0002t0001g0143others(8): Show | 11 | HG01175.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.232-2664T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635118 | ||||||
| chrX:139635156
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.232-2702G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635156 | ||||||
| chrX:139635222
|
G | T | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-2768C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635222 | ||||||
| chrX:139635256
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.232-2802C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635256 | ||||||
| chrX:139635356
|
G | A | 85 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.232-2902C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635356 | ||||||
| chrX:139635543
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.232-3089C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635543 | ||||||
| chrX:139635663
|
AT | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0107 | 2 | HG01071.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.232-3210delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635663 | ||||||
| chrX:139635664
|
T | A | 83 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.232-3210A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635664 | ||||||
| chrX:139635764
|
G | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0187 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.232-3310C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635764 | ||||||
| chrX:139635821
|
T | C | 86 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.232-3367A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635821 | ||||||
| chrX:139635829
|
A | C | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-3375T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635829 | ||||||
| chrX:139635833
|
T | C | 86 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.232-3379A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635833 | ||||||
| chrX:139635851
|
C | A | 1 | a0001c0003t0001g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.232-3397G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635851 | ||||||
| chrX:139635863
|
T | C | 86 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.232-3409A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635863 | ||||||
| chrX:139635895
|
A | ATC | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-3442_232-3441i others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635895 | ||||||
| chrX:139635896
|
C | A | 4 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-3442G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635896 | ||||||
| chrX:139635898
|
C | A | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-3444G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635898 | ||||||
| chrX:139635901
|
G | A | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-3447C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635901 | ||||||
| chrX:139636115
|
A | G | 92 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.232-3661T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636115 | ||||||
| chrX:139636205
|
C | CTAT | 4 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156others(1): Show | 4 | HG03209.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-3754_232-3752d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636205 | ||||||
| chrX:139636249
|
T | G | 86 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.232-3795A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636249 | ||||||
| chrX:139636281
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.232-3827G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636281 | ||||||
| chrX:139636310
|
T | A | 70 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0088others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.232-3856A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636310 | ||||||
| chrX:139636333
|
T | G | 87 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.232-3879A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636333 | ||||||
| chrX:139636348
|
T | C | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232-3894A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636348 | ||||||
| chrX:139636530
|
C | G | 86 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.232-4076G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636530 | ||||||
| chrX:139636599
|
A | T | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232-4145T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636599 | ||||||
| chrX:139636605
|
T | G | 5 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01258.hp1 HG01515.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-4151A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636605 | ||||||
| chrX:139636742
|
C | T | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-4288G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636742 | ||||||
| chrX:139636891
|
G | A | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-4437C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636891 | ||||||
| chrX:139636903
|
G | T | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-4449C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636903 | ||||||
| chrX:139636917
|
C | G | 5 | a0001c0001t0001g0159a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG02257.hp2 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-4463G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636917 | ||||||
| chrX:139636991
|
G | A | 97 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(94): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.232-4537C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636991 | ||||||
| chrX:139637062
|
TG | T | 5 | a0001c0001t0001g0159a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG02257.hp2 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-4609delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637062 | ||||||
| chrX:139637064
|
A | T | 5 | a0001c0001t0001g0159a0001c0002t0001g0143a0001c0002t0001g0155others(2): Show | 5 | HG02257.hp2 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-4610T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637064 | ||||||
| chrX:139637077
|
T | C | 1 | a0001c0003t0001g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.232-4623A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637077 | ||||||
| chrX:139637155
|
T | A | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232-4701A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637155 | ||||||
| chrX:139637168
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.232-4714A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637168 | ||||||
| chrX:139637307
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.232-4853A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637307 | ||||||
| chrX:139637345
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0159a0001c0001t0001g0161others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-4891C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637345 | ||||||
| chrX:139637430
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.232-4976G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637430 | ||||||
| chrX:139637665
|
G | C | 4 | a0001c0001t0001g0022a0002c0004t0003g0165a0002c0004t0003g0166others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-5211C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139637665 | ||||||
| chrX:139638230
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237 | 3 | HG00639.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.232-5776C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638230 | ||||||
| chrX:139638321
|
T | C | 88 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0063others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.232-5867A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638321 | ||||||
| chrX:139638411
|
A | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.232-5957T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638411 | ||||||
| chrX:139638544
|
T | C | 88 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0063others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.232-6090A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638544 | ||||||
| chrX:139638575
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237 | 3 | HG00639.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.232-6121C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638575 | ||||||
| chrX:139638680
|
G | C | 78 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0063others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.232-6226C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638680 | ||||||
| chrX:139638747
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.232-6293G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638747 | ||||||
| chrX:139638836
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237others(1): Show | 4 | HG00639.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-6382C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638836 | ||||||
| chrX:139638838
|
C | T | 9 | a0001c0001t0001g0022a0001c0002t0001g0141a0001c0002t0001g0157others(6): Show | 9 | HG01109.hp1 HG01175.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.232-6384G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638838 | ||||||
| chrX:139638963
|
T | C | 88 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0063others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.232-6509A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638963 | ||||||
| chrX:139639128
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+6440A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639128 | ||||||
| chrX:139639137
|
A | G | 88 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0063others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.231+6431T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639137 | ||||||
| chrX:139639201
|
A | G | 84 | a0001c0001t0001g0018a0001c0001t0001g0063a0001c0001t0001g0065others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.231+6367T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639201 | ||||||
| chrX:139639287
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+6281T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639287 | ||||||
| chrX:139639306
|
A | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0168others(2): Show | 5 | HG02109.hp2 HG02723.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+6262T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639306 | ||||||
| chrX:139639346
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.231+6222A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639346 | ||||||
| chrX:139639371
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.231+6197T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639371 | ||||||
| chrX:139639501
|
G | T | 84 | a0001c0001t0001g0018a0001c0001t0001g0063a0001c0001t0001g0065others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.231+6067C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639501 | ||||||
| chrX:139639641
|
A | T | 1 | a0001c0002t0001g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.231+5927T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639641 | ||||||
| chrX:139639676
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0184a0001c0001t0001g0237 | 3 | HG00639.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.231+5892G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639676 | ||||||
| chrX:139639948
|
ATAT | A | 70 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0088others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.231+5617_231+5619d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639948 | ||||||
| chrX:139639964
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0168others(3): Show | 6 | HG02109.hp2 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+5604G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639964 | ||||||
| chrX:139640026
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0066others(4): Show | 7 | HG01928.hp1 HG02129.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+5542G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640026 | ||||||
| chrX:139640039
|
GCGGTAGT others(9): Show |
G | 1 | a0001c0003t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.231+5513_231+5528d others(18): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640039 | ||||||
| chrX:139640041
|
G | A | 25 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0088others(22): Show | 25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.231+5527C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640041 | ||||||
| chrX:139640068
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.231+5500C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640068 | ||||||
| chrX:139640151
|
C | T | 11 | a0001c0001t0001g0124a0001c0001t0001g0140a0001c0001t0001g0145others(8): Show | 11 | HG01243.hp1 HG02109.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.231+5417G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640151 | ||||||
| chrX:139640270
|
T | G | 1 | a0001c0002t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.231+5298A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640270 | ||||||
| chrX:139640689
|
T | A | 86 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0063others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.231+4879A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640689 | ||||||
| chrX:139640723
|
TGGTCAAG others(22): Show |
T | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+4816_231+4844d others(31): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640723 | ||||||
| chrX:139640755
|
T | C | 1 | a0001c0003t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.231+4813A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640755 | ||||||
| chrX:139640844
|
G | GA | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+4723dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640844 | ||||||
| chrX:139640877
|
T | C | 78 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0063others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.231+4691A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640877 | ||||||
| chrX:139640886
|
C | T | 5 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(2): Show | 5 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+4682G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640886 | ||||||
| chrX:139640976
|
C | T | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(2): Show | 5 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.231+4592G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640976 | ||||||
| chrX:139641167
|
A | AAT | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.231+4399_231+4400d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641167 | ||||||
| chrX:139641167
|
AAT | A | 1 | a0001c0003t0001g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.231+4399_231+4400d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641167 | ||||||
| chrX:139641170
|
A | ATG | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+4397_231+4398i others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641170 | ||||||
| chrX:139641515
|
T | TC | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+4052dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641515 | ||||||
| chrX:139641544
|
A | AT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+4023dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641544 | ||||||
| chrX:139641562
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+4006T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641562 | ||||||
| chrX:139641569
|
C | G | 1 | a0001c0003t0001g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.231+3999G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641569 | ||||||
| chrX:139641570
|
C | CT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+3997dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641570 | ||||||
| chrX:139641669
|
AAG | A | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.231+3897_231+3898d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641669 | ||||||
| chrX:139641786
|
T | C | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+3782A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641786 | ||||||
| chrX:139642110
|
A | AG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+3457_231+3458i others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642110 | ||||||
| chrX:139642499
|
C | CG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+3068dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642499 | ||||||
| chrX:139642566
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.231+3002C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642566 | ||||||
| chrX:139642627
|
CA | C | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2940delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642627 | ||||||
| chrX:139642682
|
G | GA | 3 | a0001c0001t0001g0018a0001c0001t0001g0158a0001c0001t0001g0217 | 3 | HG02145.hp1 HG03098.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.231+2885dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642682 | ||||||
| chrX:139642682
|
GA | G | 14 | a0001c0001t0001g0094a0001c0001t0001g0187a0001c0001t0001g0229others(11): Show | 14 | HG00621.hp1 HG00639.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.231+2885delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642682 | ||||||
| chrX:139642759
|
A | G | 9 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0066others(6): Show | 9 | HG00741.hp2 HG01928.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.231+2809T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642759 | ||||||
| chrX:139642770
|
C | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0173a0001c0001t0001g0175others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.231+2798G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642770 | ||||||
| chrX:139642821
|
CA | C | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2746delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642821 | ||||||
| chrX:139642827
|
G | GA | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2740dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642827 | ||||||
| chrX:139642831
|
AG | A | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2736delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642831 | ||||||
| chrX:139642859
|
G | GA | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.231+2708dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139642859 | ||||||
| chrX:139643025
|
G | GT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2542dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643025 | ||||||
| chrX:139643070
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.231+2498T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643070 | ||||||
| chrX:139643109
|
G | GA | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2458dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643109 | ||||||
| chrX:139643116
|
T | TA | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2451dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643116 | ||||||
| chrX:139643140
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.231+2428C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643140 | ||||||
| chrX:139643253
|
A | G | 1 | a0001c0002t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.231+2315T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643253 | ||||||
| chrX:139643301
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(80): Show | 84 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.231+2267A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643301 | ||||||
| chrX:139643313
|
C | CA | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2254dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643313 | ||||||
| chrX:139643329
|
A | AC | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2238dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643329 | ||||||
| chrX:139643343
|
T | TG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2224dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643343 | ||||||
| chrX:139643348
|
G | GC | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2219_231+2220i others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643348 | ||||||
| chrX:139643390
|
G | GA | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2177dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643390 | ||||||
| chrX:139643417
|
T | C | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2151A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643417 | ||||||
| chrX:139643440
|
G | GT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2127dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643440 | ||||||
| chrX:139643623
|
A | AAGG | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+1944_231+1945i others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643623 | ||||||
| chrX:139643624
|
G | C | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+1944C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643624 | ||||||
| chrX:139643842
|
A | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0187 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.231+1726T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643842 | ||||||
| chrX:139643911
|
G | GT | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+1656dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643911 | ||||||
| chrX:139643929
|
GA | G | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+1638delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643929 | ||||||
| chrX:139643946
|
T | TA | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+1621dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643946 | ||||||
| chrX:139643993
|
CA | C | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+1574delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643993 | ||||||
| chrX:139644052
|
G | A | 90 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.231+1516C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644052 | ||||||
| chrX:139644168
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.231+1400C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644168 | ||||||
| chrX:139644178
|
A | G | 4 | a0001c0003t0001g0047a0001c0003t0001g0111a0001c0003t0001g0112others(1): Show | 4 | NA18949.hp2 NA18950.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+1390T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644178 | ||||||
| chrX:139644433
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.231+1135A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644433 | ||||||
| chrX:139644451
|
AT | A | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+1116delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644451 | ||||||
| chrX:139644549
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.231+1019G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644549 | ||||||
| chrX:139644596
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.231+972A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644596 | ||||||
| chrX:139644751
|
T | A | 4 | a0001c0002t0001g0141a0001c0002t0001g0157a0001c0002t0001g0160others(1): Show | 4 | HG01175.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+817A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644751 | ||||||
| chrX:139645000
|
C | T | 1 | a0002c0004t0003g0189 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.231+568G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139645000 | ||||||
| chrX:139645309
|
C | T | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(92): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.231+259G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139645309 | ||||||
| chrX:139645375
|
T | C | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.231+193A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139645375 | ||||||
| chrX:139645801
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.141-143A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 3/28 | chrX | 139645801 | ||||||
| chrX:139645802
|
C | T | 5 | a0001c0003t0001g0037a0001c0003t0001g0051a0001c0003t0001g0064others(2): Show | 5 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-144G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 3/28 | chrX | 139645802 | ||||||
| chrX:139645987
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(76): Show | 80 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.141-329T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 3/28 | chrX | 139645987 | ||||||
| chrX:139646060
|
T | C | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.141-402A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 3/28 | chrX | 139646060 | ||||||
| chrX:139646287
|
CTTT | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(69): Show | 73 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.140+499_140+501del others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 3/28 | chrX | 139646287 | ||||||
| chrX:139646311
|
G | C | 35 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0063others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.140+478C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 3/28 | chrX | 139646311 | ||||||
| chrX:139647066
|
GT | G | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.26-164delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647066 | ||||||
| chrX:139647333
|
A | G | 1 | a0001c0002t0001g0059 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.26-430T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647333 | ||||||
| chrX:139647336
|
C | T | 26 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0079others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.26-433G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647336 | ||||||
| chrX:139647584
|
G | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0237a0001c0005t0001g0152others(1): Show | 4 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-681C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647584 | ||||||
| chrX:139647721
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01123.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.26-818G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647721 | ||||||
| chrX:139647742
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.26-839C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647742 | ||||||
| chrX:139647792
|
T | C | 3 | a0001c0001t0002g0101a0001c0001t0002g0199a0001c0001t0002g0202 | 3 | NA18995.hp1 NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.26-889A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647792 | ||||||
| chrX:139647925
|
A | T | 1 | a0001c0002t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.26-1022T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647925 | ||||||
| chrX:139647972
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-1069G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139647972 | ||||||
| chrX:139648137
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.26-1234G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139648137 | ||||||
| chrX:139648377
|
G | GC | 2 | a0001c0001t0001g0129a0002c0004t0003g0189 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.26-1475dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139648377 | ||||||
| chrX:139648385
|
C | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0107 | 2 | HG01071.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.26-1482G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139648385 | ||||||
| chrX:139648424
|
C | T | 95 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(92): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.26-1521G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139648424 | ||||||
| chrX:139648486
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26-1583C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139648486 | ||||||
| chrX:139648627
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26-1724C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139648627 | ||||||
| chrX:139649634
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.25+2086G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649634 | ||||||
| chrX:139649645
|
CT | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.25+2074delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649645 | ||||||
| chrX:139649649
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.25+2071T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649649 | ||||||
| chrX:139649819
|
C | G | 64 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.25+1901G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649819 | ||||||
| chrX:139649903
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+1817G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649903 | ||||||
| chrX:139649925
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.25+1795A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649925 | ||||||
| chrX:139650085
|
CG | C | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.25+1634delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650085 | ||||||
| chrX:139650130
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0237others(7): Show | 10 | HG00639.hp2 HG01109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.25+1590C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650130 | ||||||
| chrX:139650196
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0219 | 2 | NA18952.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.25+1524T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650196 | ||||||
| chrX:139650215
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.25+1505C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650215 | ||||||
| chrX:139650457
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.25+1263G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650457 | ||||||
| chrX:139650467
|
G | T | 1 | a0001c0002t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+1253C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650467 | ||||||
| chrX:139650513
|
T | TCTCAATA | 67 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.25+1206_25+1207ins others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650513 | ||||||
| chrX:139650513
|
T | TCTGAATA | 36 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0072others(33): Show | 37 | HG01175.hp2 HG01261.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.25+1206_25+1207ins others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650513 | ||||||
| chrX:139650535
|
T | A | 36 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0072others(33): Show | 37 | HG01175.hp2 HG01261.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.25+1185A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650535 | ||||||
| chrX:139650605
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.25+1115A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650605 | ||||||
| chrX:139650708
|
C | A | 30 | a0001c0001t0001g0072a0001c0001t0001g0142a0001c0001t0001g0144others(27): Show | 31 | HG01261.hp1 HG01346.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.25+1012G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650708 | ||||||
| chrX:139650945
|
T | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(89): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.25+775A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650945 | ||||||
| chrX:139650978
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0168others(9): Show | 13 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.25+742A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139650978 | ||||||
| chrX:139651008
|
C | T | 29 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0030others(26): Show | 29 | HG00639.hp2 HG00741.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.25+712G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651008 | ||||||
| chrX:139651016
|
AG | A | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.25+703delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651016 | ||||||
| chrX:139651095
|
C | T | 32 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0063others(29): Show | 33 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(30): Show |
intron_variant | MODIFIER | c.25+625G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651095 | ||||||
| chrX:139651122
|
CACAAAAA others(24): Show |
C | 25 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0124others(22): Show | 26 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.25+567_25+597delTC others(29): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651122 | ||||||
| chrX:139651124
|
CA | C | 1 | a0001c0003t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+595delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651124 | ||||||
| chrX:139651137
|
G | A | 71 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0018others(68): Show | 72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.25+583C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651137 | ||||||
| chrX:139651144
|
ATGCCGCT others(35): Show |
A | 1 | a0001c0003t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+534_25+575delAC others(40): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651144 | ||||||
| chrX:139651190
|
A | T | 1 | a0001c0003t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+530T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651190 | ||||||
| chrX:139651197
|
ATTTAT | A | 1 | a0001c0003t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+518_25+522delAT others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651197 | ||||||
| chrX:139651305
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.25+415C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651305 | ||||||
| chrX:139651439
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.25+281A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651439 | ||||||
| chrX:139651506
|
C | T | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+214G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651506 | ||||||
| chrX:139651629
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.25+91A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651629 | ||||||
| chrX:139651639
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.25+81C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651639 | ||||||
| chrX:139651689
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(53): Show | 59 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.25+31T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651689 | ||||||
| chrX:139651805
|
T | C | 5 | a0001c0001t0001g0019a0001c0002t0001g0151a0001c0005t0001g0152others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-17A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139651805 | ||||||
| chrX:139651965
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-177C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139651965 | ||||||
| chrX:139652077
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0169 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-289G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652077 | ||||||
| chrX:139652105
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-317A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652105 | ||||||
| chrX:139652150
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01123.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-44-362G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652150 | ||||||
| chrX:139652271
|
A | G | 8 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0168others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-483T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652271 | ||||||
| chrX:139652341
|
C | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-553G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652341 | ||||||
| chrX:139652390
|
T | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(60): Show | 66 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.-44-602A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652390 | ||||||
| chrX:139652448
|
C | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-660G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652448 | ||||||
| chrX:139652688
|
G | C | 1 | a0001c0002t0001g0221 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-44-900C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652688 | ||||||
| chrX:139652736
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(85): Show | 91 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.-44-948C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652736 | ||||||
| chrX:139652878
|
T | TAA | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-1092_-44-1091d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652878 | ||||||
| chrX:139652939
|
A | AC | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-44-1152dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652939 | ||||||
| chrX:139652940
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-1152G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652940 | ||||||
| chrX:139652946
|
C | T | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-1158G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652946 | ||||||
| chrX:139652947
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-1159C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652947 | ||||||
| chrX:139652979
|
T | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-1191A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139652979 | ||||||
| chrX:139653006
|
C | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-1218G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653006 | ||||||
| chrX:139653015
|
A | T | 1 | a0001c0001t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-44-1227T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653015 | ||||||
| chrX:139653104
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-1316C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653104 | ||||||
| chrX:139653147
|
A | C | 3 | a0001c0003t0001g0061a0001c0003t0001g0062a0001c0003t0001g0138 | 3 | HG00639.hp1 HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-44-1359T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653147 | ||||||
| chrX:139653306
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44-1518A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653306 | ||||||
| chrX:139653413
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(68): Show | 74 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.-44-1625C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653413 | ||||||
| chrX:139653548
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(72): Show | 78 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-44-1760A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653548 | ||||||
| chrX:139653566
|
C | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44-1778G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653566 | ||||||
| chrX:139653781
|
TC | T | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-44-1994delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653781 | ||||||
| chrX:139653836
|
T | A | 1 | a0001c0001t0001g0001 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-44-2048A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653836 | ||||||
| chrX:139653856
|
A | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-2068T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653856 | ||||||
| chrX:139653888
|
A | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44-2100T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653888 | ||||||
| chrX:139654059
|
A | G | 19 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44-2271T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654059 | ||||||
| chrX:139654087
|
T | C | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-2299A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654087 | ||||||
| chrX:139654206
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-44-2418C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654206 | ||||||
| chrX:139654284
|
C | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44-2496G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654284 | ||||||
| chrX:139654345
|
G | A | 58 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0040others(55): Show | 58 | HG00280.hp1 HG00438.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-44-2557C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654345 | ||||||
| chrX:139654397
|
T | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44-2609A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654397 | ||||||
| chrX:139654463
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-2675G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654463 | ||||||
| chrX:139654542
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(50): Show | 56 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.-44-2754T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654542 | ||||||
| chrX:139654565
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-44-2777A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654565 | ||||||
| chrX:139654721
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-44-2933G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654721 | ||||||
| chrX:139654833
|
T | C | 10 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0168others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44-3045A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654833 | ||||||
| chrX:139654843
|
G | A | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-3055C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139654843 | ||||||
| chrX:139655173
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-3385A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655173 | ||||||
| chrX:139655229
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-44-3441A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655229 | ||||||
| chrX:139655232
|
A | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-3444T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655232 | ||||||
| chrX:139655301
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-44-3513G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655301 | ||||||
| chrX:139655476
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-44-3688G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655476 | ||||||
| chrX:139655477
|
G | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-3689C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655477 | ||||||
| chrX:139655516
|
G | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-3728C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655516 | ||||||
| chrX:139655522
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-44-3734A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655522 | ||||||
| chrX:139655540
|
C | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44-3752G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655540 | ||||||
| chrX:139655569
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0169 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-3781C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655569 | ||||||
| chrX:139655646
|
T | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-3858A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655646 | ||||||
| chrX:139655671
|
TC | T | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-44-3884delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655671 | ||||||
| chrX:139655693
|
G | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-3905C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139655693 | ||||||
| chrX:139656003
|
C | T | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-4215G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656003 | ||||||
| chrX:139656040
|
G | GT | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-44-4253dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656040 | ||||||
| chrX:139656040
|
GT | G | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-44-4253delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656040 | ||||||
| chrX:139656154
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44-4366G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656154 | ||||||
| chrX:139656319
|
C | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(59): Show | 65 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.-44-4531G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656319 | ||||||
| chrX:139656320
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44-4532G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656320 | ||||||
| chrX:139656342
|
G | A | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-4554C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656342 | ||||||
| chrX:139656709
|
T | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0052others(22): Show | 28 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-44-4921A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656709 | ||||||
| chrX:139656761
|
C | T | 1 | a0001c0002t0001g0059 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-44-4973G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656761 | ||||||
| chrX:139656854
|
T | TA | 1 | a0001c0001t0001g0215 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-44-5067dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656854 | ||||||
| chrX:139656916
|
G | GAT | 2 | a0001c0001t0001g0142a0001c0001t0001g0162 | 2 | HG01261.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-44-5130_-44-5129d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656916 | ||||||
| chrX:139657261
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-5473G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139657261 | ||||||
| chrX:139657287
|
G | T | 2 | a0001c0001t0001g0095a0001c0002t0001g0093 | 2 | NA19003.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-44-5499C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139657287 | ||||||
| chrX:139657288
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-44-5500A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139657288 | ||||||
| chrX:139657293
|
G | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-5505C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139657293 | ||||||
| chrX:139657355
|
G | C | 7 | a0001c0001t0001g0129a0001c0001t0001g0168a0001c0001t0001g0173others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-5567C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139657355 | ||||||
| chrX:139657746
|
C | G | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 26 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-44-5958G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139657746 | ||||||
| chrX:139657953
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0052others(22): Show | 28 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-44-6165C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139657953 | ||||||
| chrX:139658049
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-6261A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658049 | ||||||
| chrX:139658082
|
C | CA | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(6): Show | 9 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44-6295dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658082 | ||||||
| chrX:139658266
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-6478A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658266 | ||||||
| chrX:139658307
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44-6519G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658307 | ||||||
| chrX:139658340
|
GT | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(81): Show | 87 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.-44-6553delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658340 | ||||||
| chrX:139658654
|
T | TA | 1 | a0001c0001t0001g0092 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-44-6867dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658654 | ||||||
| chrX:139658667
|
G | GT | 41 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0029others(38): Show | 41 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-44-6880dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658667 | ||||||
| chrX:139658667
|
G | GTT | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-44-6881_-44-6880d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658667 | ||||||
| chrX:139658667
|
G | GTTT | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-44-6882_-44-6880d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658667 | ||||||
| chrX:139658667
|
G | GTTTTTTT | 4 | a0001c0001t0001g0021a0001c0001t0001g0187a0001c0002t0001g0141others(1): Show | 4 | HG02486.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44-6886_-44-6880d others(9): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658667 | ||||||
| chrX:139658667
|
G | GTTTTTTT others(1): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0140others(4): Show | 7 | HG02451.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-6887_-44-6880d others(10): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658667 | ||||||
| chrX:139658667
|
G | GTTTTTTT others(2): Show |
1 | a0001c0001t0001g0179 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-44-6888_-44-6880d others(11): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658667 | ||||||
| chrX:139658667
|
GT | G | 12 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0084others(9): Show | 12 | HG01255.hp1 HG01346.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-6880delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658667 | ||||||
| chrX:139658667
|
GTT | G | 8 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0168others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-6881_-44-6880d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658667 | ||||||
| chrX:139658729
|
C | T | 3 | a0001c0001t0001g0168a0002c0004t0003g0165a0002c0004t0003g0166 | 3 | HG01884.hp1 HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-44-6941G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658729 | ||||||
| chrX:139658820
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-44-7032G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658820 | ||||||
| chrX:139658870
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-7082C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658870 | ||||||
| chrX:139658904
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-7116C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658904 | ||||||
| chrX:139659025
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-44-7237G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139659025 | ||||||
| chrX:139659280
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0161 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-44-7492G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139659280 | ||||||
| chrX:139659312
|
TA | T | 2 | a0001c0001t0001g0039a0001c0002t0001g0157 | 2 | HG06807.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-44-7525delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139659312 | ||||||
| chrX:139659322
|
A | T | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44-7534T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139659322 | ||||||
| chrX:139659342
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44-7554A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139659342 | ||||||
| chrX:139659617
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0007g0068 | 3 | HG02055.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-44-7829A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139659617 | ||||||
| chrX:139659636
|
G | A | 13 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(10): Show | 13 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44-7848C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139659636 | ||||||
| chrX:139659702
|
C | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0148others(13): Show | 16 | HG00673.hp1 HG02132.hp1 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.-44-7914G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139659702 | ||||||
| chrX:139660033
|
A | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-8245T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139660033 | ||||||
| chrX:139660249
|
A | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-8461T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139660249 | ||||||
| chrX:139660284
|
T | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-8496A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139660284 | ||||||
| chrX:139660313
|
A | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-8525T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139660313 | ||||||
| chrX:139660478
|
T | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-8690A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139660478 | ||||||
| chrX:139660546
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44-8758A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139660546 | ||||||
| chrX:139660554
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-44-8766A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139660554 | ||||||
| chrX:139660807
|
G | T | 1 | a0003c0007t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-44-9019C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139660807 | ||||||
| chrX:139661108
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-44-9320A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139661108 | ||||||
| chrX:139661393
|
C | T | 1 | a0001c0003t0001g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-44-9605G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139661393 | ||||||
| chrX:139661515
|
C | T | 1 | a0001c0001t0005g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-44-9727G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139661515 | ||||||
| chrX:139661625
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-9837A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139661625 | ||||||
| chrX:139662064
|
G | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0133a0001c0001t0001g0134others(5): Show | 8 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-10276C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662064 | ||||||
| chrX:139662307
|
A | ACCCCTAT others(304): Show |
1 | a0001c0002t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-44-10520_-44-1051 others(315): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662307 | ||||||
| chrX:139662307
|
A | ACCCCTAT others(305): Show |
2 | a0001c0002t0001g0143a0001c0002t0001g0156 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-44-10520_-44-1051 others(316): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662307 | ||||||
| chrX:139662307
|
A | ACCCCTAT others(305): Show |
9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-10520_-44-1051 others(316): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662307 | ||||||
| chrX:139662594
|
T | TG | 1 | a0001c0002t0001g0222 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-44-10807dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662594 | ||||||
| chrX:139662597
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-44-10809C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662597 | ||||||
| chrX:139662936
|
G | GA | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-44-11149dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662936 | ||||||
| chrX:139662944
|
G | GT | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-44-11157dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662944 | ||||||
| chrX:139662951
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-11163G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662951 | ||||||
| chrX:139662969
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-44-11181G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662969 | ||||||
| chrX:139663193
|
AT | A | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-44-11406delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663193 | ||||||
| chrX:139663393
|
TGTAA | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-11609_-44-1160 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663393 | ||||||
| chrX:139663504
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-11716C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663504 | ||||||
| chrX:139663568
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-44-11780A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663568 | ||||||
| chrX:139663576
|
G | GT | 19 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01109.hp1 HG01256.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-44-11789dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663576 | ||||||
| chrX:139663576
|
G | GTT | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0163others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44-11790_-44-1178 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663576 | ||||||
| chrX:139663576
|
GT | G | 1 | a0001c0001t0001g0180 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-44-11789delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663576 | ||||||
| chrX:139663577
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-44-11789A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663577 | ||||||
| chrX:139663817
|
T | C | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-12029A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663817 | ||||||
| chrX:139663833
|
G | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-44-12045C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663833 | ||||||
| chrX:139663884
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-44-12096T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663884 | ||||||
| chrX:139663998
|
G | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-12210C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139663998 | ||||||
| chrX:139664037
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-44-12249G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664037 | ||||||
| chrX:139664065
|
T | C | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-12277A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664065 | ||||||
| chrX:139664161
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-12373A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664161 | ||||||
| chrX:139664184
|
T | G | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-12396A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664184 | ||||||
| chrX:139664295
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-12507G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664295 | ||||||
| chrX:139664320
|
C | CA | 12 | a0001c0001t0001g0016a0001c0001t0001g0054a0001c0001t0001g0121others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-12533dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664320 | ||||||
| chrX:139664320
|
C | CAA | 11 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 11 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44-12534_-44-1253 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664320 | ||||||
| chrX:139664320
|
CA | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0219a0001c0002t0001g0093others(1): Show | 4 | HG00735.hp2 NA19003.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44-12533delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664320 | ||||||
| chrX:139664321
|
A | AAAC | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-12534_-44-1253 others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664321 | ||||||
| chrX:139664325
|
A | AAC | 1 | a0001c0002t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-44-12538_-44-1253 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664325 | ||||||
| chrX:139664328
|
A | AAC | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-12541_-44-1254 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664328 | ||||||
| chrX:139664331
|
A | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0006t0001g0223others(1): Show | 4 | HG02071.hp1 HG02083.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-12543T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664331 | ||||||
| chrX:139664395
|
T | C | 11 | a0001c0001t0001g0129a0001c0001t0001g0163a0001c0001t0001g0164others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44-12607A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139664395 | ||||||
| chrX:139665546
|
G | A | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-13758C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665546 | ||||||
| chrX:139665691
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-44-13903T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665691 | ||||||
| chrX:139665814
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-44-14026C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665814 | ||||||
| chrX:139665897
|
G | GTA | 13 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0070others(10): Show | 13 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44-14111_-44-1411 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665897 | ||||||
| chrX:139665897
|
G | GTATA | 14 | a0001c0001t0001g0014a0001c0001t0001g0063a0001c0001t0001g0088others(11): Show | 14 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44-14113_-44-1411 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665897 | ||||||
| chrX:139665897
|
G | GTATATA | 2 | a0001c0001t0001g0118a0001c0003t0001g0116 | 2 | HG00738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-44-14115_-44-1411 others(10): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665897 | ||||||
| chrX:139665897
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44-14119_-44-1411 others(14): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665897 | ||||||
| chrX:139665897
|
GTA | G | 9 | a0001c0001t0001g0029a0001c0001t0001g0109a0001c0001t0001g0120others(6): Show | 9 | HG02647.hp1 HG02723.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44-14111_-44-1411 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665897 | ||||||
| chrX:139665897
|
GTATA | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0231 | 2 | HG02004.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-44-14113_-44-1411 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665897 | ||||||
| chrX:139665897
|
GTATATA | G | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-44-14115_-44-1411 others(10): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665897 | ||||||
| chrX:139665899
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(52): Show | 57 | HG00621.hp1 HG00735.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.-44-14111T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665899 | ||||||
| chrX:139665899
|
AT | A | 1 | a0001c0001t0001g0084 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-44-14112delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665899 | ||||||
| chrX:139665901
|
A | G | 33 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 33 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44-14113T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665901 | ||||||
| chrX:139665903
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-14115T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665903 | ||||||
| chrX:139665913
|
AT | A | 1 | a0001c0002t0001g0100 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-44-14126delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665913 | ||||||
| chrX:139665916
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-44-14140_-44-1412 others(16): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665916 | ||||||
| chrX:139665918
|
TATATATA others(3): Show |
T | 9 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0177others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-14140_-44-1413 others(14): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665918 | ||||||
| chrX:139665920
|
TATATATA others(1): Show |
T | 22 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0129others(19): Show | 22 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.-44-14140_-44-1413 others(12): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665920 | ||||||
| chrX:139665922
|
TATATAC | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0186 | 2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-44-14140_-44-1413 others(10): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665922 | ||||||
| chrX:139665924
|
TATAC | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0147 | 3 | HG01167.hp1 HG01169.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-44-14140_-44-1413 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665924 | ||||||
| chrX:139665926
|
T | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0010t0001g0125 | 3 | HG01069.hp1 HG01071.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-44-14138A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665926 | ||||||
| chrX:139665926
|
TAC | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0052others(33): Show | 38 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-44-14140_-44-1413 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665926 | ||||||
| chrX:139665928
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 12 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-14140G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665928 | ||||||
| chrX:139665962
|
T | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-14174A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665962 | ||||||
| chrX:139665990
|
TACAC | T | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-14206_-44-1420 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139665990 | ||||||
| chrX:139666163
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(47): Show | 53 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.-44-14375A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666163 | ||||||
| chrX:139666209
|
C | CT | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0090others(10): Show | 13 | HG01169.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44-14422dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666209 | ||||||
| chrX:139666209
|
CT | C | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(2): Show | 5 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-14422delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666209 | ||||||
| chrX:139666267
|
TC | T | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-44-14480delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666267 | ||||||
| chrX:139666468
|
T | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-14680A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666468 | ||||||
| chrX:139666471
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0245a0001c0001t0002g0101 | 3 | HG02027.hp1 NA18747.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-44-14683A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666471 | ||||||
| chrX:139666499
|
AT | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-44-14712delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666499 | ||||||
| chrX:139666531
|
TC | T | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-44-14744delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666531 | ||||||
| chrX:139666575
|
T | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-14787A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666575 | ||||||
| chrX:139666594
|
CT | C | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-44-14807delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666594 | ||||||
| chrX:139666851
|
G | GT | 1 | a0001c0001t0001g0232 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-44-15064dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666851 | ||||||
| chrX:139666886
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-44-15098T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139666886 | ||||||
| chrX:139667196
|
C | CT | 25 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0044others(22): Show | 25 | HG01069.hp1 HG01071.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.-44-15409dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667196 | ||||||
| chrX:139667196
|
C | CTT | 2 | a0001c0001t0001g0232a0001c0002t0001g0222 | 2 | NA19063.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-44-15410_-44-1540 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667196 | ||||||
| chrX:139667196
|
CT | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(63): Show | 69 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.-44-15409delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667196 | ||||||
| chrX:139667196
|
CTT | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(17): Show | 20 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-44-15410_-44-1540 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667196 | ||||||
| chrX:139667196
|
CTTT | C | 1 | a0001c0001t0001g0134 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-44-15411_-44-1540 others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667196 | ||||||
| chrX:139667250
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-44-15462C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667250 | ||||||
| chrX:139667331
|
C | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-15543G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667331 | ||||||
| chrX:139667367
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-44-15579G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667367 | ||||||
| chrX:139667408
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0126 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-44-15620C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667408 | ||||||
| chrX:139667557
|
C | T | 1 | a0001c0002t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44-15769G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667557 | ||||||
| chrX:139667563
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-44-15775C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667563 | ||||||
| chrX:139667691
|
T | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0006t0001g0223others(1): Show | 4 | HG02071.hp1 HG02083.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-15903A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667691 | ||||||
| chrX:139667699
|
A | AG | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-44-15912dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667699 | ||||||
| chrX:139667828
|
G | A | 1 | a0001c0003t0001g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-44-16040C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667828 | ||||||
| chrX:139667870
|
T | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0063a0001c0001t0001g0088others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-16082A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667870 | ||||||
| chrX:139667873
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0007g0068 | 3 | HG02055.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-44-16085A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667873 | ||||||
| chrX:139667908
|
T | C | 1 | a0001c0002t0001g0198 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-44-16120A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667908 | ||||||
| chrX:139668021
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-44-16233G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668021 | ||||||
| chrX:139668099
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-44-16311G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668099 | ||||||
| chrX:139668141
|
G | A | 1 | a0001c0003t0001g0185 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-44-16353C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668141 | ||||||
| chrX:139668268
|
A | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-16480T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668268 | ||||||
| chrX:139668275
|
T | TC | 1 | a0001c0002t0001g0006 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-44-16488dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668275 | ||||||
| chrX:139668284
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-44-16496G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668284 | ||||||
| chrX:139668304
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(50): Show | 56 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.-44-16516A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668304 | ||||||
| chrX:139668416
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(46): Show | 52 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.-44-16628C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668416 | ||||||
| chrX:139668518
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(86): Show | 92 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.-44-16730T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668518 | ||||||
| chrX:139668603
|
C | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-16815G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668603 | ||||||
| chrX:139668740
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-44-16952G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668740 | ||||||
| chrX:139668767
|
C | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0002t0001g0235 | 3 | HG02922.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-44-16979G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668767 | ||||||
| chrX:139668847
|
A | AG | 1 | a0001c0002t0001g0006 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-44-17060dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668847 | ||||||
| chrX:139668859
|
T | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0072a0001c0001t0001g0227others(8): Show | 11 | HG00673.hp1 NA18940.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44-17071A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668859 | ||||||
| chrX:139668900
|
G | GT | 1 | a0001c0002t0001g0006 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-44-17113dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668900 | ||||||
| chrX:139668913
|
CA | C | 1 | a0001c0002t0001g0006 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-44-17126delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668913 | ||||||
| chrX:139669050
|
CA | C | 1 | a0001c0002t0001g0006 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-44-17263delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669050 | ||||||
| chrX:139669101
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-17313C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669101 | ||||||
| chrX:139669120
|
AT | A | 1 | a0001c0002t0001g0006 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-44-17333delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669120 | ||||||
| chrX:139669131
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0162 | 2 | HG01261.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-44-17343C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669131 | ||||||
| chrX:139669351
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-44-17563C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669351 | ||||||
| chrX:139669634
|
G | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-17846C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669634 | ||||||
| chrX:139669761
|
G | GA | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-44-17974dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669761 | ||||||
| chrX:139669891
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0230 | 2 | NA18950.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-44-18103C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669891 | ||||||
| chrX:139669996
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-44-18208G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139669996 | ||||||
| chrX:139670135
|
T | TTTTTC | 33 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 33 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44-18352_-44-1834 others(9): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139670135 | ||||||
| chrX:139670189
|
G | GA | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-18402dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139670189 | ||||||
| chrX:139670242
|
AG | A | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-44-18455delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139670242 | ||||||
| chrX:139670389
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-18601A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139670389 | ||||||
| chrX:139670545
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(48): Show | 54 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.-44-18757C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139670545 | ||||||
| chrX:139670920
|
C | G | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-19132G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139670920 | ||||||
| chrX:139670971
|
T | C | 3 | a0001c0001t0001g0231a0001c0001t0001g0234a0001c0001t0001g0242 | 3 | HG00408.hp2 NA18943.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-44-19183A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139670971 | ||||||
| chrX:139671153
|
T | C | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-19365A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671153 | ||||||
| chrX:139671213
|
G | A | 26 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(23): Show | 26 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-44-19425C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671213 | ||||||
| chrX:139671325
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-19537A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671325 | ||||||
| chrX:139671382
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-19594G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671382 | ||||||
| chrX:139671469
|
C | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0002t0001g0235 | 3 | HG02922.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-44-19681G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671469 | ||||||
| chrX:139671539
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-19751A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671539 | ||||||
| chrX:139671577
|
T | TCC | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-19791_-44-1979 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671577 | ||||||
| chrX:139671582
|
A | G | 10 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0168others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44-19794T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671582 | ||||||
| chrX:139671584
|
T | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-19796A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671584 | ||||||
| chrX:139671585
|
T | G | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-19797A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671585 | ||||||
| chrX:139671947
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-20159G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139671947 | ||||||
| chrX:139672022
|
G | T | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-20234C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672022 | ||||||
| chrX:139672023
|
A | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(83): Show | 89 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.-44-20235T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672023 | ||||||
| chrX:139672083
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-20295T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672083 | ||||||
| chrX:139672110
|
CTGTT | C | 1 | a0001c0001t0001g0107 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-44-20326_-44-2032 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672110 | ||||||
| chrX:139672123
|
C | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-44-20335G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672123 | ||||||
| chrX:139672172
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-44-20384T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672172 | ||||||
| chrX:139672308
|
C | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-20520G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672308 | ||||||
| chrX:139672427
|
T | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0220 | 2 | NA19077.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-44-20639A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672427 | ||||||
| chrX:139672484
|
A | G | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 36 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.-44-20696T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672484 | ||||||
| chrX:139672562
|
A | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-20774T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672562 | ||||||
| chrX:139672569
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-44-20781A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672569 | ||||||
| chrX:139672852
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0130 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-44-21064G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672852 | ||||||
| chrX:139672920
|
A | G | 17 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0129others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-44-21132T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139672920 | ||||||
| chrX:139673022
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-44-21234C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673022 | ||||||
| chrX:139673100
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-44-21312G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673100 | ||||||
| chrX:139673101
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-21313C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673101 | ||||||
| chrX:139673124
|
T | G | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-21336A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673124 | ||||||
| chrX:139673151
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-44-21363G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673151 | ||||||
| chrX:139673152
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-44-21364C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673152 | ||||||
| chrX:139673200
|
C | T | 1 | a0001c0005t0001g0152 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-44-21412G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673200 | ||||||
| chrX:139673281
|
AT | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-44-21494delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673281 | ||||||
| chrX:139673294
|
G | GT | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-44-21507dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673294 | ||||||
| chrX:139673354
|
C | T | 10 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0168others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44-21566G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673354 | ||||||
| chrX:139673439
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-44-21651A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673439 | ||||||
| chrX:139673488
|
T | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-44-21700A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673488 | ||||||
| chrX:139673642
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-44-21854T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673642 | ||||||
| chrX:139673783
|
G | T | 1 | a0001c0003t0001g0111 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-44-21995C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139673783 | ||||||
| chrX:139674144
|
C | CTT | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 36 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.-44-22358_-44-2235 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674144 | ||||||
| chrX:139674225
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-44-22437C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674225 | ||||||
| chrX:139674279
|
T | C | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 36 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.-44-22491A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674279 | ||||||
| chrX:139674358
|
G | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-22570C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674358 | ||||||
| chrX:139674362
|
T | C | 1 | a0001c0003t0001g0246 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-44-22574A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674362 | ||||||
| chrX:139674388
|
C | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-22600G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674388 | ||||||
| chrX:139674485
|
G | A | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-22697C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674485 | ||||||
| chrX:139674611
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-44-22823C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674611 | ||||||
| chrX:139674806
|
G | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-23018C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139674806 | ||||||
| chrX:139675050
|
C | T | 1 | a0001c0001t0004g0208 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-44-23262G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675050 | ||||||
| chrX:139675138
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-44-23350C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675138 | ||||||
| chrX:139675190
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-23402G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675190 | ||||||
| chrX:139675216
|
G | GT | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 36 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.-44-23429dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675216 | ||||||
| chrX:139675291
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-23503G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675291 | ||||||
| chrX:139675460
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-44-23672C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675460 | ||||||
| chrX:139675475
|
A | C | 35 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-44-23687T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675475 | ||||||
| chrX:139675480
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-23692C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675480 | ||||||
| chrX:139675514
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-23726G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675514 | ||||||
| chrX:139675634
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-23846G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675634 | ||||||
| chrX:139675715
|
G | GCCTGTAT others(15): Show |
1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-23949_-44-2392 others(26): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675715 | ||||||
| chrX:139675729
|
T | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0158a0001c0002t0001g0157others(3): Show | 6 | HG01175.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-23941A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675729 | ||||||
| chrX:139675795
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44-24007T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675795 | ||||||
| chrX:139675912
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-24124A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139675912 | ||||||
| chrX:139676031
|
C | T | 1 | a0001c0002t0001g0005 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-44-24243G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676031 | ||||||
| chrX:139676035
|
C | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-24247G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676035 | ||||||
| chrX:139676222
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-44-24434C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676222 | ||||||
| chrX:139676230
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-44-24442G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676230 | ||||||
| chrX:139676250
|
AG | A | 1 | a0001c0001t0001g0227 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-44-24463delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676250 | ||||||
| chrX:139676670
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44-24882T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676670 | ||||||
| chrX:139676700
|
C | T | 30 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-44-24912G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676700 | ||||||
| chrX:139676732
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-24944A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676732 | ||||||
| chrX:139676836
|
C | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-25048G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676836 | ||||||
| chrX:139676970
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-25182G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676970 | ||||||
| chrX:139677272
|
T | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(12): Show | 15 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44-25484A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139677272 | ||||||
| chrX:139677417
|
C | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-25629G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139677417 | ||||||
| chrX:139677639
|
TC | T | 1 | a0001c0001t0001g0227 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-44-25852delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139677639 | ||||||
| chrX:139677958
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-44-26170A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139677958 | ||||||
| chrX:139677976
|
G | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0168others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44-26188C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139677976 | ||||||
| chrX:139678044
|
TC | T | 1 | a0001c0001t0001g0227 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-44-26257delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678044 | ||||||
| chrX:139678082
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-44-26294C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678082 | ||||||
| chrX:139678085
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-44-26297G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678085 | ||||||
| chrX:139678130
|
T | C | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-26342A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678130 | ||||||
| chrX:139678172
|
T | A | 1 | a0001c0002t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44-26384A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678172 | ||||||
| chrX:139678706
|
A | G | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-44-26918T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678706 | ||||||
| chrX:139678803
|
A | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-44-27015T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678803 | ||||||
| chrX:139678846
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-44-27058G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678846 | ||||||
| chrX:139678900
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-27112G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139678900 | ||||||
| chrX:139679473
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-44-27685A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139679473 | ||||||
| chrX:139679557
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-44-27769A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139679557 | ||||||
| chrX:139679746
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-44-27958C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139679746 | ||||||
| chrX:139679782
|
T | C | 1 | a0001c0002t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44-27994A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139679782 | ||||||
| chrX:139679799
|
A | C | 59 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(56): Show | 59 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(56): Show |
intron_variant | MODIFIER | c.-44-28011T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139679799 | ||||||
| chrX:139680038
|
A | G | 1 | a0001c0003t0001g0037 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-45+28068T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139680038 | ||||||
| chrX:139680114
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-45+27992A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139680114 | ||||||
| chrX:139680262
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0227 | 2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-45+27844A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139680262 | ||||||
| chrX:139680312
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-45+27794A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139680312 | ||||||
| chrX:139680512
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-45+27594G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139680512 | ||||||
| chrX:139680518
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+27588C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139680518 | ||||||
| chrX:139680604
|
C | T | 30 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-45+27502G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139680604 | ||||||
| chrX:139680868
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0123 | 3 | NA18960.hp1 NA18984.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-45+27238A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139680868 | ||||||
| chrX:139681218
|
A | C | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+26888T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139681218 | ||||||
| chrX:139681441
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-45+26665C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139681441 | ||||||
| chrX:139681595
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-45+26511A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139681595 | ||||||
| chrX:139681637
|
T | C | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45+26469A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139681637 | ||||||
| chrX:139681673
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0110 | 2 | HG01099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-45+26433A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139681673 | ||||||
| chrX:139681839
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0169a0001c0002t0001g0141 | 3 | HG02970.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-45+26267C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139681839 | ||||||
| chrX:139682038
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-45+26068T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682038 | ||||||
| chrX:139682107
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0052others(22): Show | 28 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-45+25999G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682107 | ||||||
| chrX:139682181
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(49): Show | 55 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.-45+25925A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682181 | ||||||
| chrX:139682576
|
C | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+25530G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682576 | ||||||
| chrX:139682789
|
G | A | 2 | a0001c0003t0001g0111a0001c0003t0001g0112 | 2 | NA18950.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-45+25317C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682789 | ||||||
| chrX:139682836
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-45+25270G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682836 | ||||||
| chrX:139682936
|
T | TC | 1 | a0001c0003t0001g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-45+25169dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682936 | ||||||
| chrX:139682990
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+25116G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682990 | ||||||
| chrX:139683356
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0002t0001g0151others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+24750A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139683356 | ||||||
| chrX:139683724
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-45+24382C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139683724 | ||||||
| chrX:139683802
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0052others(22): Show | 28 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-45+24304C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139683802 | ||||||
| chrX:139683889
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01123.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-45+24217A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139683889 | ||||||
| chrX:139683961
|
A | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0002t0001g0235 | 3 | HG02922.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-45+24145T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139683961 | ||||||
| chrX:139684031
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+24075G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139684031 | ||||||
| chrX:139684049
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+24057T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139684049 | ||||||
| chrX:139684260
|
A | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+23846T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139684260 | ||||||
| chrX:139684379
|
G | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+23727C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139684379 | ||||||
| chrX:139684409
|
A | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG00438.hp2 HG02004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+23697T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139684409 | ||||||
| chrX:139684426
|
C | T | 3 | a0001c0002t0001g0196a0001c0003t0001g0002a0001c0003t0001g0197 | 4 | HG01346.hp1 HG01433.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+23680G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139684426 | ||||||
| chrX:139684949
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+23157A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139684949 | ||||||
| chrX:139685005
|
TA | T | 1 | a0001c0002t0001g0222 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-45+23100delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685005 | ||||||
| chrX:139685164
|
C | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0161 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-45+22942G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685164 | ||||||
| chrX:139685204
|
A | T | 1 | a0001c0002t0001g0057 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-45+22902T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685204 | ||||||
| chrX:139685346
|
C | T | 6 | a0001c0001t0001g0124a0001c0001t0001g0158a0001c0002t0001g0157others(3): Show | 6 | HG01175.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+22760G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685346 | ||||||
| chrX:139685347
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0140others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-45+22759C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685347 | ||||||
| chrX:139685527
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45+22579G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685527 | ||||||
| chrX:139685564
|
C | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0052a0001c0001t0001g0053others(15): Show | 20 | HG00621.hp1 HG00735.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.-45+22542G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685564 | ||||||
| chrX:139685564
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45+22542G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685564 | ||||||
| chrX:139685926
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-45+22180A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685926 | ||||||
| chrX:139685938
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0079 | 3 | HG01192.hp1 HG01928.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-45+22168C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139685938 | ||||||
| chrX:139686017
|
T | TA | 1 | a0001c0003t0001g0114 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-45+22088dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686017 | ||||||
| chrX:139686031
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45+22075G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686031 | ||||||
| chrX:139686061
|
C | T | 2 | a0001c0001t0001g0215a0001c0002t0001g0222 | 2 | NA19009.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-45+22045G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686061 | ||||||
| chrX:139686070
|
TA | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(34): Show | 37 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.-45+22035delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686070 | ||||||
| chrX:139686070
|
TAA | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.-45+22034_-45+2203 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686070 | ||||||
| chrX:139686070
|
TAAA | T | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-45+22033_-45+2203 others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686070 | ||||||
| chrX:139686083
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-45+22023T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686083 | ||||||
| chrX:139686113
|
C | T | 2 | a0001c0001t0001g0140a0001c0002t0001g0141 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-45+21993G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686113 | ||||||
| chrX:139686343
|
C | T | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45+21763G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686343 | ||||||
| chrX:139686358
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-45+21748A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686358 | ||||||
| chrX:139686523
|
G | GA | 9 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 9 | HG02015.hp1 HG02040.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45+21582dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686523 | ||||||
| chrX:139686523
|
GA | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0081others(5): Show | 8 | HG02056.hp1 NA18956.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.-45+21582delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686523 | ||||||
| chrX:139686583
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-45+21523C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686583 | ||||||
| chrX:139686793
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-45+21313C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686793 | ||||||
| chrX:139687063
|
T | TAC | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-45+21041_-45+2104 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139687063 | ||||||
| chrX:139687063
|
T | TACAC | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-45+21039_-45+2104 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139687063 | ||||||
| chrX:139687191
|
A | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-45+20915T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139687191 | ||||||
| chrX:139687401
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0002t0001g0235 | 3 | HG02922.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-45+20705C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139687401 | ||||||
| chrX:139687445
|
A | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+20661T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139687445 | ||||||
| chrX:139687738
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-45+20368C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139687738 | ||||||
| chrX:139687850
|
T | A | 30 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0129others(27): Show | 30 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.-45+20256A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139687850 | ||||||
| chrX:139687919
|
C | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0188 | 2 | HG03831.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-45+20187G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139687919 | ||||||
| chrX:139688180
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0162 | 2 | HG01261.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-45+19926T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688180 | ||||||
| chrX:139688199
|
A | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-45+19907T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688199 | ||||||
| chrX:139688297
|
G | A | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45+19809C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688297 | ||||||
| chrX:139688422
|
C | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.-45+19684G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688422 | ||||||
| chrX:139688426
|
G | A | 2 | a0001c0001t0001g0118a0001c0003t0001g0137 | 2 | HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.-45+19680C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688426 | ||||||
| chrX:139688606
|
G | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.-45+19500C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688606 | ||||||
| chrX:139688642
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0001g0145others(4): Show | 8 | HG01243.hp1 HG01496.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-45+19464G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688642 | ||||||
| chrX:139688663
|
G | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(65): Show | 71 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.-45+19443C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688663 | ||||||
| chrX:139688791
|
T | C | 169 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.-45+19315A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688791 | ||||||
| chrX:139688797
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+19309T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688797 | ||||||
| chrX:139688863
|
G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0052others(22): Show | 28 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-45+19243C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688863 | ||||||
| chrX:139688901
|
AC | A | 1 | a0001c0002t0001g0222 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-45+19204delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688901 | ||||||
| chrX:139688909
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0177a0001c0001t0001g0179others(2): Show | 5 | HG02451.hp1 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+19197C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688909 | ||||||
| chrX:139688926
|
AT | A | 1 | a0001c0002t0001g0222 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-45+19179delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139688926 | ||||||
| chrX:139689058
|
TC | T | 1 | a0001c0002t0001g0222 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-45+19047delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139689058 | ||||||
| chrX:139689302
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-45+18804A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139689302 | ||||||
| chrX:139689581
|
C | T | 1 | a0001c0003t0001g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-45+18525G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139689581 | ||||||
| chrX:139689643
|
T | TTTGCATA others(120): Show |
1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+18462_-45+1846 others(131): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139689643 | ||||||
| chrX:139689697
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-45+18409G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139689697 | ||||||
| chrX:139689815
|
CT | C | 1 | a0001c0002t0001g0222 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-45+18290delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139689815 | ||||||
| chrX:139689991
|
C | A | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0175others(3): Show | 6 | HG01243.hp1 HG01496.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+18115G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139689991 | ||||||
| chrX:139690157
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-45+17949G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690157 | ||||||
| chrX:139690218
|
C | CA | 67 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(64): Show | 70 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.-45+17887dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690218 | ||||||
| chrX:139690229
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-45+17877A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690229 | ||||||
| chrX:139690338
|
G | GT | 46 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(43): Show | 49 | HG00621.hp1 HG00735.hp1 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.-45+17767dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690338 | ||||||
| chrX:139690338
|
G | GTT | 136 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.-45+17766_-45+1776 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690338 | ||||||
| chrX:139690338
|
G | GTTT | 31 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(28): Show | 31 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-45+17765_-45+1776 others(7): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690338 | ||||||
| chrX:139690338
|
G | GTTTT | 15 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0043others(12): Show | 15 | HG00438.hp2 HG02004.hp1 HG02273.hp2 others(12): Show |
intron_variant | MODIFIER | c.-45+17764_-45+1776 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690338 | ||||||
| chrX:139690338
|
G | GTTTTT | 7 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0001g0045others(4): Show | 7 | HG01109.hp1 NA18949.hp1 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+17763_-45+1776 others(9): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690338 | ||||||
| chrX:139690344
|
T | TG | 6 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0002t0001g0015others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+17761_-45+1776 others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690344 | ||||||
| chrX:139690425
|
C | G | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+17681G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690425 | ||||||
| chrX:139690614
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+17492G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690614 | ||||||
| chrX:139691122
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0213 | 2 | NA18991.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-45+16984T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691122 | ||||||
| chrX:139691345
|
T | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-45+16761A>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691345 | ||||||
| chrX:139691497
|
C | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(48): Show | 54 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.-45+16609G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691497 | ||||||
| chrX:139691552
|
C | T | 123 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.-45+16554G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691552 | ||||||
| chrX:139691602
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-45+16504A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691602 | ||||||
| chrX:139691722
|
AGT | A | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-45+16382_-45+1638 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691722 | ||||||
| chrX:139691730
|
T | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | NA18952.hp1 NA18954.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+16376A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691730 | ||||||
| chrX:139691736
|
C | CG | 1 | a0001c0001t0001g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-45+16369dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691736 | ||||||
| chrX:139692050
|
C | T | 241 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-45+16056G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139692050 | ||||||
| chrX:139692220
|
C | T | 4 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG02015.hp1 HG02135.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+15886G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139692220 | ||||||
| chrX:139692385
|
C | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01192.hp1 HG01928.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-45+15721G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139692385 | ||||||
| chrX:139692578
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-45+15528C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139692578 | ||||||
| chrX:139692791
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+15315G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139692791 | ||||||
| chrX:139692881
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-45+15225A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139692881 | ||||||
| chrX:139692959
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-45+15147C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139692959 | ||||||
| chrX:139693023
|
C | T | 2 | a0001c0003t0001g0037a0001c0003t0001g0051 | 2 | HG00099.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-45+15083G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693023 | ||||||
| chrX:139693428
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-45+14678T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693428 | ||||||
| chrX:139693483
|
A | AAC | 2 | a0001c0001t0001g0063a0001c0001t0001g0186 | 2 | HG01099.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-45+14621_-45+1462 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693483 | ||||||
| chrX:139693483
|
AAC | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-45+14621_-45+1462 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693483 | ||||||
| chrX:139693483
|
AACAC | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0017others(58): Show | 64 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-45+14619_-45+1462 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693483 | ||||||
| chrX:139693582
|
A | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-45+14524T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693582 | ||||||
| chrX:139693796
|
A | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-45+14310T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693796 | ||||||
| chrX:139693932
|
TA | T | 1 | a0001c0001t0001g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-45+14173delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693932 | ||||||
| chrX:139693971
|
T | TTA | 1 | a0001c0001t0001g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-45+14134_-45+1413 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139693971 | ||||||
| chrX:139694128
|
G | GGA | 1 | a0001c0001t0001g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-45+13977_-45+1397 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139694128 | ||||||
| chrX:139694383
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-45+13723G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139694383 | ||||||
| chrX:139694393
|
CA | C | 1 | a0001c0001t0001g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-45+13712delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139694393 | ||||||
| chrX:139694405
|
G | GA | 5 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG01934.hp1 HG02615.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+13700dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139694405 | ||||||
| chrX:139694405
|
GA | G | 1 | a0001c0002t0001g0013 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-45+13700delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139694405 | ||||||
| chrX:139694953
|
A | G | 1 | a0001c0003t0001g0246 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-45+13153T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139694953 | ||||||
| chrX:139694956
|
T | C | 1 | a0001c0002t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-45+13150A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139694956 | ||||||
| chrX:139695032
|
C | CT | 26 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0058others(23): Show | 26 | HG00673.hp1 HG01261.hp1 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.-45+13073dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139695032 | ||||||
| chrX:139695032
|
C | CTT | 1 | a0001c0001t0001g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-45+13072_-45+1307 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139695032 | ||||||
| chrX:139695032
|
CT | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0052others(25): Show | 31 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-45+13073delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139695032 | ||||||
| chrX:139695221
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-45+12885C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139695221 | ||||||
| chrX:139695409
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-45+12697C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139695409 | ||||||
| chrX:139696210
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-45+11896A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696210 | ||||||
| chrX:139696230
|
CAG | C | 1 | a0001c0001t0001g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-45+11874_-45+1187 others(6): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696230 | ||||||
| chrX:139696280
|
CCCTT | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0052a0001c0001t0001g0053others(15): Show | 20 | HG00621.hp1 HG00735.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.-45+11822_-45+1182 others(8): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696280 | ||||||
| chrX:139696334
|
T | TC | 1 | a0001c0010t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-45+11771_-45+1177 others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696334 | ||||||
| chrX:139696334
|
T | TTTCTC | 147 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-45+11767_-45+1177 others(9): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696334 | ||||||
| chrX:139696341
|
T | TCTCTTCT others(3): Show |
27 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0036others(24): Show | 27 | HG00673.hp1 HG02071.hp1 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.-45+11764_-45+1176 others(14): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696341 | ||||||
| chrX:139696341
|
T | TCTCTTCT others(8): Show |
2 | a0001c0002t0001g0059a0001c0002t0001g0150 | 2 | NA18973.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-45+11764_-45+1176 others(19): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696341 | ||||||
| chrX:139696341
|
TCTCTC | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(15): Show | 18 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-45+11760_-45+1176 others(9): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696341 | ||||||
| chrX:139696341
|
TCTCTCCT others(3): Show |
T | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(3): Show | 6 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+11755_-45+1176 others(14): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696341 | ||||||
| chrX:139696341
|
TCTCTCCT others(13): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-45+11745_-45+1176 others(24): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696341 | ||||||
| chrX:139696346
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0022others(39): Show | 45 | HG00280.hp1 HG00621.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-45+11760G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696346 | ||||||
| chrX:139696351
|
C | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-45+11755G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696351 | ||||||
| chrX:139696356
|
C | T | 5 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(2): Show | 5 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+11750G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696356 | ||||||
| chrX:139696476
|
C | T | 1 | a0001c0003t0001g0061 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-45+11630G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696476 | ||||||
| chrX:139696485
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-45+11621C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696485 | ||||||
| chrX:139696516
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-45+11590G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696516 | ||||||
| chrX:139696526
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-45+11580G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696526 | ||||||
| chrX:139696598
|
AT | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0177others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+11507delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696598 | ||||||
| chrX:139696952
|
T | TA | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+11153dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696952 | ||||||
| chrX:139697394
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-45+10712T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139697394 | ||||||
| chrX:139697420
|
A | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0177a0001c0001t0001g0179others(2): Show | 5 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+10686T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139697420 | ||||||
| chrX:139697468
|
T | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-45+10638A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139697468 | ||||||
| chrX:139697780
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-45+10326T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139697780 | ||||||
| chrX:139697815
|
C | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0191others(2): Show | 5 | HG00639.hp2 HG01123.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+10291G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139697815 | ||||||
| chrX:139697820
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-45+10286C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139697820 | ||||||
| chrX:139697985
|
C | CA | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+10120dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139697985 | ||||||
| chrX:139697997
|
G | C | 3 | a0001c0002t0001g0143a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG03453.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45+10109C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139697997 | ||||||
| chrX:139698001
|
G | A | 156 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-45+10105C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698001 | ||||||
| chrX:139698096
|
GC | G | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+10009delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698096 | ||||||
| chrX:139698155
|
A | AAAAATAA others(9): Show |
1 | a0001c0003t0001g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-45+9950_-45+9951i others(18): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698155 | ||||||
| chrX:139698208
|
A | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0171others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+9898T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698208 | ||||||
| chrX:139698519
|
G | T | 1 | a0001c0003t0001g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-45+9587C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698519 | ||||||
| chrX:139698691
|
A | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0044others(25): Show | 28 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-45+9415T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698691 | ||||||
| chrX:139698822
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+9284T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698822 | ||||||
| chrX:139698864
|
A | C | 1 | a0001c0002t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-45+9242T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698864 | ||||||
| chrX:139698956
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-45+9150T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139698956 | ||||||
| chrX:139699507
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-45+8599C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699507 | ||||||
| chrX:139699524
|
GC | G | 1 | a0001c0002t0001g0013 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-45+8581delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699524 | ||||||
| chrX:139699586
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-45+8520C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699586 | ||||||
| chrX:139699607
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+8499C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699607 | ||||||
| chrX:139699711
|
A | AT | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+8394dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699711 | ||||||
| chrX:139699738
|
AT | A | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+8367delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699738 | ||||||
| chrX:139699802
|
TA | T | 1 | a0001c0002t0001g0013 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-45+8303delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699802 | ||||||
| chrX:139699817
|
A | AT | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+8288dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699817 | ||||||
| chrX:139699983
|
G | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0177others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+8123C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699983 | ||||||
| chrX:139700030
|
G | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-45+8076C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700030 | ||||||
| chrX:139700135
|
GT | G | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+7970delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700135 | ||||||
| chrX:139700235
|
GT | G | 1 | a0001c0002t0001g0013 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-45+7870delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700235 | ||||||
| chrX:139700315
|
AT | A | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+7790delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700315 | ||||||
| chrX:139700352
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-45+7754C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700352 | ||||||
| chrX:139700409
|
G | GA | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7696_-45+7697i others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700409 | ||||||
| chrX:139700428
|
T | TA | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7677_-45+7678i others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700428 | ||||||
| chrX:139700486
|
A | AC | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7619dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700486 | ||||||
| chrX:139700543
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-45+7563G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700543 | ||||||
| chrX:139700604
|
C | CT | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7501dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700604 | ||||||
| chrX:139700752
|
G | GT | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7353dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700752 | ||||||
| chrX:139700758
|
A | AT | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7347_-45+7348i others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700758 | ||||||
| chrX:139700837
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-45+7269G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700837 | ||||||
| chrX:139700851
|
G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 26 | HG00621.hp1 HG01243.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.-45+7255C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700851 | ||||||
| chrX:139700882
|
T | TG | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7223dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700882 | ||||||
| chrX:139700904
|
A | AT | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7201dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700904 | ||||||
| chrX:139700988
|
G | GA | 1 | a0001c0001t0001g0233 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-45+7117dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700988 | ||||||
| chrX:139701032
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-45+7074G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701032 | ||||||
| chrX:139701065
|
AG | A | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+7040delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701065 | ||||||
| chrX:139701083
|
AG | A | 1 | a0001c0002t0001g0013 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-45+7022delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701083 | ||||||
| chrX:139701087
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-45+7019C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701087 | ||||||
| chrX:139701155
|
CT | C | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6950delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701155 | ||||||
| chrX:139701254
|
GA | G | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6851delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701254 | ||||||
| chrX:139701275
|
CA | C | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6830delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701275 | ||||||
| chrX:139701361
|
G | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG01167.hp1 HG01169.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-45+6745C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701361 | ||||||
| chrX:139701485
|
AAT | A | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6619_-45+6620d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701485 | ||||||
| chrX:139701490
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6616G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701490 | ||||||
| chrX:139701651
|
A | AC | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6454dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701651 | ||||||
| chrX:139701670
|
CT | C | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6435delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701670 | ||||||
| chrX:139701745
|
TA | T | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6360delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701745 | ||||||
| chrX:139701759
|
T | TAC | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6345_-45+6346d others(4): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701759 | ||||||
| chrX:139701807
|
A | AT | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6298dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701807 | ||||||
| chrX:139701947
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-45+6159C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701947 | ||||||
| chrX:139702001
|
T | TC | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6104dupG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702001 | ||||||
| chrX:139702113
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-45+5993A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702113 | ||||||
| chrX:139702177
|
C | CA | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5928dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702177 | ||||||
| chrX:139702203
|
AT | A | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5902delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702203 | ||||||
| chrX:139702261
|
AC | A | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5844delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702261 | ||||||
| chrX:139702428
|
T | TA | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5677dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702428 | ||||||
| chrX:139702606
|
G | GT | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5499_-45+5500i others(3): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702606 | ||||||
| chrX:139702608
|
A | T | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5498T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702608 | ||||||
| chrX:139702659
|
GA | G | 1 | a0001c0001t0001g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5446delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702659 | ||||||
| chrX:139702679
|
TA | T | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+5426delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702679 | ||||||
| chrX:139702875
|
C | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0168others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+5231G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702875 | ||||||
| chrX:139703205
|
C | G | 2 | a0001c0001t0001g0140a0001c0002t0001g0141 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-45+4901G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139703205 | ||||||
| chrX:139703280
|
G | C | 1 | a0001c0003t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-45+4826C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139703280 | ||||||
| chrX:139703521
|
A | T | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0168others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+4585T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139703521 | ||||||
| chrX:139703659
|
T | C | 1 | a0001c0003t0001g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-45+4447A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139703659 | ||||||
| chrX:139703704
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-45+4402G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139703704 | ||||||
| chrX:139703872
|
G | T | 1 | a0001c0003t0001g0037 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-45+4234C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139703872 | ||||||
| chrX:139703950
|
GA | G | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+4155delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139703950 | ||||||
| chrX:139704004
|
A | G | 23 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(20): Show | 23 | HG01952.hp1 HG02004.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-45+4102T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704004 | ||||||
| chrX:139704071
|
A | AG | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+4034dupC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704071 | ||||||
| chrX:139704082
|
C | CA | 23 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(20): Show | 23 | HG01952.hp1 HG02004.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-45+4023dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704082 | ||||||
| chrX:139704091
|
A | G | 123 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0027others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.-45+4015T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704091 | ||||||
| chrX:139704342
|
A | T | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+3764T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704342 | ||||||
| chrX:139704598
|
GA | G | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+3507delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704598 | ||||||
| chrX:139704639
|
C | T | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(3): Show | 6 | NA18952.hp1 NA18954.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+3467G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704639 | ||||||
| chrX:139704734
|
AG | A | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+3371delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704734 | ||||||
| chrX:139704860
|
G | A | 123 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0027others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.-45+3246C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704860 | ||||||
| chrX:139704878
|
G | GA | 4 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0001g0161others(1): Show | 4 | HG02615.hp1 HG02615.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+3227dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704878 | ||||||
| chrX:139704878
|
GA | G | 1 | a0001c0001t0001g0029 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-45+3227delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704878 | ||||||
| chrX:139705236
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-45+2870G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139705236 | ||||||
| chrX:139705342
|
C | T | 130 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0016others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-45+2764G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139705342 | ||||||
| chrX:139705841
|
C | T | 2 | a0001c0001t0001g0027a0003c0007t0001g0026 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.-45+2265G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139705841 | ||||||
| chrX:139705924
|
C | T | 34 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(31): Show | 34 | HG01261.hp1 HG01496.hp2 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-45+2182G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139705924 | ||||||
| chrX:139706140
|
C | T | 130 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-45+1966G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706140 | ||||||
| chrX:139706217
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0002t0001g0235 | 3 | HG00639.hp2 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-45+1889C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706217 | ||||||
| chrX:139706485
|
C | T | 1 | a0001c0003t0001g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-45+1621G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706485 | ||||||
| chrX:139706569
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-45+1537C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706569 | ||||||
| chrX:139706724
|
AT | A | 1 | a0004c0009t0001g0024 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-45+1381delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706724 | ||||||
| chrX:139706888
|
A | AATT | 2 | a0001c0001t0001g0023a0004c0009t0001g0024 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-45+1215_-45+1217d others(5): Show |
MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706888 | ||||||
| chrX:139706925
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG01109.hp1 HG02145.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+1181G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706925 | ||||||
| chrX:139706960
|
A | C | 1 | a0001c0001t0001g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-45+1146T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706960 | ||||||
| chrX:139706962
|
A | G | 1 | a0001c0002t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-45+1144T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706962 | ||||||
| chrX:139706971
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-45+1135C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706971 | ||||||
| chrX:139707020
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-45+1086C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139707020 | ||||||
| chrX:139707024
|
C | T | 2 | a0001c0001t0001g0014a0001c0003t0001g0246 | 2 | HG00099.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-45+1082G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139707024 | ||||||
| chrX:139707144
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG02273.hp1 HG02523.hp2 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45+962G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139707144 | ||||||
| chrX:139707426
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00408.hp2 HG02040.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-45+680A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139707426 | ||||||
| chrX:139707487
|
TG | T | 1 | a0001c0001t0001g0004 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+618delC | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139707487 | ||||||
| chrX:139707615
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-45+491A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139707615 | ||||||
| chrX:139707950
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-45+156C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139707950 | ||||||
| chrX:139708049
|
AC | A | 1 | a0001c0003t0001g0246 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-45+56delG | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139708049 |