Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 244 | 67 | 44 | 102 | 7 | 22 | 81 | MCF2_chrX_139576770_139713167 | MCF2 | MQDIA others(996): Show |
chrX | 139576770 | 139713167 |
| a0002 | 0/0 | 1001 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | MQDIA others(996): Show |
chrX | 139576770 | 139713167 |
| a0003 | 0/0 | 1001 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | MQDIA others(996): Show |
chrX | 139576770 | 139713167 |
| a0004 | 0/0 | 1001 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | MQDIA others(996): Show |
chrX | 139576770 | 139713167 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3003 | 186 | 54 | 30 | 80 | 4 | 17 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 | ||
| a0001c0002 | 0/0 | 3003 | 29 | 10 | 4 | 15 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 | ||
| a0001c0003 | 0/1 | 3003 | 24 | 0 | 10 | 5 | 3 | 5 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 | ||
| a0001c0005 | 0/0 | 3003 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 | ||
| a0001c0006 | 0/0 | 3003 | 2 | 0 | 0 | 2 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 | ||
| a0001c0009 | 0/0 | 3003 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 | ||
| a0002c0004 | 0/0 | 3003 | 3 | 3 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 | ||
| a0003c0007 | 0/0 | 3003 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 | ||
| a0004c0008 | 0/0 | 3003 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | ATGCA others(2998): Show |
chrX | 139576770 | 139713167 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3813 | 177 | 50 | 30 | 75 | 4 | 17 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0001t0002 | 0/0 | 3813 | 5 | 0 | 0 | 5 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0001t0004 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0001t0005 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0001t0006 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0001t0007 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0002t0001 | 0/0 | 3813 | 29 | 10 | 4 | 15 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0003t0001 | 0/1 | 3813 | 24 | 0 | 10 | 5 | 3 | 5 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0005t0001 | 0/0 | 3813 | 2 | 2 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0006t0001 | 0/0 | 3813 | 2 | 0 | 0 | 2 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0001c0009t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0002c0004t0003 | 0/0 | 3813 | 3 | 3 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0003c0007t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
chrX | 139576770 | 139713167 |
| a0004c0008t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | GTACA others(3808): Show |
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 |
| 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 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0037 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0065 | 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 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0080 | 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 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0093 | 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 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0125 | 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 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0160 | 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 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0165 | 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 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0171 | 1/0 | 1 | 0 | 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 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0178 | 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 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0185 | 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 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0218 | 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 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0222 | 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 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0002g0104 | 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 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0001t0006g0168 | 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 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0129 | 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 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0153 | 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 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0002t0001g0236 | 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 |
| a0001c0003t0001g0013 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0003t0001g0036 | 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 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0001c0009t0001g0066 | 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 |
| a0002c0004t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0002c0004t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0003c0007t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| a0004c0008t0001g0024 | 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 | g0050 | 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 | g0108 | EUR | GBR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0063 | EUR | FIN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0098 | 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 | g0201 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0139 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | CHS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0060 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0036 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0013 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0090 | 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 | g0135 | 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 | g0091 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0103 | 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 | g0195 | AMR | PUR | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0081 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0137 | 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 | g0198 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0095 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0089 | 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 | g0211 | 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 | g0053 | EUR | IBS | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01884 | hp1 | a0002 | c0004 | t0003 | g0167 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0207 | 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 | g0122 | 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 | g0239 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0197 | 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 | g0105 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0228 | 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 | g0227 | EAS | KHV | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0242 | 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 | g0136 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0088 | 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 | g0151 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0179 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02451 | hp2 | a0003 | c0007 | t0001 | g0155 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0057 | 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 | g0174 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0164 | 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 | g0190 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0061 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0208 | 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 | g0165 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0173 | 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 | g0180 | 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 | g0236 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0170 | 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 | g0117 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0130 | 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 | g0160 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03139 | hp1 | a0001 | c0009 | t0001 | g0066 | AFR | ESN | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0029 | 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 | g0175 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03225 | hp1 | a0004 | c0008 | 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 | g0158 | 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 | g0115 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0102 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0078 | SAS | STU | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0131 | 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 | g0189 | SAS | BEB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0127 | 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 | g0126 | SAS | STU | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | 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 | g0045 | EAS | CHB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | YRI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0156 | AFR | YRI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0076 | 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 | g0065 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18953 | hp1 | a0001 | c0006 | t0001 | g0225 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0005 | 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 | g0118 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0230 | 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 | g0235 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0219 | 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 | g0058 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0082 | 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 | g0084 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0200 | 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 | g0229 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19001 | hp2 | a0001 | c0006 | t0001 | g0226 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0220 | 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 | g0216 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0187 | 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 | g0241 | AFR | LWK | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0096 | 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 | g0085 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0213 | 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 | g0041 | AFR | ASW | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | GIH | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0138 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0154 | AFR | ACB | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | 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 | g0159 | AFR | USA | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0157 | 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 | g0194 | AFR | USA | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | USA | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0168 | AFR | LWK | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0186 | REF | REF | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0171 | REF | REF | MCF2_chrX_139576770_139713167 | MCF2 | chrX | 139576770 | 139713167 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:139582493 | G | A | 1 | a0003 | 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: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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX: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 | a0001c0003 a0004c0008 |
24 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(21): 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 | a0001c0009 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX: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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:139582781 | A | G | 1 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0206 a0001c0001t0001g0210 a0001c0001t0001g0212 |
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 | a0001c0002t0001g0236 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0146 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | 96 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(93): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0072 others(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 | CT | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0074 others(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 | CTTTTT | C | 21 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0142 a0001c0001t0001g0150 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0145 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0001t0001g0195 |
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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0002g0202 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0103 | 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 | a0002c0004t0003g0166 a0002c0004t0003g0167 a0002c0004t0003g0190 |
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 | 35 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0029 others(32): Show |
36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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: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 | a0001c0001t0001g0091 | 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 | a0001c0002t0001g0056 | 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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139586599 | T | A | 1 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0146 |
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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0240 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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:139587414 | G | GA | 7 | a0001c0001t0001g0026 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0003t0001g0138 | 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 | a0001c0001t0001g0228 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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:139587867 | T | TCA | 4 | a0001c0001t0001g0062 a0001c0001t0001g0137 a0001c0001t0001g0211 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0001g0140 others(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:139588166 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2677+194A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 25/28 | chrX | 139588166 | |||||||
| chrX:139588572 | C | T | 1 | a0001c0003t0001g0117 | 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 | a0001c0001t0001g0183 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2599-135C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588573 | |||||||
| chrX:139588683 | G | T | 9 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0142 others(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:139588743 | T | TCTA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0001t0001g0164 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): 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 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0175 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | a0001c0002t0001g0219 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0032 others(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:139588762 | C | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0020 others(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 | 10 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0001t0001g0164 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(7): 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 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0175 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0165 a0001c0001t0001g0173 others(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 | a0001c0002t0001g0143 a0001c0003t0001g0025 |
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:139588844 | C | A | 1 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0122 a0001c0001t0001g0205 others(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:139588941 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2599-503T>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 24/28 | chrX | 139588941 | |||||||
| chrX:139588973 | A | T | 29 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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:139589057 | A | C | 2 | a0001c0002t0001g0223 a0001c0002t0001g0224 |
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:139589180 | G | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0007g0068 |
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:139589430 | T | C | 22 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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:139589958 | C | A | 1 | a0001c0002t0001g0236 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0184 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0146 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | TAA | 18 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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:139590476 | A | AT | 8 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0131 | 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 | 30 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0161 others(27): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.2506-609C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139590536 | |||||||
| chrX:139590549 | CTTCCTTA | C | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): 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 | 96 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(93): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139591715 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0137 |
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 | a0001c0001t0001g0126 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0136 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0044 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0003t0001g0108 | 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 | a0001c0001t0001g0193 | 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 | a0004c0008t0001g0024 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0174 a0001c0005t0001g0154 a0001c0005t0001g0156 |
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 | a0001c0003t0001g0081 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0079 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0238 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0083 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | 96 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(93): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): 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 | a0001c0001t0001g0213 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0115 | 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 | a0001c0002t0001g0236 | 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 | a0001c0002t0001g0236 | 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 | a0001c0002t0001g0223 | 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 | a0001c0001t0001g0059 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2505+1032T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 23/28 | chrX | 139595517 | |||||||
| chrX:139595595 | G | A | 7 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0051 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0145 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0208 | 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 | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(236): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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:139596926 | C | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0146 others(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:139596995 | T | C | 18 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0003t0001g0002 a0001c0003t0001g0198 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0054 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2283+87C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 22/28 | chrX | 139597373 | |||||||
| chrX:139597610 | T | C | 7 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(153): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0176 a0001c0001t0001g0194 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0099 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2065-887C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599385 | |||||||
| chrX:139599409 | C | T | 6 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0153 | 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 | 30 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0161 others(27): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.2065-1224G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 20/28 | chrX | 139599722 | |||||||
| chrX:139599797 | T | G | 1 | a0001c0002t0001g0236 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0142 others(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:139600273 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0176 a0001c0001t0001g0194 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0175 | 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 | a0001c0009t0001g0066 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0003t0001g0138 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0188 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0003t0001g0047 a0001c0003t0001g0113 a0001c0003t0001g0114 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
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 | a0001c0003t0001g0049 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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:139602293 | C | T | 7 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0159 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0153 | 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 | 30 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0161 others(27): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): 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 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0064 a0001c0001t0001g0101 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0009t0001g0066 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0042 others(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 | 71 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0120 others(68): Show |
72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1971+361dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 19/28 | chrX | 139604319 | |||||||
| chrX:139604319 | C | CAA | 15 | a0001c0001t0001g0022 a0001c0002t0001g0015 a0001c0002t0001g0056 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0005t0001g0154 a0001c0005t0001g0156 |
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 | a0001c0002t0001g0177 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1901+54C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 18/28 | chrX | 139604815 | |||||||
| chrX:139605156 | CT | C | 93 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1786-173delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 17/28 | chrX | 139605156 | |||||||
| chrX:139605156 | CTT | C | 8 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0160 others(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 | a0001c0009t0001g0066 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 28 | a0001c0001t0001g0161 a0001c0001t0001g0169 a0001c0001t0001g0174 others(25): Show |
29 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(26): 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:139606381 | G | A | 1 | a0001c0001t0001g0244 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0007 | 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 | a0001c0001t0001g0207 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | a0001c0001t0001g0176 | 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 | a0001c0002t0001g0236 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0214 |
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 | 30 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0161 others(27): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.1718+146A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 16/28 | chrX | 139607545 | |||||||
| chrX:139607932 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0238 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0169 a0001c0002t0001g0015 a0001c0002t0001g0143 others(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 | a0001c0005t0001g0154 a0001c0005t0001g0156 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0220 |
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 | a0001c0001t0002g0203 | 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 | a0001c0003t0001g0002 a0001c0003t0001g0198 |
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:139609104 | C | T | 1 | a0001c0001t0002g0203 | 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 | a0001c0001t0001g0101 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1629+1160C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139609141 | |||||||
| chrX:139609279 | T | A | 1 | a0001c0001t0001g0187 | 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 | a0001c0009t0001g0066 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1629+1010A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 15/28 | chrX | 139609291 | |||||||
| 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: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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0161 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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:139611980 | G | A | 48 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(45): Show |
49 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(46): 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 | GA | G | 8 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0143 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0236 |
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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0238 |
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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0142 others(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 | a0001c0003t0001g0063 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | ATG | A | 12 | a0001c0001t0001g0044 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | ATGTGTGT others(1): Show |
A | 9 | a0001c0001t0001g0091 a0001c0001t0001g0134 a0001c0001t0001g0187 others(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 | 151 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(148): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): 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 | a0001c0001t0001g0161 a0001c0002t0001g0236 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0022 a0002c0004t0003g0166 a0002c0004t0003g0167 others(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 | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): 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 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0136 others(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:139615374 | G | A | 2 | a0001c0002t0001g0223 a0001c0002t0001g0224 |
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 | a0001c0009t0001g0066 | 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 | 94 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1180-21delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 11/28 | chrX | 139616493 | |||||||
| chrX:139616493 | GAA | G | 5 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0160 others(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 | 94 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): 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 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0001t0001g0054 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0045 | 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 | 33 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0074 others(30): Show |
34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.988-147dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139617850 | |||||||
| chrX:139618131 | C | G | 5 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | 91 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.988-553G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 10/28 | chrX | 139618257 | |||||||
| chrX:139618417 | C | T | 23 | a0001c0003t0001g0002 a0001c0003t0001g0013 a0001c0003t0001g0025 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(21): 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0150 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0146 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0001t0004g0209 | 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 | a0001c0001t0001g0161 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0126 | 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 | a0001c0002t0001g0103 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0001g0189 others(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 | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0192 others(1): Show |
4 | HG01123.hp2 HG01346.hp2 HG02717.hp1 others(1): 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 | a0001c0003t0001g0013 a0001c0003t0001g0061 a0001c0003t0001g0139 |
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 | a0001c0001t0001g0170 a0001c0001t0001g0195 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0125 a0001c0001t0001g0130 others(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:139620025 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0241 a0001c0002t0001g0236 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0125 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0002t0001g0141 others(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 | GTGTGTGT others(3): Show |
5 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | 24 | a0001c0001t0001g0239 a0001c0003t0001g0002 a0001c0003t0001g0013 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): 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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | a0001c0001t0001g0022 a0002c0004t0003g0166 a0002c0004t0003g0167 others(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 | a0001c0005t0001g0154 a0001c0005t0001g0156 |
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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0079 | 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 | a0001c0002t0001g0008 a0001c0002t0001g0055 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0236 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0161 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0045 others(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:139623116 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0238 |
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:139623658 | C | T | 1 | a0001c0009t0001g0066 | 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 | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.867+2527C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623666 | |||||||
| chrX:139623667 | TAA | T | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): 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 | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): 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 | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.867+2511C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623682 | |||||||
| chrX:139623683 | T | A | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.867+2510A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139623683 | |||||||
| chrX:139623684 | A | C | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): 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 | a0001c0003t0001g0002 a0001c0003t0001g0198 |
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 | a0001c0001t0001g0174 | 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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.867+1750C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 9/28 | chrX | 139624443 | |||||||
| chrX:139624531 | CA | C | 14 | a0001c0001t0001g0130 a0001c0001t0001g0145 a0001c0001t0001g0161 others(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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0176 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0236 |
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 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0094 a0001c0001t0001g0146 others(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 | a0001c0005t0001g0154 a0001c0005t0001g0156 |
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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0143 others(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 | a0001c0001t0001g0213 | 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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0143 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0130 others(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 | a0001c0003t0001g0047 a0001c0003t0001g0113 a0001c0003t0001g0114 others(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:139626864 | T | G | 5 | a0001c0002t0001g0015 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0196 | 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 | 95 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): 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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0001t0001g0217 | 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 | a0001c0002t0001g0058 a0001c0002t0001g0152 |
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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0143 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0161 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0015 a0001c0002t0001g0141 others(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 | a0001c0005t0001g0154 a0001c0005t0001g0156 |
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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0174 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0022 a0002c0004t0003g0166 a0002c0004t0003g0167 others(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 | 88 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): 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 | a0001c0001t0001g0116 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0045 others(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 | 83 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.468+90dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 6/28 | chrX | 139631304 | |||||||
| chrX:139631516 | A | G | 11 | a0001c0001t0001g0161 a0001c0002t0001g0141 a0001c0002t0001g0143 others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0030 others(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 | 84 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): 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 | a0001c0001t0001g0022 a0002c0004t0003g0166 a0002c0004t0003g0167 others(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 | a0001c0002t0001g0153 | 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 | 91 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): 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 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0141 a0001c0002t0001g0143 others(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 | a0001c0001t0001g0169 | 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 | a0004c0008t0001g0024 | 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 | a0001c0001t0002g0202 | 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 | a0001c0002t0001g0008 a0001c0002t0001g0055 |
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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0146 |
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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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: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 | a0001c0001t0001g0242 | 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 | 80 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(77): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): 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 | a0001c0001t0001g0076 | 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 | a0001c0002t0001g0153 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0001t0001g0230 |
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 | a0001c0001t0001g0026 | 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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0009t0001g0066 | 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 | 80 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(77): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(78): 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 | a0001c0001t0001g0161 a0001c0002t0001g0141 a0001c0002t0001g0143 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0161 | 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 | 84 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): 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 | a0001c0001t0001g0213 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.232-3089C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139635543 | |||||||
| chrX:139635664 | T | A | 82 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): 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 | a0001c0001t0001g0094 a0001c0001t0001g0188 |
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 | 85 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): 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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | 85 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): 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 | a0001c0003t0001g0063 | 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 | 85 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): 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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | 91 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): 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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 others(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 | 85 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): 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 | a0001c0001t0001g0169 | 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 | 69 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0089 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.232-3856A>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139636310 | |||||||
| chrX:139636333 | T | G | 86 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): 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 | a0001c0002t0001g0236 | 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 | 85 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): 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 | a0001c0002t0001g0236 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | 96 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(93): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): 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 | a0001c0001t0001g0161 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0001t0001g0161 a0001c0002t0001g0143 a0001c0002t0001g0157 others(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 | a0001c0003t0001g0108 | 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 | a0001c0002t0001g0236 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0001t0001g0161 others(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 | a0001c0002t0001g0236 | 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 | a0001c0001t0001g0022 a0002c0004t0003g0166 a0002c0004t0003g0167 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0238 |
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 | 87 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0062 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.232-5867A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139638321 | |||||||
| chrX:139638544 | T | C | 87 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0062 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): 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 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0238 |
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 | 77 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0062 others(74): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0238 others(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 | a0001c0001t0001g0022 a0001c0002t0001g0141 a0001c0002t0001g0159 others(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 | 87 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0062 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): 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 | a0001c0001t0001g0237 | 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 | 87 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0062 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.231+6431T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139639137 | |||||||
| chrX:139639201 | A | G | 83 | a0001c0001t0001g0018 a0001c0001t0001g0062 a0001c0001t0001g0064 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
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 | 83 | a0001c0001t0001g0018 a0001c0001t0001g0062 a0001c0001t0001g0064 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): 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 | a0001c0002t0001g0153 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0238 |
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 | 69 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0089 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(67): 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 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0065 others(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 | a0001c0003t0001g0081 | 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 | 24 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0089 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(21): 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0145 others(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 | 85 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0062 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): 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 | a0001c0001t0001g0026 | 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 | a0001c0003t0001g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.231+4813A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139640755 | |||||||
| chrX:139640877 | T | C | 77 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0062 others(74): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): 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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139641170 | A | ATG | 4 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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:139641562 | A | G | 1 | a0001c0001t0001g0237 | 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 | a0001c0003t0001g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.231+3999G>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139641569 | |||||||
| chrX:139641786 | T | C | 4 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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:139642682 | GA | G | 14 | a0001c0001t0001g0094 a0001c0001t0001g0188 a0001c0001t0001g0231 others(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 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0174 a0001c0001t0001g0176 others(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:139643070 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.231+2498T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643070 | |||||||
| chrX:139643140 | G | A | 1 | a0001c0001t0001g0147 | 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 | a0001c0002t0001g0236 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(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:139643417 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.231+2151A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139643417 | |||||||
| chrX:139643624 | G | C | 1 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0188 |
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:139644052 | G | A | 89 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): 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 | a0001c0003t0001g0047 a0001c0003t0001g0113 a0001c0003t0001g0114 others(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 | a0001c0001t0001g0085 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.231+1135A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 4/28 | chrX | 139644433 | |||||||
| 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 | a0001c0001t0001g0043 | 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 | a0001c0002t0001g0141 a0001c0002t0001g0159 a0001c0002t0001g0162 others(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 | a0002c0004t0003g0190 | 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 | 94 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): 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 | a0001c0002t0001g0159 | 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 | a0001c0001t0001g0100 | 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 | a0001c0003t0001g0036 a0001c0003t0001g0050 a0001c0003t0001g0063 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(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 | a0001c0002t0001g0159 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(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 | 34 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0062 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.140+478C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 3/28 | chrX | 139646311 | |||||||
| chrX:139647333 | A | G | 1 | a0001c0002t0001g0058 | 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 | 25 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0080 others(22): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(22): 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 | a0001c0001t0001g0022 a0001c0001t0001g0238 a0001c0005t0001g0154 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0044 | 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 | a0001c0001t0002g0104 a0001c0001t0002g0200 a0001c0001t0002g0203 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0002t0001g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.26-1234G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139648137 | |||||||
| chrX:139648385 | C | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0101 |
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 | 94 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0044 | 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 | 134 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.25+2074delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649645 | |||||||
| chrX:139649649 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.25+2071T>C | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649649 | |||||||
| chrX:139649819 | C | G | 63 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(60): Show |
63 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(60): 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(135): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.25+1795A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139649925 | |||||||
| chrX:139650130 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0238 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0221 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0107 | 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 | a0001c0002t0001g0103 | 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 | 66 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(63): Show |
66 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(63): 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 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0142 a0001c0001t0001g0144 others(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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0018 others(88): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): 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 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0029 others(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:139651095 | C | T | 31 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0064 others(28): Show |
32 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(29): 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 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0125 others(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:139651137 | G | A | 71 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0018 others(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 | a0001c0003t0001g0117 | 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 | a0001c0003t0001g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+530T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 2/28 | chrX | 139651190 | |||||||
| chrX:139651305 | G | C | 1 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0161 | 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 | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(52): Show |
58 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(55): 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 | a0001c0001t0001g0019 a0001c0002t0001g0153 a0001c0005t0001g0154 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(59): Show |
65 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(62): 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0223 | 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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(84): Show |
90 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(87): 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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:139652940 | C | A | 1 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0003t0001g0060 a0001c0003t0001g0061 a0001c0003t0001g0139 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(67): Show |
73 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.-44-1625C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139653413 | |||||||
| chrX:139653548 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(71): Show |
77 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(74): 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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: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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0130 | 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 | 52 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(49): Show |
55 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(52): 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 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0170 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139655693 | G | A | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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: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 | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(58): Show |
64 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(61): 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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(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 | a0001c0002t0001g0058 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-44-4973G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139656761 | |||||||
| chrX:139657261 | C | T | 3 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0096 a0001c0002t0001g0097 |
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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0169 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0160 | 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 | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(80): Show |
86 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.-44-6553delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139658340 | |||||||
| chrX:139658667 | G | GT | 41 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0030 others(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 | GTTTTTTT others(1): Show |
7 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0140 others(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 | GT | G | 12 | a0001c0001t0001g0016 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0169 a0002c0004t0003g0166 a0002c0004t0003g0167 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0002t0001g0199 | 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 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
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:139659322 | A | T | 1 | a0001c0002t0001g0159 | 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 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0007g0068 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0148 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0064 | 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 | a0001c0003t0001g0139 | 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 | a0001c0001t0005g0179 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0002t0001g0157 | 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 | a0001c0002t0001g0143 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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:139662597 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-44-10809C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662597 | |||||||
| chrX:139662951 | C | T | 3 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0044 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-44-11181G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139662969 | |||||||
| chrX:139663393 | TGTAA | T | 3 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0164 others(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:139663577 | T | G | 1 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0053 a0001c0001t0001g0122 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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:139664321 | A | AAAC | 6 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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:139664331 | A | C | 4 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0006t0001g0225 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0070 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0089 others(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 | 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 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0126 others(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:139665899 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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:139665901 | A | G | 33 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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: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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0130 others(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:139665924 | TATAC | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0009t0001g0066 |
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 | 35 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(32): Show |
37 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(34): 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 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(46): Show |
52 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(49): 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139666468 | T | G | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0246 a0001c0001t0002g0104 |
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:139666575 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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:139666886 | A | C | 1 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | CT | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(62): Show |
68 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.-44-15409delA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139667196 | |||||||
| chrX:139667196 | CTT | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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:139667250 | G | A | 1 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
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 | a0001c0002t0001g0162 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0006t0001g0225 others(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:139667828 | G | A | 1 | a0001c0003t0001g0114 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0007g0068 |
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 | a0001c0002t0001g0199 | 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 | a0001c0001t0001g0187 | 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 | a0001c0002t0001g0199 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-44-16311G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668099 | |||||||
| chrX:139668268 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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:139668284 | C | T | 1 | a0001c0001t0001g0237 | 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 | 52 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(49): Show |
55 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.-44-16516A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668304 | |||||||
| chrX:139668416 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(45): Show |
51 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.-44-16628C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139668416 | |||||||
| chrX:139668518 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(85): Show |
91 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(88): 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0002t0001g0236 |
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:139668859 | T | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0229 others(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:139669101 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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:139669131 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0150 |
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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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:139669891 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0232 |
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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139670389 | T | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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 | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(47): Show |
53 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(50): 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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0243 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0002t0001g0236 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139671582 | A | G | 10 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(82): Show |
88 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(85): 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139672123 | C | A | 30 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0222 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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 | a0001c0001t0001g0127 | 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 | a0001c0005t0001g0154 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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:139673354 | C | T | 10 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0189 | 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 | a0001c0003t0001g0113 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0002t0001g0157 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0003t0001g0013 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0196 | 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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0004g0209 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0181 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0160 a0001c0002t0001g0159 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0002t0001g0004 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0089 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-44-24442G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139676230 | |||||||
| 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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:139677958 | T | A | 1 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0169 others(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:139678082 | G | T | 1 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0080 | 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 | a0001c0002t0001g0162 | 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 | 58 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
58 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(55): 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 | a0001c0003t0001g0036 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0229 |
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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0235 | 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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0062 a0001c0001t0001g0112 |
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 | a0001c0001t0001g0140 a0001c0001t0001g0170 a0001c0002t0001g0141 |
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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(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 | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(48): Show |
54 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(51): 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0003t0001g0113 a0001c0003t0001g0114 |
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 | a0001c0001t0001g0170 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-45+25270G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139682836 | |||||||
| chrX:139682990 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0002t0001g0153 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0002t0001g0236 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0181 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0216 a0001c0001t0001g0217 others(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 | a0001c0002t0001g0197 a0001c0003t0001g0002 a0001c0003t0001g0198 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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:139685164 | C | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
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 | a0001c0002t0001g0056 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0160 a0001c0002t0001g0159 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0140 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 |
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:139686031 | C | T | 3 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0216 a0001c0002t0001g0224 |
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 | 36 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0020 others(33): Show |
36 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.-45+22035delT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139686070 | |||||||
| chrX:139686070 | TAA | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(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:139686083 | A | C | 1 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0140 a0001c0002t0001g0141 |
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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0187 | 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 | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): 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:139687191 | A | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0002t0001g0236 |
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 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0181 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(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 | 29 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0130 others(26): Show |
29 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(26): 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 | a0001c0001t0001g0119 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0142 a0001c0001t0001g0150 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
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 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0120 a0001c0003t0001g0138 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(64): Show |
70 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(67): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(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:139688909 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0178 a0001c0001t0001g0180 others(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:139689302 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): 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 | a0001c0003t0001g0081 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0136 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-45+18409G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139689697 | |||||||
| chrX:139689991 | C | A | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0176 others(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 | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(63): Show |
69 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.-45+17887dupT | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139690218 | |||||||
| chrX:139690229 | T | C | 1 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(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 | 135 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): 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 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0002t0001g0015 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
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 | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(47): Show |
53 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(50): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-45+16504A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139691602 | |||||||
| chrX:139691730 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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:139692050 | C | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(237): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): 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 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0070 a0001c0001t0001g0071 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0212 | 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 | a0001c0003t0001g0036 a0001c0003t0001g0050 |
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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0187 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(57): Show |
63 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(60): 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 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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:139694383 | C | T | 1 | a0001c0002t0001g0159 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-45+13723G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139694383 | |||||||
| chrX:139694405 | G | GA | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(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:139694953 | A | G | 1 | a0001c0003t0001g0013 | 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 | a0001c0002t0001g0162 | 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 | 25 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0057 others(22): Show |
25 | HG00673.hp1 HG01261.hp1 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.-45+13073dupA | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139695032 | |||||||
| chrX:139695032 | CT | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-45+11896A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139696210 | |||||||
| chrX:139696280 | CCCTT | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0052 others(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 | TTTCTC | 147 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 |
26 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0057 others(23): Show |
26 | HG00673.hp1 HG02071.hp1 HG02083.hp1 others(23): 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 | a0001c0002t0001g0058 a0001c0002t0001g0152 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0003t0001g0060 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0178 others(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:139697394 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0178 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(221): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): 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 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0192 others(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:139697997 | G | C | 3 | a0001c0002t0001g0143 a0001c0002t0001g0157 a0001c0002t0001g0158 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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:139698155 | A | AAAAATAA others(9): Show |
1 | a0001c0003t0001g0050 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0172 others(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 | a0001c0003t0001g0049 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0169 | 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 | a0001c0002t0001g0129 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-45+8599C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699507 | |||||||
| chrX:139699586 | G | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
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 | a0001c0001t0001g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-45+8499C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139699607 | |||||||
| chrX:139699983 | G | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0178 others(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 | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-45+8076C>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700030 | |||||||
| 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:139700543 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-45+7563G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139700543 | |||||||
| 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0163 others(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:139701032 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-45+7074G>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701032 | |||||||
| chrX:139701087 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
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:139701361 | G | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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:139701490 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+6616G>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701490 | |||||||
| chrX:139701947 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-45+6159C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139701947 | |||||||
| chrX:139702113 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-45+5993A>G | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702113 | |||||||
| chrX:139702608 | A | T | 1 | a0001c0001t0001g0038 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5498T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139702608 | |||||||
| chrX:139702875 | C | A | 6 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0140 a0001c0002t0001g0141 |
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 | a0001c0003t0001g0138 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0169 others(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 | a0001c0003t0001g0139 | 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 | a0001c0001t0001g0037 | 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 | a0001c0003t0001g0036 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-45+4234C>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139703872 | |||||||
| chrX:139704004 | A | G | 23 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(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:139704082 | C | CA | 23 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0163 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-45+3764T>A | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139704342 | |||||||
| chrX:139704639 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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:139704860 | G | A | 123 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0026 others(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: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 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0002t0001g0236 |
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 | a0001c0001t0001g0239 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-45+1537C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139706569 | |||||||
| chrX:139706888 | A | AATT | 2 | a0001c0001t0001g0023 a0004c0008t0001g0024 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0014 a0001c0003t0001g0013 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 |
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:139707615 | T | C | 1 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-45+156C>T | MCF2 | ENSG00000101977.22 | transcript | ENST00000519895.6 | protein_coding | 1/28 | chrX | 139707950 |