Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6611 |
|---|---|
| ensemblid | ENSG00000102172.16 |
| hgncid | 11123 |
| symbol | SMS |
| name | spermine synthase |
| refseq_nuc | NM_004595.5 |
| refseq_prot | NP_004586.2 |
| ensembl_nuc | ENST00000404933.7 |
| ensembl_prot | ENSP00000385746.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 21940709 |
| end | 21994837 |
| strand | + |
| ver | v1.2 |
| region | chrX:21940709-21994837 |
| region5000 | chrX:21935709-21999837 |
| regionname0 | SMS_chrX_21940709_21994837 |
| regionname5000 | SMS_chrX_21935709_21999837 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 366 | 295 | 74 | 48 | 128 | 13 | 30 | 94 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0002 | 0/0 | 366 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0003 | 0/0 | 366 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0004 | 0/0 | 366 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1101 | 292 | 73 | 46 | 128 | 13 | 30 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| c0002 | 0/0 | 1101 | 2 | 0 | 2 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| c0003 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| c0004 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| c0005 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| c0006 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 603 | 129 | 8 | 24 | 75 | 6 | 14 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0002 | 0/0 | 603 | 69 | 21 | 7 | 28 | 3 | 10 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0003 | 0/0 | 602 | 40 | 27 | 8 | 1 | 1 | 3 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0004 | 0/0 | 602 | 24 | 12 | 5 | 3 | 2 | 2 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0005 | 0/0 | 603 | 17 | 2 | 2 | 12 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0006 | 0/0 | 603 | 7 | 3 | 0 | 3 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0007 | 0/0 | 604 | 4 | 0 | 1 | 3 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0008 | 0/0 | 602 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0009 | 0/0 | 602 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0010 | 0/0 | 604 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0011 | 0/0 | 609 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0012 | 0/0 | 603 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0013 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0014 | 0/0 | 602 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| t0015 | 0/0 | 604 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1101 | 292 | 73 | 46 | 128 | 13 | 30 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0002 | 0/0 | 1101 | 2 | 0 | 2 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0005 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0002c0003 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0003c0006 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0004c0004 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1703 | 127 | 7 | 24 | 74 | 6 | 14 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0002 | 0/0 | 1703 | 68 | 21 | 7 | 27 | 3 | 10 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0003 | 0/0 | 1702 | 38 | 27 | 6 | 1 | 1 | 3 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0004 | 0/0 | 1702 | 24 | 12 | 5 | 3 | 2 | 2 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0005 | 0/0 | 1703 | 17 | 2 | 2 | 12 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0006 | 0/0 | 1703 | 7 | 3 | 0 | 3 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0007 | 0/0 | 1704 | 4 | 0 | 1 | 3 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0008 | 0/0 | 1702 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0009 | 0/0 | 1702 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0010 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0011 | 0/0 | 1709 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0012 | 0/0 | 1703 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0014 | 0/0 | 1702 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0001t0015 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0002t0003 | 0/0 | 1702 | 2 | 0 | 2 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0001c0005t0001 | 0/0 | 1703 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0002c0003t0002 | 0/0 | 1703 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0003c0006t0001 | 0/0 | 1703 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| a0004c0004t0013 | 0/0 | 1705 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | copy fasta | chrX | 21935709 | 21999837 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0007g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0008g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0009g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0010g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0012g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0001t0015g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0001c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0002c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0003c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| a0004c0004t0013g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0197 | EUR | GBR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0083 | EUR | GBR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | GBR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0138 | EUR | FIN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00438 | hp1 | a0001 | c0001 | t0006 | g0046 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00438 | hp2 | a0003 | c0006 | t0001 | g0230 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0261 | EAS | CHS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0169 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0272 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0273 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0102 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0063 | EUR | IBS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0064 | EUR | IBS | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0239 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02080 | hp2 | a0001 | c0001 | t0015 | g0004 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CDX | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CDX | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CDX | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02273 | hp2 | a0001 | c0001 | t0012 | g0048 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0139 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0219 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0119 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | STU | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | BEB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | BEB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0264 | SAS | BEB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | STU | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | STU | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | STU | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | YRI | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | YRI | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | YRI | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18961 | hp1 | a0001 | c0001 | t0010 | g0255 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0237 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18978 | hp2 | a0004 | c0004 | t0013 | g0293 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18992 | hp2 | a0001 | c0001 | t0014 | g0213 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0047 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19006 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | LWK | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | LWK | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0283 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0282 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19082 | hp1 | a0001 | c0001 | t0007 | g0286 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19084 | hp1 | a0001 | c0001 | t0007 | g0226 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19089 | hp2 | a0002 | c0003 | t0002 | g0193 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | YRI | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | YRI | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ASW | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0167 | EUR | TSI | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | MSL | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | USA | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | USA | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0266 | EAS | JPT | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | USA | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | USA | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0092 | REF | REF | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0059 | REF | REF | SMS_chrX_21935709_21999837 | SMS | chrX | 21935709 | 21999837 |
| 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:21972512
|
G | GA | 1 | a0002 | 1 | NA19089.hp2 | frameshift_variant | HIGH | c.272dupA | p.Asn91fs | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/11 | 389/1703 | 273/1101 | 91/366 | INFO_REALIGN_3_PRIME | chrX | 21972512 | |
| chrX:21978023
|
C | T | 1 | a0003 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.569C>T | p.Thr190Ile | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 6/11 | 685/1703 | 569/1101 | 190/366 | chrX | 21978023 | ||
| chrX:21992671
|
AT | A | 1 | a0004 | 1 | NA18978.hp2 | frameshift_variant | HIGH | c.1024delT | p.Ser342fs | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/11 | 1140/1703 | 1024/1101 | 342/366 | INFO_REALIGN_3_PRIME | chrX | 21992671 | |
| chrX:21994342
|
T | TA | 1 | a0004 | 1 | NA18978.hp2 | frameshift_variant | HIGH | c.1095dupA | p.Pro366fs | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 1212/1703 | 1096/1101 | 366/366 | INFO_REALIGN_3_PRIME | chrX | 21994342 |
| 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:21978015
|
A | G | 1 | a0001c0002 | 2 | HG01081.hp2 HG02293.hp1 |
synonymous_variant | LOW | c.561A>G | p.Glu187Glu | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 6/11 | 677/1703 | 561/1101 | 187/366 | chrX | 21978015 | ||
| chrX:21984396
|
A | G | 1 | a0001c0005 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.843A>G | p.Pro281Pro | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/11 | 959/1703 | 843/1101 | 281/366 | chrX | 21984396 |
| 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:21940733
|
A | G | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(5): Show | 129 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(126): Show |
5_prime_UTR_variant | MODIFIER | c.-92A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/11 | 92 | chrX | 21940733 | |||||
| chrX:21940769
|
G | GC | 2 | a0001c0001t0007a0001c0001t0015 | 5 | HG01981.hp2 HG02080.hp2 NA19006.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-50dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/11 | 49 | INFO_REALIGN_3_PRIME | chrX | 21940769 | ||||
| chrX:21994449
|
T | TC | 1 | a0004c0004t0013 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 101 | INFO_REALIGN_3_PRIME | chrX | 21994449 | ||||
| chrX:21994531
|
GT | G | 2 | a0001c0001t0008a0001c0001t0014 | 2 | NA18970.hp1 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*190delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 190 | INFO_REALIGN_3_PRIME | chrX | 21994531 | ||||
| chrX:21994596
|
A | AC | 5 | a0001c0001t0005a0001c0001t0006a0001c0001t0011others(2): Show | 27 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*253dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 254 | INFO_REALIGN_3_PRIME | chrX | 21994596 | ||||
| chrX:21994602
|
C | T | 1 | a0001c0001t0012 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 251 | chrX | 21994602 | |||||
| chrX:21994645
|
C | CTTTTGT | 1 | a0001c0001t0011 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*310_*315dupTGTTTT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 316 | INFO_REALIGN_3_PRIME | chrX | 21994645 | ||||
| chrX:21994662
|
GT | G | 1 | a0001c0001t0009 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 315 | INFO_REALIGN_3_PRIME | chrX | 21994662 | ||||
| chrX:21994794
|
T | TA | 1 | a0001c0001t0010 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 453 | INFO_REALIGN_3_PRIME | chrX | 21994794 | ||||
| chrX:21994794
|
TA | T | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(4): Show | 90 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*452delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 11/11 | 452 | INFO_REALIGN_3_PRIME | chrX | 21994794 |
| 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:21940905
|
T | TC | 1 | a0001c0001t0001g0002 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.49+36dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21940905 | |||||
| chrX:21940933
|
T | TG | 1 | a0001c0001t0001g0297 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.49+64dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21940933 | |||||
| chrX:21940938
|
C | CG | 2 | a0001c0001t0001g0003a0001c0001t0015g0004 | 2 | HG00597.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.49+70dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21940938 | |||||
| chrX:21940983
|
G | GC | 2 | a0001c0001t0001g0297a0001c0001t0002g0005 | 2 | NA18972.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.49+113dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21940983 | |||||
| chrX:21941030
|
C | CG | 1 | a0001c0001t0001g0296 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.49+161dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941030 | |||||
| chrX:21941045
|
CG | C | 1 | a0001c0001t0002g0005 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.49+174delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941045 | |||||
| chrX:21941078
|
T | TC | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+207dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941078 | |||||
| chrX:21941079
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.49+206C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941079 | ||||||
| chrX:21941155
|
GC | G | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.49+285delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941155 | |||||
| chrX:21941274
|
G | A | 7 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0003g0008others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+401G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941274 | ||||||
| chrX:21941389
|
G | A | 1 | a0001c0001t0006g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.49+516G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941389 | ||||||
| chrX:21941396
|
T | TC | 1 | a0001c0001t0002g0005 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.49+527dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941396 | |||||
| chrX:21941418
|
TG | T | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+549delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941418 | |||||
| chrX:21941464
|
A | G | 6 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(3): Show | 6 | HG03041.hp2 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+591A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941464 | ||||||
| chrX:21941467
|
G | C | 1 | a0001c0001t0001g0015 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.49+594G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941467 | ||||||
| chrX:21941486
|
CG | C | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+615delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941486 | |||||
| chrX:21941548
|
AG | A | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+677delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941548 | |||||
| chrX:21941573
|
A | AC | 1 | a0001c0001t0001g0002 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.49+704dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941573 | |||||
| chrX:21941573
|
AC | A | 1 | a0001c0001t0007g0286 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.49+704delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941573 | |||||
| chrX:21941582
|
C | CG | 1 | a0001c0001t0002g0005 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.49+713dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941582 | |||||
| chrX:21941623
|
A | AC | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+751dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941623 | |||||
| chrX:21941637
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+764A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941637 | ||||||
| chrX:21941657
|
CG | C | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+787delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941657 | |||||
| chrX:21941714
|
G | GT | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+842dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941714 | |||||
| chrX:21941736
|
T | C | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.49+863T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941736 | ||||||
| chrX:21941754
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+881A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941754 | ||||||
| chrX:21941755
|
C | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+882C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941755 | ||||||
| chrX:21941758
|
G | GC | 1 | a0001c0001t0002g0005 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.49+887dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941758 | |||||
| chrX:21941764
|
A | T | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.49+891A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941764 | ||||||
| chrX:21941777
|
C | T | 27 | a0001c0001t0002g0258a0001c0001t0002g0267a0001c0001t0002g0276others(24): Show | 27 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+904C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941777 | ||||||
| chrX:21941826
|
A | T | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+953A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941826 | ||||||
| chrX:21941827
|
GTGAGC | G | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+955_49+959delTG others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941827 | ||||||
| chrX:21941836
|
G | C | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+963G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941836 | ||||||
| chrX:21941839
|
CG | C | 1 | a0001c0001t0001g0006 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.49+967delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941839 | ||||||
| chrX:21941884
|
C | CA | 15 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(12): Show | 15 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+1050dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
C | CAA | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG00741.hp2 HG03710.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1049_49+1050dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
C | CAAA | 3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG00738.hp1 HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.49+1048_49+1050dup others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
C | CAAAAAAA others(2): Show |
1 | a0001c0001t0001g0018 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49+1042_49+1050dup others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CA | C | 29 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0084others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.49+1050delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAA | C | 10 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0002g0007others(7): Show | 10 | HG02486.hp1 HG02630.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+1049_49+1050del others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAA | C | 14 | a0001c0001t0001g0117a0001c0001t0002g0112a0001c0001t0002g0114others(11): Show | 14 | HG00140.hp1 HG01496.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+1048_49+1050del others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAA | C | 29 | a0001c0001t0001g0140a0001c0001t0002g0123a0001c0001t0002g0125others(26): Show | 29 | HG00323.hp1 HG00735.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.49+1047_49+1050del others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAA | C | 20 | a0001c0001t0001g0145a0001c0001t0001g0162a0001c0001t0001g0164others(17): Show | 20 | HG01069.hp1 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.49+1046_49+1050del others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAA | C | 10 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0002g0166others(7): Show | 10 | HG00741.hp1 HG01081.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+1045_49+1050del others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG02683.hp1 HG03017.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+1044_49+1050del others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA others(1): Show |
C | 1 | a0001c0001t0002g0005 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.49+1043_49+1050del others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA others(5): Show |
C | 15 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(12): Show | 15 | HG00597.hp2 HG01361.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+1039_49+1050del others(12): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA others(6): Show |
C | 23 | a0001c0001t0002g0192a0001c0001t0002g0194a0001c0001t0002g0195others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.49+1038_49+1050del others(13): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA others(7): Show |
C | 11 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(8): Show | 11 | HG00544.hp1 HG00673.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+1037_49+1050del others(14): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA others(8): Show |
C | 19 | a0001c0001t0002g0267a0001c0001t0002g0276a0001c0001t0002g0277others(16): Show | 19 | HG00558.hp1 HG00621.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.49+1036_49+1050del others(15): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0002g0220 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.49+1035_49+1050del others(16): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA others(14): Show |
C | 8 | a0001c0001t0001g0002a0001c0001t0001g0222a0001c0001t0001g0223others(5): Show | 8 | HG01978.hp2 HG02293.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+1030_49+1050del others(21): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941884
|
CAAAAAAA others(15): Show |
C | 33 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0228others(30): Show | 33 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.49+1029_49+1050del others(22): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21941884 | |||||
| chrX:21941885
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.49+1012A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941885 | ||||||
| chrX:21941914
|
A | C | 1 | a0001c0001t0003g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.49+1041A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941914 | ||||||
| chrX:21941919
|
A | C | 2 | a0001c0001t0001g0284a0001c0001t0003g0285 | 2 | HG01891.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.49+1046A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941919 | ||||||
| chrX:21941923
|
A | AAAAAAAA others(1): Show |
1 | a0001c0001t0001g0019 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.49+1050_49+1051ins others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21941923 | ||||||
| chrX:21942096
|
C | A | 64 | a0001c0001t0001g0145a0001c0001t0002g0007a0001c0001t0002g0010others(61): Show | 64 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+1223C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21942096 | ||||||
| chrX:21942118
|
C | CA | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+1245_49+1246ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21942118 | ||||||
| chrX:21942170
|
T | TC | 1 | a0001c0001t0002g0005 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.49+1299dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942170 | |||||
| chrX:21942383
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+1510T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21942383 | ||||||
| chrX:21942416
|
G | GA | 4 | a0001c0001t0001g0006a0001c0001t0003g0110a0001c0001t0003g0111others(1): Show | 4 | HG02055.hp1 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1553dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942416 | |||||
| chrX:21942416
|
GAAA | G | 4 | a0001c0001t0002g0116a0001c0001t0002g0138a0001c0001t0002g0160others(1): Show | 4 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+1551_49+1553del others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942416 | |||||
| chrX:21942482
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.49+1609G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21942482 | ||||||
| chrX:21942582
|
A | AG | 1 | a0001c0001t0002g0005 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.49+1712dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942582 | |||||
| chrX:21942653
|
A | G | 2 | a0001c0001t0005g0266a0001c0001t0005g0283 | 2 | NA18955.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.49+1780A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21942653 | ||||||
| chrX:21942829
|
C | CT | 73 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0039others(70): Show | 74 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.49+1978dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942829 | |||||
| chrX:21942829
|
C | CTT | 5 | a0001c0001t0001g0079a0001c0001t0002g0137a0001c0001t0002g0287others(2): Show | 5 | HG02257.hp2 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+1977_49+1978dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942829 | |||||
| chrX:21942829
|
CT | C | 14 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0080others(11): Show | 14 | HG00597.hp2 HG01168.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+1978delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942829 | |||||
| chrX:21942829
|
CTTTTTTT | C | 1 | a0001c0001t0002g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.49+1972_49+1978del others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942829 | |||||
| chrX:21942851
|
T | TA | 1 | a0001c0001t0011g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+1980dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21942851 | |||||
| chrX:21942982
|
G | C | 1 | a0001c0001t0003g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+2109G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21942982 | ||||||
| chrX:21943002
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.49+2129G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943002 | ||||||
| chrX:21943006
|
AT | A | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+2141delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943006 | |||||
| chrX:21943044
|
A | AC | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+2173dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943044 | |||||
| chrX:21943053
|
GC | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+2182delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943053 | |||||
| chrX:21943090
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0004g0016 | 2 | HG02976.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.49+2217G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943090 | ||||||
| chrX:21943142
|
G | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0164others(2): Show | 5 | HG01106.hp1 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+2269G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943142 | ||||||
| chrX:21943203
|
ACT | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(63): Show | 66 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.49+2333_49+2334del others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943203 | |||||
| chrX:21943232
|
TC | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+2361delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943232 | |||||
| chrX:21943259
|
T | C | 1 | a0003c0006t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.49+2386T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943259 | ||||||
| chrX:21943284
|
GT | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+2416delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943284 | |||||
| chrX:21943308
|
GA | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+2439delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943308 | |||||
| chrX:21943327
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.49+2454A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943327 | ||||||
| chrX:21943349
|
T | TG | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+2480dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943349 | |||||
| chrX:21943524
|
AG | A | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+2654delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943524 | |||||
| chrX:21943631
|
G | A | 35 | a0001c0001t0002g0005a0001c0001t0002g0179a0001c0001t0002g0180others(32): Show | 35 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.49+2758G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943631 | ||||||
| chrX:21943634
|
T | TG | 1 | a0001c0001t0001g0297 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.49+2768dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21943634 | |||||
| chrX:21943656
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.49+2783A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943656 | ||||||
| chrX:21943675
|
C | T | 7 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0003g0008others(4): Show | 7 | HG02486.hp1 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+2802C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943675 | ||||||
| chrX:21943933
|
G | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0140a0001c0001t0004g0066others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+3060G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21943933 | ||||||
| chrX:21944002
|
C | CT | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3132dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944002 | |||||
| chrX:21944031
|
T | G | 8 | a0001c0001t0002g0007a0001c0001t0002g0010a0001c0001t0003g0008others(5): Show | 8 | HG02109.hp1 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+3158T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944031 | ||||||
| chrX:21944047
|
CT | C | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+3176delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944047 | |||||
| chrX:21944097
|
A | ACT | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3225_49+3226ins others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944097 | |||||
| chrX:21944102
|
AC | A | 1 | a0001c0001t0001g0297 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.49+3231delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944102 | |||||
| chrX:21944139
|
T | TG | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3268dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944139 | |||||
| chrX:21944155
|
C | CT | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3283dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944155 | |||||
| chrX:21944194
|
T | TA | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+3328dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944194 | |||||
| chrX:21944229
|
GA | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+3358delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944229 | |||||
| chrX:21944267
|
A | AT | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3398dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944267 | |||||
| chrX:21944333
|
C | T | 1 | a0001c0001t0006g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.49+3460C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944333 | ||||||
| chrX:21944342
|
T | TG | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3471dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944342 | |||||
| chrX:21944374
|
TGCTAGGC others(2): Show |
T | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+3503_49+3511del others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944374 | |||||
| chrX:21944398
|
C | CAG | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3530_49+3531dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944398 | |||||
| chrX:21944414
|
G | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(68): Show | 71 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.49+3541G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944414 | ||||||
| chrX:21944461
|
G | C | 1 | a0001c0001t0003g0268 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.49+3588G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944461 | ||||||
| chrX:21944522
|
C | CA | 9 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0044others(6): Show | 9 | HG00099.hp2 HG02683.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+3672dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
C | CAAAAA | 2 | a0001c0001t0002g0194a0001c0001t0002g0212 | 2 | HG00639.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.49+3668_49+3672dup others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
C | CAAAAAA | 26 | a0001c0001t0002g0179a0001c0001t0002g0182a0001c0001t0002g0183others(23): Show | 26 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.49+3667_49+3672dup others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
C | CAAAAAAA | 4 | a0001c0001t0002g0005a0001c0001t0002g0180a0001c0001t0002g0181others(1): Show | 4 | HG00597.hp2 HG02071.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+3666_49+3672dup others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
C | CAAAAAAA others(1): Show |
1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+3665_49+3672dup others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.49+3660_49+3672dup others(13): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0006g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.49+3658_49+3672dup others(15): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
CA | C | 60 | a0001c0001t0001g0037a0001c0001t0001g0061a0001c0001t0001g0100others(57): Show | 60 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.49+3672delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
CAA | C | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.49+3671_49+3672del others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
CAAAAA | C | 1 | a0001c0005t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49+3668_49+3672del others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
CAAAAAA | C | 25 | a0001c0001t0002g0267a0001c0001t0002g0276a0001c0001t0002g0277others(22): Show | 25 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.49+3667_49+3672del others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
CAAAAAAA | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0065a0001c0001t0004g0062others(3): Show | 6 | HG00741.hp2 HG01256.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+3666_49+3672del others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944522
|
CAAAAAAA others(1): Show |
C | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0229 | 3 | HG01952.hp1 HG01978.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.49+3665_49+3672del others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944522 | |||||
| chrX:21944539
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0004g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49+3672_49+3673ins others(26): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944539 | |||||
| chrX:21944539
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0004g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.49+3672_49+3673ins others(22): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944539 | |||||
| chrX:21944539
|
A | AAAAAAAA others(14): Show |
3 | a0001c0001t0004g0066a0001c0001t0004g0102a0001c0001t0006g0082 | 3 | HG01167.hp1 HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(21): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944539 | |||||
| chrX:21944539
|
A | AAAAAAAA others(13): Show |
5 | a0001c0001t0001g0072a0001c0001t0001g0105a0001c0001t0004g0067others(2): Show | 5 | HG00735.hp1 HG01169.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(20): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944539 | |||||
| chrX:21944539
|
A | AAAAAAAA others(12): Show |
7 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0140others(4): Show | 7 | HG00735.hp2 HG01516.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(19): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944539 | |||||
| chrX:21944539
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0004g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.49+3672_49+3673ins others(14): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944539 | |||||
| chrX:21944539
|
A | AAAAAG | 1 | a0001c0001t0011g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+3670_49+3671ins others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944539 | |||||
| chrX:21944541
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+3668A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944541 | ||||||
| chrX:21944544
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0231 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.49+3672_49+3673ins others(30): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAAA others(22): Show |
3 | a0001c0001t0001g0222a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG01261.hp1 NA18940.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(29): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0234a0003c0006t0001g0230 | 2 | HG00438.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(28): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAAA others(20): Show |
2 | a0001c0001t0001g0235a0001c0001t0004g0141 | 2 | HG02145.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(27): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAAA others(19): Show |
3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0223 | 3 | HG00597.hp1 HG02523.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(26): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAAA others(18): Show |
17 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0224others(14): Show | 17 | HG00639.hp1 HG00642.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(25): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0256 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.49+3672_49+3673ins others(19): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAAA others(17): Show |
18 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0001g0228others(15): Show | 18 | HG01168.hp2 HG02129.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(24): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAAA others(10): Show |
2 | a0001c0001t0001g0164a0001c0001t0004g0174 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.49+3672_49+3673ins others(17): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944544
|
A | AAAAAAGA others(4): Show |
1 | a0001c0001t0001g0227 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.49+3672_49+3673ins others(11): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944544 | |||||
| chrX:21944545
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.49+3672A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944545 | ||||||
| chrX:21944546
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.49+3673G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944546 | ||||||
| chrX:21944566
|
T | TGTG | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3694_49+3695ins others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944566 | |||||
| chrX:21944568
|
G | A | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3695G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944568 | ||||||
| chrX:21944569
|
T | G | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3696T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944569 | ||||||
| chrX:21944589
|
TC | T | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+3719delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944589 | |||||
| chrX:21944671
|
G | GA | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+3801dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944671 | |||||
| chrX:21944689
|
AAAC | A | 2 | a0001c0001t0002g0287a0001c0001t0002g0289 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.49+3819_49+3821del others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944689 | |||||
| chrX:21944694
|
A | AG | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+3824dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944694 | |||||
| chrX:21944767
|
C | T | 2 | a0001c0001t0005g0266a0001c0001t0005g0283 | 2 | NA18955.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.49+3894C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944767 | ||||||
| chrX:21944790
|
C | T | 1 | a0001c0001t0006g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.49+3917C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944790 | ||||||
| chrX:21944834
|
C | CG | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.49+3964dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944834 | |||||
| chrX:21944834
|
C | T | 2 | a0001c0001t0003g0265a0001c0001t0006g0014 | 2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.49+3961C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944834 | ||||||
| chrX:21944905
|
GGAGGTGG others(10): Show |
G | 2 | a0001c0001t0004g0109a0001c0001t0006g0082 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.49+4036_49+4052del others(17): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944905 | |||||
| chrX:21944919
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.49+4046C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21944919 | ||||||
| chrX:21944960
|
C | CA | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4088dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944960 | |||||
| chrX:21944997
|
C | CA | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.49+4129dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21944997 | |||||
| chrX:21945009
|
T | TA | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4136_49+4137ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945009 | ||||||
| chrX:21945025
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(196): Show | 199 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.49+4152A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945025 | ||||||
| chrX:21945184
|
G | GA | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4311_49+4312ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945184 | ||||||
| chrX:21945255
|
T | TC | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4384dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945255 | |||||
| chrX:21945414
|
T | G | 3 | a0001c0001t0004g0144a0001c0001t0006g0119a0001c0001t0011g0139 | 3 | HG02723.hp1 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.49+4541T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945414 | ||||||
| chrX:21945472
|
C | G | 3 | a0001c0001t0004g0144a0001c0001t0006g0119a0001c0001t0011g0139 | 3 | HG02723.hp1 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.49+4599C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945472 | ||||||
| chrX:21945492
|
G | GT | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4619_49+4620ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945492 | ||||||
| chrX:21945511
|
AC | A | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4641delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945511 | |||||
| chrX:21945577
|
A | G | 1 | a0001c0001t0004g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49+4704A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945577 | ||||||
| chrX:21945604
|
G | GT | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4732dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945604 | |||||
| chrX:21945612
|
G | GGT | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4739_49+4740ins others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945612 | ||||||
| chrX:21945613
|
T | A | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4740T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945613 | ||||||
| chrX:21945629
|
T | C | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4756T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945629 | ||||||
| chrX:21945630
|
C | T | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4757C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945630 | ||||||
| chrX:21945634
|
T | TC | 51 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0060others(48): Show | 51 | HG00609.hp1 HG01070.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.49+4771dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945634 | |||||
| chrX:21945634
|
T | TCC | 22 | a0001c0001t0001g0073a0001c0001t0001g0140a0001c0001t0002g0114others(19): Show | 22 | HG00735.hp1 HG00735.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.49+4770_49+4771dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945634 | |||||
| chrX:21945634
|
T | TCCC | 27 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0072others(24): Show | 27 | HG00597.hp1 HG01169.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+4769_49+4771dup others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945634 | |||||
| chrX:21945634
|
T | TCCCC | 27 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0075others(24): Show | 27 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+4768_49+4771dup others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945634 | |||||
| chrX:21945634
|
T | TCCCCC | 1 | a0001c0001t0001g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+4767_49+4771dup others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945634 | |||||
| chrX:21945634
|
TC | T | 2 | a0001c0001t0005g0261a0001c0001t0015g0004 | 2 | HG00673.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.49+4771delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945634 | |||||
| chrX:21945639
|
C | A | 7 | a0001c0001t0003g0259a0001c0001t0003g0260a0001c0001t0003g0265others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+4766C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945639 | ||||||
| chrX:21945639
|
CCCCCCA | C | 1 | a0001c0001t0002g0220 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.49+4772_49+4777del others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945639 | |||||
| chrX:21945648
|
C | A | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4775C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945648 | ||||||
| chrX:21945651
|
T | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(196): Show | 199 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.49+4778T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945651 | ||||||
| chrX:21945711
|
G | GC | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4840dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945711 | |||||
| chrX:21945714
|
TC | T | 1 | a0001c0001t0001g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.49+4844delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945714 | |||||
| chrX:21945766
|
A | AG | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4895dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945766 | |||||
| chrX:21945771
|
C | T | 7 | a0001c0001t0003g0259a0001c0001t0003g0260a0001c0001t0003g0265others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+4898C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945771 | ||||||
| chrX:21945795
|
T | G | 16 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(13): Show | 16 | HG00735.hp1 HG00735.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+4922T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21945795 | ||||||
| chrX:21945849
|
T | TC | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4978dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945849 | |||||
| chrX:21945866
|
A | AC | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+4996dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21945866 | |||||
| chrX:21946082
|
A | AT | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 111 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.49+5215dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21946082 | |||||
| chrX:21946148
|
GT | G | 1 | a0001c0001t0007g0026 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.49+5282delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21946148 | |||||
| chrX:21946241
|
A | AG | 1 | a0001c0001t0001g0245 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.49+5373dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21946241 | |||||
| chrX:21946243
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0084a0001c0001t0007g0026 | 4 | NA18964.hp2 NA18989.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+5370G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21946243 | ||||||
| chrX:21946263
|
G | A | 2 | a0001c0001t0004g0016a0001c0001t0004g0017 | 2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.49+5390G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21946263 | ||||||
| chrX:21946276
|
G | A | 54 | a0001c0001t0001g0145a0001c0001t0002g0112a0001c0001t0002g0114others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+5403G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21946276 | ||||||
| chrX:21946300
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.49+5427A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21946300 | ||||||
| chrX:21946415
|
C | A | 40 | a0001c0001t0002g0112a0001c0001t0002g0114a0001c0001t0002g0125others(37): Show | 40 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.49+5542C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21946415 | ||||||
| chrX:21946427
|
AT | A | 1 | a0001c0001t0001g0245 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.49+5558delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21946427 | |||||
| chrX:21946503
|
C | A | 36 | a0001c0001t0001g0040a0001c0001t0001g0085a0001c0001t0002g0005others(33): Show | 36 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.49+5630C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21946503 | ||||||
| chrX:21946756
|
C | A | 2 | a0001c0001t0005g0272a0001c0001t0005g0273 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.49+5883C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21946756 | ||||||
| chrX:21946914
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.49+6041C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21946914 | ||||||
| chrX:21947049
|
G | A | 37 | a0001c0001t0001g0040a0001c0001t0001g0085a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.49+6176G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947049 | ||||||
| chrX:21947152
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+6279A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947152 | ||||||
| chrX:21947283
|
A | G | 1 | a0001c0001t0004g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.49+6410A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947283 | ||||||
| chrX:21947456
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.49+6583T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947456 | ||||||
| chrX:21947467
|
AAAC | A | 3 | a0001c0001t0004g0142a0001c0001t0004g0163a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.49+6606_49+6608del others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21947467 | |||||
| chrX:21947512
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+6639C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947512 | ||||||
| chrX:21947725
|
C | G | 4 | a0001c0001t0001g0145a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 4 | HG01070.hp2 HG02109.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+6852C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947725 | ||||||
| chrX:21947819
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49+6946G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947819 | ||||||
| chrX:21947867
|
GAGA | G | 9 | a0001c0001t0003g0133a0001c0001t0003g0259a0001c0001t0003g0260others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+6998_49+7000del others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21947867 | |||||
| chrX:21947879
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.49+7006T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947879 | ||||||
| chrX:21947903
|
CATGCG | C | 1 | a0001c0001t0003g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.49+7031_49+7035del others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21947903 | ||||||
| chrX:21947917
|
G | GT | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+7047dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21947917 | |||||
| chrX:21948002
|
T | TC | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+7129_49+7130ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21948002 | ||||||
| chrX:21948137
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0023 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.49+7264C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21948137 | ||||||
| chrX:21948439
|
C | CT | 2 | a0001c0001t0003g0285a0001c0001t0006g0083 | 2 | HG00099.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.49+7583dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
C | CTTTTT | 7 | a0001c0001t0002g0007a0001c0001t0002g0151a0001c0001t0002g0289others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+7579_49+7583dup others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
C | CTTTTTT | 54 | a0001c0001t0002g0112a0001c0001t0002g0114a0001c0001t0002g0125others(51): Show | 54 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.49+7578_49+7583dup others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
C | CTTTTTTT others(3): Show |
9 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0076others(6): Show | 9 | HG01106.hp1 HG01169.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+7574_49+7583dup others(10): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
C | CTTTTTTT others(4): Show |
13 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0140others(10): Show | 13 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.49+7573_49+7583dup others(11): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
C | CTTTTTTT others(5): Show |
14 | a0001c0001t0002g0123a0001c0001t0002g0130a0001c0001t0002g0131others(11): Show | 14 | HG00597.hp2 HG01081.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+7572_49+7583dup others(12): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
C | CTTTTTTT others(6): Show |
24 | a0001c0001t0001g0040a0001c0001t0001g0085a0001c0001t0002g0005others(21): Show | 24 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.49+7571_49+7583dup others(13): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
C | CTTTTTTT others(7): Show |
11 | a0001c0001t0002g0179a0001c0001t0002g0184a0001c0001t0002g0186others(8): Show | 11 | HG00558.hp2 HG01943.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+7570_49+7583dup others(14): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+7569_49+7583dup others(15): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
CT | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG00280.hp1 HG02698.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+7583delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
CTTTTT | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(61): Show | 64 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+7579_49+7583del others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948439
|
CTTTTTT | C | 1 | a0001c0001t0001g0223 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.49+7578_49+7583del others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948439 | |||||
| chrX:21948467
|
C | CT | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+7598dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948467 | |||||
| chrX:21948503
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+7630A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21948503 | ||||||
| chrX:21948512
|
TC | T | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+7643delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948512 | |||||
| chrX:21948586
|
A | G | 2 | a0001c0001t0005g0266a0001c0001t0005g0283 | 2 | NA18955.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.49+7713A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21948586 | ||||||
| chrX:21948598
|
C | T | 1 | a0001c0001t0005g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.49+7725C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21948598 | ||||||
| chrX:21948665
|
G | C | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+7792G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21948665 | ||||||
| chrX:21948690
|
A | AC | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+7819dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948690 | |||||
| chrX:21948750
|
T | TA | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.49+7882dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948750 | |||||
| chrX:21948863
|
C | A | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+7990C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21948863 | ||||||
| chrX:21948894
|
CT | C | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+8025delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948894 | |||||
| chrX:21948986
|
A | AC | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+8114dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21948986 | |||||
| chrX:21949011
|
A | G | 1 | a0001c0001t0002g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.49+8138A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949011 | ||||||
| chrX:21949072
|
TC | T | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+8201delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21949072 | |||||
| chrX:21949073
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.49+8200C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949073 | ||||||
| chrX:21949229
|
TC | T | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.49+8359delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21949229 | |||||
| chrX:21949439
|
C | T | 50 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(47): Show | 50 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.49+8566C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949439 | ||||||
| chrX:21949456
|
A | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.49+8583A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949456 | ||||||
| chrX:21949505
|
T | A | 4 | a0001c0001t0002g0123a0001c0001t0004g0043a0001c0001t0006g0082others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+8632T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949505 | ||||||
| chrX:21949506
|
A | G | 1 | a0001c0001t0006g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.49+8633A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949506 | ||||||
| chrX:21949535
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0012g0048 | 2 | HG02273.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.49+8662G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949535 | ||||||
| chrX:21949580
|
T | G | 1 | a0001c0005t0001g0219 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49+8707T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949580 | ||||||
| chrX:21949663
|
G | A | 3 | a0001c0001t0004g0118a0001c0001t0004g0141a0001c0001t0004g0143 | 3 | HG02145.hp1 HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+8790G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949663 | ||||||
| chrX:21949817
|
G | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+8944G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21949817 | ||||||
| chrX:21949950
|
G | GA | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG00741.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.49+9090dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21949950 | |||||
| chrX:21949950
|
GA | G | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.49+9090delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21949950 | |||||
| chrX:21949950
|
GAA | G | 1 | a0001c0001t0005g0264 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.49+9089_49+9090del others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21949950 | |||||
| chrX:21950094
|
G | A | 9 | a0001c0001t0003g0133a0001c0001t0003g0259a0001c0001t0003g0260others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+9221G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950094 | ||||||
| chrX:21950159
|
T | C | 71 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(68): Show | 71 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.49+9286T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950159 | ||||||
| chrX:21950433
|
C | CT | 5 | a0001c0001t0001g0024a0001c0001t0001g0108a0001c0001t0001g0162others(2): Show | 5 | HG00741.hp2 HG02486.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+9581dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21950433 | |||||
| chrX:21950433
|
CT | C | 34 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.49+9581delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21950433 | |||||
| chrX:21950433
|
CTT | C | 99 | a0001c0001t0001g0040a0001c0001t0001g0085a0001c0001t0002g0005others(96): Show | 99 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.49+9580_49+9581del others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21950433 | |||||
| chrX:21950433
|
CTTT | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.49+9579_49+9581del others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21950433 | |||||
| chrX:21950433
|
CTTTT | C | 3 | a0001c0001t0001g0228a0001c0001t0002g0138a0001c0001t0007g0239 | 3 | HG00323.hp1 HG01168.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.49+9578_49+9581del others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21950433 | |||||
| chrX:21950452
|
T | G | 1 | a0001c0001t0003g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49+9579T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950452 | ||||||
| chrX:21950603
|
C | G | 1 | a0001c0001t0003g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+9730C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950603 | ||||||
| chrX:21950608
|
C | T | 3 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0120 | 3 | HG02055.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+9735C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950608 | ||||||
| chrX:21950647
|
T | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+9774T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950647 | ||||||
| chrX:21950665
|
G | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+9792G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950665 | ||||||
| chrX:21950666
|
G | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+9793G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950666 | ||||||
| chrX:21950726
|
C | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+9853C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950726 | ||||||
| chrX:21950742
|
C | T | 2 | a0001c0001t0003g0159a0001c0001t0004g0028 | 2 | HG01081.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.49+9869C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950742 | ||||||
| chrX:21950808
|
G | A | 4 | a0001c0001t0002g0198a0001c0001t0002g0205a0001c0001t0002g0206others(1): Show | 4 | HG00558.hp2 NA18990.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+9935G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950808 | ||||||
| chrX:21950908
|
G | A | 1 | a0001c0001t0003g0271 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.49+10035G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950908 | ||||||
| chrX:21950931
|
A | G | 1 | a0001c0001t0003g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.49+10058A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950931 | ||||||
| chrX:21950970
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.49+10097A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950970 | ||||||
| chrX:21950993
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.49+10120C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21950993 | ||||||
| chrX:21951072
|
A | G | 1 | a0001c0001t0005g0264 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.49+10199A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21951072 | ||||||
| chrX:21951150
|
C | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+10277C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21951150 | ||||||
| chrX:21951435
|
A | G | 3 | a0001c0001t0004g0142a0001c0001t0004g0163a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.49+10562A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21951435 | ||||||
| chrX:21951521
|
A | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+10648A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21951521 | ||||||
| chrX:21951736
|
C | CT | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.49+10876dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21951736 | |||||
| chrX:21951736
|
C | CTT | 1 | a0001c0001t0002g0204 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10875_49+10876d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21951736 | |||||
| chrX:21951736
|
CT | C | 3 | a0001c0001t0001g0087a0001c0001t0003g0115a0001c0001t0011g0139 | 3 | HG02723.hp1 HG02735.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.49+10876delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21951736 | |||||
| chrX:21951950
|
C | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.49+11077C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21951950 | ||||||
| chrX:21952406
|
GTTGT | G | 95 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(92): Show | 95 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.49+11548_49+11551d others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952406 | |||||
| chrX:21952406
|
GTTGTTTG others(1): Show |
G | 1 | a0001c0001t0002g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+11544_49+11551d others(10): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952406 | |||||
| chrX:21952412
|
TGTTTG | T | 1 | a0001c0001t0001g0145 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.49+11540_49+11544d others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952412 | ||||||
| chrX:21952415
|
TTG | T | 1 | a0001c0001t0002g0191 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.49+11544_49+11545d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952415 | |||||
| chrX:21952416
|
TGTTTG | T | 9 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0164others(6): Show | 9 | HG01081.hp1 HG01081.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+11544_49+11548d others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952416 | ||||||
| chrX:21952417
|
GTTTGT | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.49+11548_49+11552d others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952417 | |||||
| chrX:21952417
|
GTTTGTT | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | HG01943.hp1 NA18940.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+11548_49+11553d others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952417 | |||||
| chrX:21952421
|
G | GT | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.49+11563dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952421 | |||||
| chrX:21952421
|
G | T | 22 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(19): Show | 22 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.49+11548G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952421 | ||||||
| chrX:21952421
|
GT | G | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.49+11563delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952421 | |||||
| chrX:21952425
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0297 | 2 | HG02683.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.49+11552T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952425 | ||||||
| chrX:21952440
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.49+11567T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952440 | ||||||
| chrX:21952571
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+11698A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952571 | ||||||
| chrX:21952608
|
G | GT | 1 | a0001c0001t0001g0222 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.49+11736dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952608 | |||||
| chrX:21952749
|
GT | G | 5 | a0001c0001t0002g0123a0001c0001t0003g0271a0001c0001t0004g0043others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+11884delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952749 | |||||
| chrX:21952860
|
A | AC | 1 | a0001c0001t0007g0286 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.49+11993dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21952860 | |||||
| chrX:21952910
|
C | T | 31 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(28): Show | 31 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.49+12037C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952910 | ||||||
| chrX:21952933
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.49+12060C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952933 | ||||||
| chrX:21952946
|
A | G | 37 | a0001c0001t0001g0040a0001c0001t0001g0085a0001c0001t0002g0005others(34): Show | 37 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.49+12073A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952946 | ||||||
| chrX:21952973
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.49+12100G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21952973 | ||||||
| chrX:21953009
|
C | T | 4 | a0001c0001t0002g0007a0001c0001t0003g0012a0001c0001t0003g0115others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+12136C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953009 | ||||||
| chrX:21953316
|
G | C | 1 | a0001c0001t0002g0208 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.49+12443G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953316 | ||||||
| chrX:21953359
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.49+12486G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953359 | ||||||
| chrX:21953464
|
G | A | 1 | a0001c0001t0003g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.49+12591G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953464 | ||||||
| chrX:21953571
|
C | T | 31 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(28): Show | 31 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.49+12698C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953571 | ||||||
| chrX:21953595
|
G | GT | 1 | a0001c0002t0003g0169 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.49+12725dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21953595 | |||||
| chrX:21953662
|
TG | T | 1 | a0001c0001t0007g0239 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.49+12790delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953662 | ||||||
| chrX:21953664
|
C | T | 1 | a0001c0001t0007g0239 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.49+12791C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953664 | ||||||
| chrX:21953667
|
C | T | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49+12794C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953667 | ||||||
| chrX:21953692
|
T | G | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.49+12819T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21953692 | ||||||
| chrX:21953890
|
A | AT | 99 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(96): Show | 100 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.49+13032dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21953890 | |||||
| chrX:21953890
|
A | ATT | 5 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0098others(2): Show | 5 | HG00423.hp2 HG04204.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13031_49+13032d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21953890 | |||||
| chrX:21953890
|
AT | A | 31 | a0001c0001t0002g0267a0001c0001t0002g0276a0001c0001t0002g0277others(28): Show | 31 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.49+13032delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21953890 | |||||
| chrX:21953890
|
ATT | A | 47 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(44): Show | 47 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.49+13031_49+13032d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21953890 | |||||
| chrX:21953890
|
ATTT | A | 29 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(26): Show | 29 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.49+13030_49+13032d others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21953890 | |||||
| chrX:21953963
|
C | CTAG | 28 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(25): Show | 28 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.49+13092_49+13094d others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21953963 | |||||
| chrX:21953963
|
C | CTCG | 3 | a0001c0001t0004g0142a0001c0001t0004g0163a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.49+13091_49+13092i others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21953963 | |||||
| chrX:21954036
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(124): Show | 128 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.50-13160A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954036 | ||||||
| chrX:21954069
|
G | A | 1 | a0003c0006t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.50-13127G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954069 | ||||||
| chrX:21954089
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.50-13107G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954089 | ||||||
| chrX:21954168
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.50-13028A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954168 | ||||||
| chrX:21954224
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.50-12972C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954224 | ||||||
| chrX:21954304
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0002g0212 | 2 | HG00639.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.50-12892G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954304 | ||||||
| chrX:21954336
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(124): Show | 128 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.50-12860T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954336 | ||||||
| chrX:21954402
|
A | G | 4 | a0001c0001t0002g0155a0001c0001t0002g0287a0001c0001t0002g0289others(1): Show | 4 | HG02723.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-12794A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954402 | ||||||
| chrX:21954417
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0009g0047 | 2 | NA18962.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.50-12779C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954417 | ||||||
| chrX:21954613
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.50-12583T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954613 | ||||||
| chrX:21954615
|
G | A | 31 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(28): Show | 31 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.50-12581G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954615 | ||||||
| chrX:21954690
|
C | T | 30 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0075others(27): Show | 30 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-12506C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954690 | ||||||
| chrX:21954709
|
T | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(124): Show | 128 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.50-12487T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954709 | ||||||
| chrX:21954730
|
TA | T | 4 | a0001c0001t0002g0007a0001c0001t0003g0012a0001c0001t0003g0115others(1): Show | 4 | HG02109.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-12465delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954730 | ||||||
| chrX:21954897
|
C | T | 1 | a0001c0001t0003g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-12299C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21954897 | ||||||
| chrX:21955025
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0002g0184 | 2 | NA18960.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.50-12171G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955025 | ||||||
| chrX:21955128
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.50-12068G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955128 | ||||||
| chrX:21955161
|
G | A | 34 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(31): Show | 34 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.50-12035G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955161 | ||||||
| chrX:21955285
|
A | G | 6 | a0001c0001t0003g0133a0001c0001t0003g0259a0001c0001t0003g0260others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-11911A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955285 | ||||||
| chrX:21955427
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.50-11769T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955427 | ||||||
| chrX:21955525
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-11671C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955525 | ||||||
| chrX:21955678
|
C | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.50-11518C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955678 | ||||||
| chrX:21955731
|
C | T | 4 | a0001c0001t0001g0140a0001c0001t0004g0062a0001c0001t0004g0063others(1): Show | 4 | HG00735.hp2 HG01256.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-11465C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955731 | ||||||
| chrX:21955765
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.50-11431C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955765 | ||||||
| chrX:21955923
|
G | T | 1 | a0001c0001t0002g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.50-11273G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955923 | ||||||
| chrX:21955999
|
A | C | 1 | a0001c0001t0001g0002 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.50-11197A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21955999 | ||||||
| chrX:21956189
|
G | A | 1 | a0001c0001t0005g0275 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.50-11007G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21956189 | ||||||
| chrX:21956303
|
G | A | 52 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(49): Show | 52 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.50-10893G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21956303 | ||||||
| chrX:21956427
|
G | A | 53 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(50): Show | 53 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.50-10769G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21956427 | ||||||
| chrX:21956454
|
T | A | 46 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0044others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.50-10742T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21956454 | ||||||
| chrX:21956459
|
T | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0106 | 2 | NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.50-10737T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21956459 | ||||||
| chrX:21956484
|
T | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.50-10712T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21956484 | ||||||
| chrX:21956531
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.50-10665G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21956531 | ||||||
| chrX:21956619
|
G | GC | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-10575dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21956619 | |||||
| chrX:21956763
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.50-10433C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21956763 | ||||||
| chrX:21957008
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.50-10188G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957008 | ||||||
| chrX:21957042
|
T | TG | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-10150dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21957042 | |||||
| chrX:21957064
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0002g0130a0001c0001t0002g0131others(1): Show | 4 | HG01070.hp2 HG02109.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-10132C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957064 | ||||||
| chrX:21957153
|
C | CT | 17 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0049others(14): Show | 17 | HG00558.hp2 HG02083.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.50-10026dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21957153 | |||||
| chrX:21957153
|
CT | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.50-10026delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21957153 | |||||
| chrX:21957153
|
CTT | C | 1 | a0001c0001t0001g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.50-10027_50-10026d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21957153 | |||||
| chrX:21957219
|
A | G | 2 | a0001c0001t0004g0142a0001c0001t0004g0163 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9977A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957219 | ||||||
| chrX:21957310
|
AT | A | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-9882delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21957310 | |||||
| chrX:21957329
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0164others(1): Show | 4 | HG01106.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-9867T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957329 | ||||||
| chrX:21957368
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(157): Show | 160 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.50-9828C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957368 | ||||||
| chrX:21957401
|
A | G | 5 | a0001c0001t0003g0271a0001c0001t0003g0285a0001c0001t0004g0043others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-9795A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957401 | ||||||
| chrX:21957423
|
A | G | 5 | a0001c0001t0003g0133a0001c0001t0003g0259a0001c0001t0003g0260others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-9773A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957423 | ||||||
| chrX:21957473
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(162): Show | 165 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.50-9723G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957473 | ||||||
| chrX:21957496
|
C | T | 1 | a0001c0001t0006g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-9700C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21957496 | ||||||
| chrX:21957959
|
G | GT | 4 | a0001c0001t0001g0002a0001c0001t0004g0074a0001c0001t0007g0226others(1): Show | 4 | HG02886.hp2 NA19078.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-9223dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21957959 | |||||
| chrX:21957959
|
GT | G | 46 | a0001c0001t0001g0117a0001c0001t0002g0112a0001c0001t0002g0114others(43): Show | 46 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.50-9223delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21957959 | |||||
| chrX:21958251
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.50-8945T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21958251 | ||||||
| chrX:21958290
|
T | C | 1 | a0001c0001t0004g0104 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.50-8906T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21958290 | ||||||
| chrX:21958477
|
A | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0164others(1): Show | 4 | HG01106.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-8719A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21958477 | ||||||
| chrX:21958525
|
G | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(201): Show | 204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.50-8671G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21958525 | ||||||
| chrX:21958530
|
C | T | 1 | a0001c0001t0004g0174 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.50-8666C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21958530 | ||||||
| chrX:21958584
|
C | G | 4 | a0001c0001t0003g0121a0001c0001t0004g0142a0001c0001t0004g0163others(1): Show | 4 | HG02809.hp1 HG02922.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-8612C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21958584 | ||||||
| chrX:21958738
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-8458G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21958738 | ||||||
| chrX:21958845
|
G | T | 1 | a0001c0001t0004g0174 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.50-8351G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21958845 | ||||||
| chrX:21959064
|
C | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(104): Show | 107 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.50-8132C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21959064 | ||||||
| chrX:21959089
|
T | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.50-8107T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21959089 | ||||||
| chrX:21959406
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.50-7790G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21959406 | ||||||
| chrX:21959586
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.50-7610T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21959586 | ||||||
| chrX:21959658
|
G | C | 2 | a0001c0001t0004g0142a0001c0001t0004g0163 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.50-7538G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21959658 | ||||||
| chrX:21959889
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-7307A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21959889 | ||||||
| chrX:21959942
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(84): Show | 87 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.50-7254G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21959942 | ||||||
| chrX:21960035
|
CCG | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(159): Show | 162 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.50-7160_50-7159del others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960035 | ||||||
| chrX:21960104
|
C | T | 3 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0120 | 3 | HG02055.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.50-7092C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960104 | ||||||
| chrX:21960308
|
C | T | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0110others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-6888C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960308 | ||||||
| chrX:21960356
|
C | A | 2 | a0001c0001t0003g0157a0001c0001t0003g0158 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.50-6840C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960356 | ||||||
| chrX:21960399
|
CT | C | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.50-6786delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21960399 | |||||
| chrX:21960465
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0002g0212 | 2 | HG00639.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.50-6731G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960465 | ||||||
| chrX:21960488
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0110others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-6708A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960488 | ||||||
| chrX:21960611
|
C | T | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0110others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-6585C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960611 | ||||||
| chrX:21960709
|
C | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(159): Show | 162 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.50-6487C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960709 | ||||||
| chrX:21960713
|
AAGGCTCT others(1): Show |
A | 1 | a0001c0001t0005g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.50-6482_50-6475del others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960713 | ||||||
| chrX:21960880
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.50-6316A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21960880 | ||||||
| chrX:21961034
|
C | CT | 22 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0061others(19): Show | 22 | HG00408.hp2 HG01361.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.50-6137dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961034 | |||||
| chrX:21961034
|
C | CTT | 2 | a0001c0001t0001g0057a0001c0001t0002g0183 | 2 | NA19011.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.50-6138_50-6137dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961034 | |||||
| chrX:21961034
|
CT | C | 83 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0070others(80): Show | 83 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.50-6137delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961034 | |||||
| chrX:21961034
|
CTT | C | 6 | a0001c0001t0002g0112a0001c0001t0003g0012a0001c0001t0003g0115others(3): Show | 6 | HG01496.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-6138_50-6137del others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961034 | |||||
| chrX:21961034
|
CTTT | C | 30 | a0001c0001t0002g0114a0001c0001t0002g0123a0001c0001t0002g0126others(27): Show | 30 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-6139_50-6137del others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961034 | |||||
| chrX:21961034
|
CTTTT | C | 1 | a0001c0001t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.50-6140_50-6137del others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961034 | |||||
| chrX:21961098
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.50-6098C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21961098 | ||||||
| chrX:21961220
|
G | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(7): Show | 11 | HG01891.hp1 HG03491.hp2 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-5976G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21961220 | ||||||
| chrX:21961319
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.50-5877T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21961319 | ||||||
| chrX:21961545
|
C | T | 8 | a0001c0001t0001g0033a0001c0001t0001g0049a0001c0001t0001g0056others(5): Show | 8 | HG02083.hp1 NA18942.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-5651C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21961545 | ||||||
| chrX:21961589
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0012g0048 | 2 | HG02273.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.50-5607G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21961589 | ||||||
| chrX:21961607
|
C | CT | 5 | a0001c0001t0002g0007a0001c0001t0003g0012a0001c0001t0003g0115others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-5581dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961607 | |||||
| chrX:21961615
|
T | TC | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0110others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-5578dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961615 | |||||
| chrX:21961714
|
C | CA | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-5481dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961714 | |||||
| chrX:21961756
|
A | AG | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-5438dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961756 | |||||
| chrX:21961867
|
A | C | 1 | a0001c0001t0003g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.50-5329A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21961867 | ||||||
| chrX:21961927
|
C | CA | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-5266dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21961927 | |||||
| chrX:21961944
|
C | G | 1 | a0001c0001t0002g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.50-5252C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21961944 | ||||||
| chrX:21962009
|
T | C | 1 | a0001c0001t0004g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.50-5187T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962009 | ||||||
| chrX:21962042
|
T | C | 3 | a0001c0001t0002g0123a0001c0001t0002g0151a0001c0001t0003g0265 | 3 | HG01109.hp1 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.50-5154T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962042 | ||||||
| chrX:21962082
|
C | G | 1 | a0001c0001t0002g0138 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.50-5114C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962082 | ||||||
| chrX:21962199
|
T | TC | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-4997_50-4996ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962199 | ||||||
| chrX:21962248
|
A | G | 64 | a0001c0001t0002g0112a0001c0001t0002g0114a0001c0001t0002g0123others(61): Show | 64 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.50-4948A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962248 | ||||||
| chrX:21962347
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.50-4849G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962347 | ||||||
| chrX:21962377
|
A | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.50-4819A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962377 | ||||||
| chrX:21962836
|
G | C | 1 | a0001c0001t0011g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.50-4360G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962836 | ||||||
| chrX:21962857
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG02165.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.50-4339G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962857 | ||||||
| chrX:21962988
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.50-4208G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21962988 | ||||||
| chrX:21963092
|
AT | A | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-4102delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21963092 | |||||
| chrX:21963169
|
T | G | 3 | a0001c0001t0003g0012a0001c0001t0003g0115a0001c0001t0005g0013 | 3 | HG02109.hp1 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.50-4027T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963169 | ||||||
| chrX:21963250
|
G | T | 1 | a0001c0001t0006g0086 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.50-3946G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963250 | ||||||
| chrX:21963279
|
A | G | 1 | a0001c0002t0003g0169 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.50-3917A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963279 | ||||||
| chrX:21963464
|
A | AC | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-3732_50-3731ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963464 | ||||||
| chrX:21963587
|
A | T | 1 | a0001c0001t0002g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.50-3609A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963587 | ||||||
| chrX:21963588
|
G | T | 1 | a0001c0001t0006g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.50-3608G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963588 | ||||||
| chrX:21963623
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.50-3573G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963623 | ||||||
| chrX:21963778
|
C | T | 1 | a0001c0001t0005g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.50-3418C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963778 | ||||||
| chrX:21963904
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 77 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.50-3292G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21963904 | ||||||
| chrX:21964021
|
A | G | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.50-3175A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21964021 | ||||||
| chrX:21964062
|
A | AT | 72 | a0001c0001t0001g0173a0001c0001t0001g0284a0001c0001t0001g0297others(69): Show | 72 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.50-3117dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21964062 | |||||
| chrX:21964062
|
A | ATT | 2 | a0001c0001t0003g0175a0001c0001t0004g0017 | 2 | HG02738.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.50-3118_50-3117dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21964062 | |||||
| chrX:21964062
|
AT | A | 26 | a0001c0001t0001g0039a0001c0001t0001g0057a0001c0001t0001g0140others(23): Show | 26 | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.50-3117delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21964062 | |||||
| chrX:21964110
|
G | C | 2 | a0001c0001t0003g0124a0001c0001t0003g0152 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.50-3086G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21964110 | ||||||
| chrX:21964150
|
G | GA | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-3043dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21964150 | |||||
| chrX:21964556
|
TC | T | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-2637delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21964556 | |||||
| chrX:21964701
|
G | GT | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-2491dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21964701 | |||||
| chrX:21964823
|
T | C | 9 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0012others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.50-2373T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21964823 | ||||||
| chrX:21964936
|
GC | G | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-2257delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21964936 | |||||
| chrX:21964960
|
AG | A | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-2232delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21964960 | |||||
| chrX:21965022
|
A | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0184 | 2 | NA18960.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.50-2174A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21965022 | ||||||
| chrX:21965078
|
T | TC | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-2117dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965078 | |||||
| chrX:21965329
|
T | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.50-1867T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21965329 | ||||||
| chrX:21965364
|
C | T | 1 | a0001c0001t0006g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-1832C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21965364 | ||||||
| chrX:21965423
|
G | A | 33 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(30): Show | 33 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.50-1773G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21965423 | ||||||
| chrX:21965501
|
TG | T | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-1692delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965501 | |||||
| chrX:21965516
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.50-1680G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21965516 | ||||||
| chrX:21965584
|
C | CA | 120 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(117): Show | 121 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.50-1595dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965584 | |||||
| chrX:21965584
|
C | CAA | 6 | a0001c0001t0001g0018a0001c0001t0001g0061a0001c0001t0001g0173others(3): Show | 6 | HG02602.hp1 HG03239.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-1596_50-1595dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965584 | |||||
| chrX:21965584
|
C | CAAA | 1 | a0001c0001t0002g0190 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.50-1597_50-1595dup others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965584 | |||||
| chrX:21965584
|
C | CAAAAAA | 8 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0164others(5): Show | 8 | HG01106.hp1 HG02965.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-1600_50-1595dup others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965584 | |||||
| chrX:21965584
|
C | CAAAAAAA | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.50-1601_50-1595dup others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965584 | |||||
| chrX:21965584
|
C | CAAAAAAA others(1): Show |
57 | a0001c0001t0001g0035a0001c0001t0001g0140a0001c0001t0001g0224others(54): Show | 57 | HG00423.hp1 HG00597.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.50-1602_50-1595dup others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965584 | |||||
| chrX:21965584
|
C | CAAAAAAA others(2): Show |
10 | a0001c0001t0002g0126a0001c0001t0002g0137a0001c0001t0003g0008others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.50-1603_50-1595dup others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965584 | |||||
| chrX:21965584
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0003g0128a0001c0001t0003g0165 | 2 | HG00741.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.50-1604_50-1595dup others(10): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965584 | |||||
| chrX:21965604
|
C | T | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.50-1592C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21965604 | ||||||
| chrX:21965662
|
G | C | 9 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0012others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.50-1534G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21965662 | ||||||
| chrX:21965738
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.50-1458A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21965738 | ||||||
| chrX:21965747
|
C | CAAAAT | 1 | a0001c0001t0002g0155 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-1426_50-1422dup others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965747 | |||||
| chrX:21965783
|
T | TA | 1 | a0001c0001t0004g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.50-1404dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965783 | |||||
| chrX:21965783
|
TA | T | 1 | a0001c0001t0003g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.50-1404delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965783 | |||||
| chrX:21965962
|
TA | T | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-1227delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21965962 | |||||
| chrX:21966091
|
A | G | 1 | a0001c0001t0005g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.50-1105A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966091 | ||||||
| chrX:21966117
|
G | T | 33 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(30): Show | 33 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.50-1079G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966117 | ||||||
| chrX:21966123
|
G | A | 1 | a0001c0001t0005g0013 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.50-1073G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966123 | ||||||
| chrX:21966133
|
T | TAC | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-1062_50-1061dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21966133 | |||||
| chrX:21966144
|
TG | T | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-1050delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21966144 | |||||
| chrX:21966212
|
CT | C | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.50-980delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21966212 | |||||
| chrX:21966258
|
T | TC | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-934dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21966258 | |||||
| chrX:21966260
|
C | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.50-936C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966260 | ||||||
| chrX:21966402
|
C | G | 39 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(36): Show | 39 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-794C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966402 | ||||||
| chrX:21966459
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.50-737T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966459 | ||||||
| chrX:21966461
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.50-735C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966461 | ||||||
| chrX:21966514
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0094a0001c0001t0001g0257 | 3 | HG00323.hp2 HG01981.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.50-682C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966514 | ||||||
| chrX:21966568
|
T | TG | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-624dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21966568 | |||||
| chrX:21966709
|
G | GA | 1 | a0001c0001t0002g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.50-479dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21966709 | |||||
| chrX:21966875
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.50-321G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966875 | ||||||
| chrX:21966877
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.50-319T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21966877 | ||||||
| chrX:21967056
|
T | TTTTA | 30 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0001t0001g0045others(27): Show | 30 | HG00099.hp1 HG00639.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.50-107_50-104dupTT others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967056 | |||||
| chrX:21967056
|
T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0070a0001c0001t0001g0164a0001c0001t0002g0010others(1): Show | 4 | HG03486.hp2 NA18943.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-111_50-104dupTT others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967056 | |||||
| chrX:21967056
|
TTTTA | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0042others(5): Show | 8 | HG02155.hp1 HG02523.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-107_50-104delTT others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967056 | |||||
| chrX:21967056
|
TTTTATTT others(1): Show |
T | 3 | a0001c0001t0001g0088a0001c0001t0002g0160a0001c0001t0002g0161 | 3 | HG00280.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.50-111_50-104delTT others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967056 | |||||
| chrX:21967073
|
TTTATTTA others(13): Show |
T | 31 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(28): Show | 31 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.50-108_50-89delATT others(17): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967073 | |||||
| chrX:21967077
|
TTTATTTA others(9): Show |
T | 1 | a0001c0001t0003g0154 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.50-104_50-89delACT others(13): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967077 | |||||
| chrX:21967081
|
TTTATTTA others(5): Show |
T | 2 | a0001c0001t0001g0247a0001c0001t0002g0180 | 2 | HG00597.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.50-103_50-92delCTT others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967081 | |||||
| chrX:21967085
|
TTTATTTA others(1): Show |
T | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.50-103_50-96delCTT others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967085 | |||||
| chrX:21967089
|
TTTAC | T | 27 | a0001c0001t0001g0228a0001c0001t0001g0241a0001c0001t0001g0256others(24): Show | 27 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.50-103_50-100delCT others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 21967089 | |||||
| chrX:21967093
|
C | T | 6 | a0001c0001t0003g0121a0001c0001t0005g0274a0001c0001t0006g0014others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-103C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | chrX | 21967093 | ||||||
| chrX:21967346
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.170+30C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21967346 | ||||||
| chrX:21967399
|
C | G | 1 | a0001c0001t0002g0211 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.170+83C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21967399 | ||||||
| chrX:21967425
|
C | A | 35 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0070others(32): Show | 35 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.170+109C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21967425 | ||||||
| chrX:21967576
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.170+260G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21967576 | ||||||
| chrX:21967618
|
A | C | 50 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(47): Show | 50 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.170+302A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21967618 | ||||||
| chrX:21967823
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | NA18942.hp2 NA18966.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.170+507C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21967823 | ||||||
| chrX:21967846
|
C | T | 49 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(46): Show | 49 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.170+530C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21967846 | ||||||
| chrX:21967968
|
C | T | 31 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(28): Show | 31 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.170+652C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21967968 | ||||||
| chrX:21968206
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0105 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.170+890G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21968206 | ||||||
| chrX:21968289
|
G | C | 41 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(38): Show | 41 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.170+973G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21968289 | ||||||
| chrX:21968491
|
T | A | 1 | a0001c0001t0002g0220 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.170+1175T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21968491 | ||||||
| chrX:21968555
|
CG | C | 1 | a0001c0001t0001g0245 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.170+1244delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21968555 | |||||
| chrX:21968617
|
A | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0164others(1): Show | 4 | HG01106.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+1301A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21968617 | ||||||
| chrX:21968770
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.170+1454G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21968770 | ||||||
| chrX:21968969
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0164others(1): Show | 4 | HG01106.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+1653G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21968969 | ||||||
| chrX:21968987
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.170+1671A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21968987 | ||||||
| chrX:21969177
|
AC | A | 1 | a0001c0001t0001g0049 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.170+1865delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21969177 | |||||
| chrX:21969502
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.170+2186G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21969502 | ||||||
| chrX:21969543
|
G | A | 1 | a0001c0001t0005g0275 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.170+2227G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21969543 | ||||||
| chrX:21969830
|
T | C | 1 | a0001c0001t0004g0062 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.171-2067T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21969830 | ||||||
| chrX:21969965
|
C | T | 84 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.171-1932C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21969965 | ||||||
| chrX:21970075
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.171-1822G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21970075 | ||||||
| chrX:21970123
|
TA | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-1772delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970123 | |||||
| chrX:21970390
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0094a0001c0001t0001g0257 | 3 | HG00323.hp2 HG01981.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.171-1507G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21970390 | ||||||
| chrX:21970600
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.171-1297A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21970600 | ||||||
| chrX:21970707
|
T | TA | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-1189dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970707 | |||||
| chrX:21970718
|
GC | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-1177delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970718 | |||||
| chrX:21970745
|
G | GT | 55 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0097others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.171-1133dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970745 | |||||
| chrX:21970745
|
GT | G | 15 | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0245others(12): Show | 15 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.171-1133delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970745 | |||||
| chrX:21970745
|
GTT | G | 32 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(29): Show | 32 | HG00741.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.171-1134_171-1133d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970745 | |||||
| chrX:21970751
|
T | G | 1 | a0001c0001t0011g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.171-1146T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21970751 | ||||||
| chrX:21970764
|
T | TA | 2 | a0001c0001t0001g0173a0001c0001t0001g0178 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.171-1131dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970764 | |||||
| chrX:21970824
|
C | CA | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-1070dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970824 | |||||
| chrX:21970934
|
C | CT | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-963_171-962ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21970934 | ||||||
| chrX:21970939
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171-958G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21970939 | ||||||
| chrX:21970948
|
A | G | 1 | a0001c0001t0011g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.171-949A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21970948 | ||||||
| chrX:21970967
|
C | CA | 9 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0012others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-929dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21970967 | |||||
| chrX:21971016
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.171-881G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21971016 | ||||||
| chrX:21971025
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.171-872C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21971025 | ||||||
| chrX:21971055
|
G | T | 1 | a0001c0001t0003g0269 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.171-842G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21971055 | ||||||
| chrX:21971066
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.171-831C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21971066 | ||||||
| chrX:21971153
|
G | GT | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0164others(1): Show | 4 | HG01106.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-743dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971153 | |||||
| chrX:21971155
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.171-742C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21971155 | ||||||
| chrX:21971199
|
G | GA | 3 | a0001c0001t0001g0051a0001c0001t0001g0297a0001c0001t0004g0104 | 3 | NA18947.hp1 NA18977.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.171-687dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971199 | |||||
| chrX:21971199
|
GA | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-687delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971199 | |||||
| chrX:21971234
|
G | A | 173 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0070others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.171-663G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21971234 | ||||||
| chrX:21971291
|
T | TAAAA | 89 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.171-604_171-603ins others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971291 | |||||
| chrX:21971343
|
TA | T | 1 | a0001c0001t0001g0039 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.171-549delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971343 | |||||
| chrX:21971372
|
TA | T | 89 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.171-523delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971372 | |||||
| chrX:21971692
|
TA | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-203delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971692 | |||||
| chrX:21971735
|
C | A | 80 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.171-162C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21971735 | ||||||
| chrX:21971792
|
TA | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-102delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971792 | |||||
| chrX:21971839
|
T | TC | 2 | a0001c0001t0001g0056a0001c0001t0001g0084 | 2 | NA18964.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.171-58_171-57insC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | chrX | 21971839 | ||||||
| chrX:21971852
|
GC | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.171-41delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 21971852 | |||||
| chrX:21972095
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0004g0062a0001c0001t0004g0063others(1): Show | 4 | HG00735.hp2 HG01256.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+105A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972095 | ||||||
| chrX:21972104
|
TC | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.264+117delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 21972104 | |||||
| chrX:21972326
|
A | AC | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-181_265-180ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972326 | ||||||
| chrX:21972327
|
AG | A | 1 | a0001c0001t0006g0058 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.265-177delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 21972327 | |||||
| chrX:21972328
|
G | C | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-179G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972328 | ||||||
| chrX:21972329
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-178G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972329 | ||||||
| chrX:21972330
|
G | C | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-177G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972330 | ||||||
| chrX:21972331
|
A | AC | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-176_265-175ins others(1): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972331 | ||||||
| chrX:21972334
|
G | T | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-173G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972334 | ||||||
| chrX:21972335
|
T | C | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-172T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972335 | ||||||
| chrX:21972336
|
T | A | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-171T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972336 | ||||||
| chrX:21972337
|
G | C | 76 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.265-170G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972337 | ||||||
| chrX:21972338
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-169G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972338 | ||||||
| chrX:21972340
|
A | T | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-167A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972340 | ||||||
| chrX:21972347
|
A | T | 1 | a0001c0001t0004g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.265-160A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972347 | ||||||
| chrX:21972424
|
C | T | 1 | a0001c0001t0002g0211 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.265-83C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | chrX | 21972424 | ||||||
| chrX:21972459
|
T | TC | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-46dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 21972459 | |||||
| chrX:21972480
|
GC | G | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.265-24delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 21972480 | |||||
| chrX:21972570
|
CG | C | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | splice_donor_variant&intron_variant | HIGH | c.329+1delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21972570 | |||||
| chrX:21972722
|
A | G | 68 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(65): Show | 68 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.329+151A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21972722 | ||||||
| chrX:21972724
|
T | C | 62 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(59): Show | 62 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.329+153T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21972724 | ||||||
| chrX:21972729
|
C | CA | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+162dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21972729 | |||||
| chrX:21972746
|
T | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.329+175T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21972746 | ||||||
| chrX:21972748
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105 | 3 | HG01515.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.329+177A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21972748 | ||||||
| chrX:21972893
|
TG | T | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.329+325delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21972893 | |||||
| chrX:21972916
|
C | CA | 29 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0021others(26): Show | 29 | HG01106.hp1 HG01891.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.329+369dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21972916 | |||||
| chrX:21972916
|
C | CAA | 31 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0070others(28): Show | 31 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.329+368_329+369dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21972916 | |||||
| chrX:21972916
|
C | CAAA | 6 | a0001c0001t0001g0188a0001c0001t0002g0200a0001c0001t0002g0202others(3): Show | 6 | HG02027.hp1 HG02155.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.329+367_329+369dup others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21972916 | |||||
| chrX:21972916
|
CA | C | 45 | a0001c0001t0001g0081a0001c0001t0001g0108a0001c0001t0001g0117others(42): Show | 45 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.329+369delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21972916 | |||||
| chrX:21972916
|
CAA | C | 2 | a0001c0001t0003g0115a0001c0001t0010g0255 | 2 | HG02809.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.329+368_329+369del others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21972916 | |||||
| chrX:21972981
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.329+410A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21972981 | ||||||
| chrX:21973040
|
G | GC | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+473dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21973040 | |||||
| chrX:21973233
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.329+662C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973233 | ||||||
| chrX:21973266
|
G | A | 1 | a0001c0001t0003g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.329+695G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973266 | ||||||
| chrX:21973288
|
G | A | 7 | a0001c0001t0003g0271a0001c0001t0003g0292a0001c0001t0004g0043others(4): Show | 7 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.329+717G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973288 | ||||||
| chrX:21973307
|
C | T | 7 | a0001c0001t0003g0271a0001c0001t0003g0292a0001c0001t0004g0043others(4): Show | 7 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.329+736C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973307 | ||||||
| chrX:21973311
|
C | G | 1 | a0001c0001t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.329+740C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973311 | ||||||
| chrX:21973351
|
A | C | 88 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.329+780A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973351 | ||||||
| chrX:21973505
|
A | G | 1 | a0001c0001t0003g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.329+934A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973505 | ||||||
| chrX:21973527
|
GT | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+958delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21973527 | |||||
| chrX:21973550
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.329+979C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973550 | ||||||
| chrX:21973554
|
AGGGTG | A | 1 | a0001c0001t0001g0034 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.329+989_329+993del others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21973554 | |||||
| chrX:21973678
|
GA | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+1111delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21973678 | |||||
| chrX:21973738
|
TA | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+1169delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21973738 | |||||
| chrX:21973868
|
TG | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+1299delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21973868 | |||||
| chrX:21973876
|
G | C | 1 | a0001c0001t0002g0197 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.329+1305G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21973876 | ||||||
| chrX:21974038
|
TC | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+1470delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21974038 | |||||
| chrX:21974202
|
C | G | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.329+1631C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21974202 | ||||||
| chrX:21974275
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0002g0130a0001c0001t0002g0131others(2): Show | 5 | HG01070.hp2 HG02109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.329+1704G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21974275 | ||||||
| chrX:21974396
|
C | G | 1 | a0001c0001t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.329+1825C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21974396 | ||||||
| chrX:21974529
|
T | TG | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+1958_329+1959i others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21974529 | ||||||
| chrX:21974675
|
C | CT | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+2110dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21974675 | |||||
| chrX:21974784
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.329+2213G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21974784 | ||||||
| chrX:21974800
|
G | GT | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+2230dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21974800 | |||||
| chrX:21974856
|
CT | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.330-2185delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21974856 | |||||
| chrX:21974856
|
CTT | C | 28 | a0001c0001t0001g0100a0001c0001t0001g0117a0001c0001t0001g0217others(25): Show | 28 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.330-2186_330-2185d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21974856 | |||||
| chrX:21974856
|
CTTT | C | 37 | a0001c0001t0001g0075a0001c0001t0002g0007a0001c0001t0002g0112others(34): Show | 37 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.330-2187_330-2185d others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21974856 | |||||
| chrX:21974866
|
T | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-2195T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21974866 | ||||||
| chrX:21974876
|
T | A | 17 | a0001c0001t0001g0117a0001c0001t0001g0217a0001c0001t0001g0218others(14): Show | 17 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.330-2185T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21974876 | ||||||
| chrX:21975020
|
A | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-2041A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21975020 | ||||||
| chrX:21975085
|
TA | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-1972delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21975085 | |||||
| chrX:21975181
|
G | GA | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-1877dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21975181 | |||||
| chrX:21975193
|
G | GT | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-1867dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21975193 | |||||
| chrX:21975241
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0164a0001c0001t0002g0010 | 3 | HG02970.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.330-1820C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21975241 | ||||||
| chrX:21975328
|
T | TA | 1 | a0001c0001t0002g0214 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.330-1726dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21975328 | |||||
| chrX:21975328
|
TA | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-1726delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21975328 | |||||
| chrX:21975385
|
A | G | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.330-1676A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21975385 | ||||||
| chrX:21975511
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.330-1550C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21975511 | ||||||
| chrX:21975541
|
T | C | 1 | a0001c0001t0006g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.330-1520T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21975541 | ||||||
| chrX:21975562
|
GC | G | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-1497delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21975562 | |||||
| chrX:21975699
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.330-1362A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21975699 | ||||||
| chrX:21975774
|
CG | C | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-1285delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21975774 | |||||
| chrX:21975785
|
A | G | 23 | a0001c0001t0002g0267a0001c0001t0002g0276a0001c0001t0002g0277others(20): Show | 23 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.330-1276A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21975785 | ||||||
| chrX:21975791
|
GT | G | 3 | a0001c0001t0001g0188a0001c0001t0002g0183a0001c0001t0002g0203 | 3 | HG00408.hp2 HG02027.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.330-1268delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21975791 | |||||
| chrX:21976133
|
G | A | 1 | a0001c0001t0003g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.330-928G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21976133 | ||||||
| chrX:21976164
|
C | G | 1 | a0001c0001t0002g0288 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.330-897C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21976164 | ||||||
| chrX:21976179
|
G | C | 1 | a0001c0001t0003g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.330-882G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21976179 | ||||||
| chrX:21976226
|
TG | T | 1 | a0002c0003t0002g0193 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-833delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21976226 | |||||
| chrX:21976565
|
A | C | 134 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0075others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.330-496A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21976565 | ||||||
| chrX:21976588
|
GA | G | 172 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0070others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.330-463delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21976588 | |||||
| chrX:21976680
|
C | CT | 3 | a0001c0001t0006g0014a0001c0001t0006g0082a0001c0001t0006g0119 | 3 | HG02451.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.330-380dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 21976680 | |||||
| chrX:21976850
|
C | T | 41 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(38): Show | 41 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.330-211C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21976850 | ||||||
| chrX:21976950
|
G | T | 1 | a0001c0001t0004g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.330-111G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21976950 | ||||||
| chrX:21976958
|
A | G | 1 | a0001c0001t0001g0002 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.330-103A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21976958 | ||||||
| chrX:21976980
|
T | G | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.330-81T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | chrX | 21976980 | ||||||
| chrX:21977291
|
A | G | 1 | a0001c0001t0005g0275 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.505+55A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 5/10 | chrX | 21977291 | ||||||
| chrX:21977486
|
T | TA | 10 | a0001c0001t0001g0117a0001c0001t0001g0189a0001c0001t0002g0186others(7): Show | 10 | HG02976.hp2 HG03195.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.505+261dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 21977486 | |||||
| chrX:21977486
|
TA | T | 5 | a0001c0001t0001g0145a0001c0001t0002g0130a0001c0001t0002g0131others(2): Show | 5 | HG01070.hp2 HG02109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.505+261delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 21977486 | |||||
| chrX:21977564
|
C | A | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.505+328C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 5/10 | chrX | 21977564 | ||||||
| chrX:21977708
|
C | T | 4 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0005g0266others(1): Show | 4 | HG03041.hp1 HG03516.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-252C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 5/10 | chrX | 21977708 | ||||||
| chrX:21977805
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.506-155C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 5/10 | chrX | 21977805 | ||||||
| chrX:21977810
|
G | GA | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.506-143dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 21977810 | |||||
| chrX:21978345
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0002g0146 | 2 | HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.660+231C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 6/10 | chrX | 21978345 | ||||||
| chrX:21978453
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.660+339T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 6/10 | chrX | 21978453 | ||||||
| chrX:21978583
|
CAAAT | C | 1 | a0001c0001t0004g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.661-291_661-288del others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 21978583 | |||||
| chrX:21978794
|
T | C | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.661-83T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 6/10 | chrX | 21978794 | ||||||
| chrX:21979089
|
T | C | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.750+123T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979089 | ||||||
| chrX:21979167
|
C | G | 52 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(49): Show | 52 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.750+201C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979167 | ||||||
| chrX:21979188
|
C | CT | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.750+233dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979188 | |||||
| chrX:21979188
|
C | CTT | 4 | a0001c0001t0001g0023a0001c0001t0002g0135a0001c0001t0002g0191others(1): Show | 4 | HG03710.hp1 HG03942.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+232_750+233dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979188 | |||||
| chrX:21979188
|
C | CTTT | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.750+231_750+233dup others(3): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979188 | |||||
| chrX:21979241
|
G | A | 1 | a0001c0001t0003g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.750+275G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979241 | ||||||
| chrX:21979277
|
G | T | 1 | a0001c0001t0005g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.750+311G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979277 | ||||||
| chrX:21979378
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.750+412G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979378 | ||||||
| chrX:21979516
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.750+550T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979516 | ||||||
| chrX:21979536
|
T | C | 2 | a0001c0001t0001g0296a0001c0001t0002g0190 | 2 | HG02135.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.750+570T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979536 | ||||||
| chrX:21979574
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0052 | 2 | HG00738.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.750+608G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979574 | ||||||
| chrX:21979611
|
C | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 167 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.750+645C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979611 | ||||||
| chrX:21979846
|
C | A | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.750+880C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979846 | ||||||
| chrX:21979911
|
G | A | 1 | a0001c0001t0011g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.750+945G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979911 | ||||||
| chrX:21979931
|
C | CA | 21 | a0001c0001t0002g0146a0001c0001t0002g0267a0001c0001t0002g0276others(18): Show | 21 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.750+980dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979931 | |||||
| chrX:21979931
|
C | CAA | 1 | a0001c0001t0005g0264 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.750+979_750+980dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979931 | |||||
| chrX:21979931
|
CA | C | 31 | a0001c0001t0001g0041a0001c0001t0001g0117a0001c0001t0001g0188others(28): Show | 31 | HG00735.hp1 HG01081.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.750+980delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979931 | |||||
| chrX:21979953
|
T | TA | 7 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 8 | NA18944.hp1 NA18964.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.750+998dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979953 | |||||
| chrX:21979953
|
TA | T | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0136 | 3 | HG02109.hp2 HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.750+998delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979953 | |||||
| chrX:21979964
|
A | G | 5 | a0001c0001t0003g0133a0001c0001t0003g0259a0001c0001t0003g0265others(2): Show | 5 | HG01109.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.750+998A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21979964 | ||||||
| chrX:21979967
|
TTAATAA | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG01106.hp1 HG02698.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.750+1011_750+1016d others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21979967 | |||||
| chrX:21980132
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.750+1166A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980132 | ||||||
| chrX:21980134
|
T | G | 1 | a0001c0001t0001g0039 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.750+1168T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980134 | ||||||
| chrX:21980174
|
ATAATT | A | 1 | a0001c0001t0001g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.750+1212_750+1216d others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980174 | |||||
| chrX:21980283
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.750+1317G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980283 | ||||||
| chrX:21980332
|
G | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0082a0001c0001t0006g0119 | 3 | HG02451.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.750+1366G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980332 | ||||||
| chrX:21980415
|
C | CA | 36 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(33): Show | 36 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.750+1464dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980415 | |||||
| chrX:21980415
|
C | CAA | 15 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0110others(12): Show | 15 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.750+1463_750+1464d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980415 | |||||
| chrX:21980415
|
C | CAAAA | 1 | a0001c0001t0003g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.750+1461_750+1464d others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980415 | |||||
| chrX:21980415
|
C | CAAAAA | 2 | a0001c0001t0003g0012a0001c0001t0005g0013 | 2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.750+1460_750+1464d others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980415 | |||||
| chrX:21980415
|
C | CAAAAAA | 3 | a0001c0001t0001g0076a0001c0001t0001g0164a0001c0001t0002g0010 | 3 | HG02970.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.750+1459_750+1464d others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980415 | |||||
| chrX:21980415
|
C | CAAAAAAA | 1 | a0001c0001t0001g0242 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.750+1458_750+1464d others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980415 | |||||
| chrX:21980425
|
A | AAT | 1 | a0001c0001t0004g0068 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.750+1460_750+1461i others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980425 | |||||
| chrX:21980427
|
A | AAT | 1 | a0001c0001t0004g0104 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.750+1462_750+1463i others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980427 | |||||
| chrX:21980427
|
A | AATAT | 1 | a0001c0001t0004g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.750+1462_750+1463i others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980427 | |||||
| chrX:21980427
|
A | T | 1 | a0001c0001t0004g0068 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.750+1461A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980427 | ||||||
| chrX:21980429
|
A | AAAAAAAA others(1): Show |
3 | a0001c0001t0001g0075a0001c0001t0001g0106a0001c0001t0001g0108 | 3 | HG01106.hp1 NA19004.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.750+1464_750+1465i others(10): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAAAAT | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(91): Show | 95 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.750+1464_750+1465i others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAAAAT others(2): Show |
6 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0038others(3): Show | 6 | HG03710.hp1 HG03831.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+1464_750+1465i others(11): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAAAAT others(4): Show |
2 | a0001c0001t0002g0160a0001c0001t0002g0161 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.750+1464_750+1465i others(13): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAAAT | 4 | a0001c0001t0001g0044a0001c0001t0001g0162a0001c0001t0001g0227others(1): Show | 4 | HG02683.hp2 HG03704.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+1464_750+1465i others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAAATA others(1): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0055others(3): Show | 6 | HG00738.hp1 HG02273.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+1464_750+1465i others(10): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAAATA others(3): Show |
2 | a0001c0001t0001g0015a0001c0001t0002g0192 | 2 | HG02683.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.750+1464_750+1465i others(12): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAAATA others(5): Show |
2 | a0001c0001t0002g0195a0001c0001t0002g0220 | 2 | HG02071.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.750+1464_750+1465i others(14): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAAATA others(7): Show |
1 | a0001c0001t0002g0205 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.750+1464_750+1465i others(16): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAATAT | 7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0042others(4): Show | 7 | HG01358.hp1 HG02015.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.750+1464_750+1465i others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAATAT others(2): Show |
2 | a0001c0001t0001g0036a0001c0001t0002g0185 | 2 | HG01099.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.750+1464_750+1465i others(11): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAATAT others(4): Show |
25 | a0001c0001t0001g0040a0001c0001t0001g0070a0001c0001t0001g0087others(22): Show | 25 | HG00558.hp2 HG00639.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.750+1464_750+1465i others(13): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAAATAT others(6): Show |
7 | a0001c0001t0001g0045a0001c0001t0002g0183a0001c0001t0002g0186others(4): Show | 7 | HG00099.hp1 HG00408.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.750+1464_750+1465i others(15): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAATATA others(3): Show |
2 | a0001c0001t0002g0196a0001c0001t0002g0199 | 2 | NA19001.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.750+1464_750+1465i others(12): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0003g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.750+1464_750+1465i others(14): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0002g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.750+1464_750+1465i others(18): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAATATAT others(4): Show |
1 | a0001c0001t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.750+1464_750+1465i others(13): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AAT | 6 | a0001c0001t0001g0145a0001c0001t0001g0254a0001c0001t0002g0131others(3): Show | 6 | HG01070.hp2 HG01074.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.750+1486_750+1487d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | AATATAT | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.750+1482_750+1487d others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21980429 | |||||
| chrX:21980429
|
A | ATAT | 2 | a0001c0001t0002g0130a0001c0001t0002g0136 | 2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.750+1463_750+1464i others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980429 | ||||||
| chrX:21980429
|
A | T | 18 | a0001c0001t0003g0011a0001c0001t0003g0159a0001c0001t0003g0175others(15): Show | 18 | HG00735.hp1 HG01081.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.750+1463A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980429 | ||||||
| chrX:21980431
|
T | A | 62 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(59): Show | 62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.750+1465T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980431 | ||||||
| chrX:21980433
|
T | A | 54 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(51): Show | 54 | HG00741.hp1 HG01109.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.750+1467T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980433 | ||||||
| chrX:21980454
|
T | A | 1 | a0001c0001t0004g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.750+1488T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980454 | ||||||
| chrX:21980513
|
A | T | 1 | a0001c0001t0001g0018 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.750+1547A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980513 | ||||||
| chrX:21980559
|
C | T | 13 | a0001c0001t0003g0113a0001c0001t0003g0124a0001c0001t0003g0147others(10): Show | 13 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.750+1593C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21980559 | ||||||
| chrX:21981063
|
G | T | 17 | a0001c0001t0003g0011a0001c0001t0003g0159a0001c0001t0003g0215others(14): Show | 17 | HG00735.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.750+2097G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981063 | ||||||
| chrX:21981090
|
G | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0082a0001c0001t0006g0119 | 3 | HG02451.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.750+2124G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981090 | ||||||
| chrX:21981271
|
G | A | 37 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(34): Show | 37 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.750+2305G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981271 | ||||||
| chrX:21981319
|
C | CA | 88 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0070others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.750+2364dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21981319 | |||||
| chrX:21981376
|
AG | A | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.750+2416delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21981376 | |||||
| chrX:21981377
|
G | C | 4 | a0001c0001t0002g0155a0001c0001t0002g0287a0001c0001t0002g0289others(1): Show | 4 | HG02723.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2411G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981377 | ||||||
| chrX:21981472
|
T | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 214 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.750+2506T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981472 | ||||||
| chrX:21981473
|
A | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 214 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.750+2507A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981473 | ||||||
| chrX:21981576
|
G | A | 3 | a0001c0001t0005g0272a0001c0001t0005g0273a0001c0001t0006g0083 | 3 | HG00099.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.750+2610G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981576 | ||||||
| chrX:21981793
|
G | A | 40 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(37): Show | 40 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.751-2511G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981793 | ||||||
| chrX:21981841
|
C | G | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.751-2463C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21981841 | ||||||
| chrX:21981871
|
C | CAAGTCAG others(5): Show |
11 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064others(8): Show | 11 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.751-2430_751-2429i others(14): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21981871 | |||||
| chrX:21982024
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.751-2280A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21982024 | ||||||
| chrX:21982051
|
AG | A | 1 | a0001c0001t0005g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.751-2251delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21982051 | |||||
| chrX:21982336
|
C | CA | 17 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0076others(14): Show | 17 | HG00621.hp1 HG01192.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.751-1948dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21982336 | |||||
| chrX:21982336
|
C | CAA | 1 | a0001c0001t0005g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.751-1949_751-1948d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21982336 | |||||
| chrX:21982336
|
CA | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0227a0001c0001t0005g0275 | 3 | HG02976.hp2 NA18951.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.751-1948delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21982336 | |||||
| chrX:21982533
|
C | T | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG01256.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.751-1771C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21982533 | ||||||
| chrX:21982622
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.751-1682G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21982622 | ||||||
| chrX:21982724
|
A | C | 2 | a0001c0001t0003g0165a0001c0001t0003g0167 | 2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.751-1580A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21982724 | ||||||
| chrX:21982870
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 8 | NA18944.hp1 NA18964.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.751-1434A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21982870 | ||||||
| chrX:21982940
|
G | GA | 1 | a0001c0001t0005g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.751-1360dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21982940 | |||||
| chrX:21983005
|
G | C | 1 | a0001c0001t0006g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.751-1299G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983005 | ||||||
| chrX:21983035
|
CT | C | 1 | a0001c0001t0005g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.751-1262delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21983035 | |||||
| chrX:21983042
|
T | A | 1 | a0001c0001t0004g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.751-1262T>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983042 | ||||||
| chrX:21983043
|
A | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 211 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.751-1261A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983043 | ||||||
| chrX:21983090
|
A | G | 2 | a0001c0001t0003g0165a0001c0001t0003g0167 | 2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.751-1214A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983090 | ||||||
| chrX:21983104
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.751-1200A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983104 | ||||||
| chrX:21983127
|
A | G | 1 | a0001c0001t0011g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.751-1177A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983127 | ||||||
| chrX:21983135
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.751-1169G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983135 | ||||||
| chrX:21983171
|
C | T | 2 | a0001c0001t0004g0066a0001c0001t0004g0103 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.751-1133C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983171 | ||||||
| chrX:21983281
|
C | A | 1 | a0001c0001t0001g0242 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.751-1023C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983281 | ||||||
| chrX:21983322
|
TG | T | 1 | a0001c0001t0005g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.751-979delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21983322 | |||||
| chrX:21983402
|
A | AT | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 208 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.751-892dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21983402 | |||||
| chrX:21983402
|
A | ATT | 1 | a0001c0001t0012g0048 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.751-893_751-892dup others(2): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21983402 | |||||
| chrX:21983402
|
AT | A | 2 | a0001c0001t0003g0285a0001c0005t0001g0219 | 2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.751-892delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 21983402 | |||||
| chrX:21983413
|
G | T | 1 | a0001c0001t0003g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.751-891G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983413 | ||||||
| chrX:21983681
|
G | A | 62 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(59): Show | 62 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.751-623G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983681 | ||||||
| chrX:21983705
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.751-599T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983705 | ||||||
| chrX:21983750
|
C | T | 61 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.751-554C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983750 | ||||||
| chrX:21983779
|
A | T | 1 | a0001c0001t0001g0078 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.751-525A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983779 | ||||||
| chrX:21983811
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 126 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.751-493C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983811 | ||||||
| chrX:21983894
|
A | C | 1 | a0001c0001t0001g0015 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.751-410A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983894 | ||||||
| chrX:21983952
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.751-352A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21983952 | ||||||
| chrX:21984124
|
A | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0061 | 2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.751-180A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | chrX | 21984124 | ||||||
| chrX:21984444
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.865+26A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | chrX | 21984444 | ||||||
| chrX:21984513
|
GT | G | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.865+100delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 21984513 | |||||
| chrX:21984585
|
GC | G | 1 | a0001c0001t0005g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.865+169delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 21984585 | |||||
| chrX:21984593
|
A | G | 63 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(60): Show | 63 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.865+175A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | chrX | 21984593 | ||||||
| chrX:21984738
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.865+320G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | chrX | 21984738 | ||||||
| chrX:21984866
|
GC | G | 1 | a0001c0001t0005g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.866-273delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 21984866 | |||||
| chrX:21985022
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.866-122T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | chrX | 21985022 | ||||||
| chrX:21985044
|
CT | C | 1 | a0001c0001t0005g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.866-95delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 21985044 | |||||
| chrX:21985112
|
T | C | 41 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0070others(38): Show | 41 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.866-32T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | chrX | 21985112 | ||||||
| chrX:21985348
|
C | G | 1 | a0001c0001t0004g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.945+125C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21985348 | ||||||
| chrX:21985629
|
A | G | 1 | a0001c0001t0011g0139 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.945+406A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21985629 | ||||||
| chrX:21985647
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.945+424C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21985647 | ||||||
| chrX:21985975
|
C | T | 4 | a0001c0001t0002g0192a0001c0001t0002g0196a0001c0001t0002g0200others(1): Show | 4 | HG02155.hp2 HG02165.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+752C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21985975 | ||||||
| chrX:21986065
|
G | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(181): Show | 185 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.945+842G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21986065 | ||||||
| chrX:21986230
|
TC | T | 1 | a0001c0001t0005g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.945+1010delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986230 | |||||
| chrX:21986256
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.945+1033G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21986256 | ||||||
| chrX:21986290
|
G | A | 37 | a0001c0001t0001g0075a0001c0001t0002g0007a0001c0001t0002g0112others(34): Show | 37 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.945+1067G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21986290 | ||||||
| chrX:21986347
|
C | CA | 11 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0236others(8): Show | 11 | HG00140.hp1 HG00642.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.945+1152dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986347
|
C | CAA | 5 | a0001c0001t0003g0133a0001c0001t0003g0259a0001c0001t0003g0268others(2): Show | 5 | HG01243.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.945+1151_945+1152d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986347
|
C | CAAA | 1 | a0001c0001t0003g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.945+1150_945+1152d others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986347
|
CA | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0038others(14): Show | 17 | HG00544.hp2 HG00735.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.945+1152delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986347
|
CAA | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(135): Show | 139 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.945+1151_945+1152d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986347
|
CAAA | C | 17 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0055others(14): Show | 17 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.945+1150_945+1152d others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986347
|
CAAAA | C | 3 | a0001c0001t0005g0264a0001c0001t0006g0058a0001c0001t0011g0139 | 3 | HG02723.hp1 HG04184.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.945+1149_945+1152d others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986347
|
CAAAAA | C | 54 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(51): Show | 54 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.945+1148_945+1152d others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986347
|
CAAAAAA | C | 5 | a0001c0001t0004g0066a0001c0001t0004g0074a0001c0001t0005g0275others(2): Show | 5 | HG01167.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+1147_945+1152d others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986347 | |||||
| chrX:21986398
|
C | A | 61 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.945+1175C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21986398 | ||||||
| chrX:21986601
|
A | G | 107 | a0001c0001t0001g0075a0001c0001t0002g0007a0001c0001t0002g0112others(104): Show | 107 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.945+1378A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21986601 | ||||||
| chrX:21986625
|
C | G | 61 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.945+1402C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21986625 | ||||||
| chrX:21986710
|
A | G | 40 | a0001c0001t0001g0075a0001c0001t0002g0007a0001c0001t0002g0112others(37): Show | 40 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.945+1487A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21986710 | ||||||
| chrX:21986995
|
G | GT | 122 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(119): Show | 123 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.945+1789dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986995 | |||||
| chrX:21986995
|
G | GTT | 70 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0096others(67): Show | 70 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.945+1788_945+1789d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986995 | |||||
| chrX:21986995
|
G | GTTT | 43 | a0001c0001t0001g0075a0001c0001t0002g0007a0001c0001t0002g0112others(40): Show | 43 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.945+1787_945+1789d others(5): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986995 | |||||
| chrX:21986995
|
G | GTTTT | 9 | a0001c0001t0002g0137a0001c0001t0003g0133a0001c0001t0003g0150others(6): Show | 9 | HG00673.hp1 HG01109.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.945+1786_945+1789d others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986995 | |||||
| chrX:21986995
|
GT | G | 1 | a0001c0001t0001g0250 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.945+1789delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21986995 | |||||
| chrX:21987026
|
G | A | 1 | a0001c0001t0003g0260 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.945+1803G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21987026 | ||||||
| chrX:21987112
|
C | T | 1 | a0001c0001t0004g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.945+1889C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21987112 | ||||||
| chrX:21987248
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 8 | NA18944.hp1 NA18964.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.945+2025C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21987248 | ||||||
| chrX:21987253
|
TC | T | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.945+2033delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21987253 | |||||
| chrX:21987297
|
A | G | 1 | a0001c0001t0006g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.945+2074A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21987297 | ||||||
| chrX:21987343
|
A | AT | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.945+2127dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21987343 | |||||
| chrX:21987523
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.945+2300A>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21987523 | ||||||
| chrX:21988282
|
G | GT | 12 | a0001c0001t0002g0180a0001c0001t0004g0062a0001c0001t0004g0063others(9): Show | 12 | HG00597.hp2 HG00735.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.945+3068dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988282 | |||||
| chrX:21988308
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.945+3085G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988308 | ||||||
| chrX:21988320
|
AC | A | 1 | a0001c0001t0002g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.945+3100delC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988320 | |||||
| chrX:21988321
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.945+3098C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988321 | ||||||
| chrX:21988377
|
T | G | 6 | a0001c0001t0001g0145a0001c0001t0002g0130a0001c0001t0002g0131others(3): Show | 6 | HG01070.hp2 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.945+3154T>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988377 | ||||||
| chrX:21988387
|
C | T | 61 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.945+3164C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988387 | ||||||
| chrX:21988388
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0080a0002c0003t0002g0193 | 3 | HG02155.hp1 NA18948.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.945+3165G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988388 | ||||||
| chrX:21988393
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0081 | 2 | HG03239.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.945+3170C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988393 | ||||||
| chrX:21988420
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.945+3197C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988420 | ||||||
| chrX:21988527
|
C | T | 3 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0064 | 3 | HG01256.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.945+3304C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988527 | ||||||
| chrX:21988653
|
ACT | A | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.945+3433_945+3434d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988653 | |||||
| chrX:21988662
|
C | CA | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.945+3469dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAA | 1 | a0001c0001t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.945+3468_945+3469d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(2): Show |
1 | a0001c0001t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.945+3461_945+3469d others(11): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0217a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG00140.hp1 HG02165.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.945+3458_945+3469d others(14): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(6): Show |
9 | a0001c0001t0001g0117a0001c0001t0001g0218a0001c0001t0001g0231others(6): Show | 9 | HG00323.hp1 HG01074.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.945+3457_945+3469d others(15): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0035a0001c0001t0001g0250a0001c0001t0002g0131others(2): Show | 5 | HG00423.hp1 HG02109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.945+3456_945+3469d others(16): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0003 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.945+3455_945+3469d others(17): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0223a0001c0001t0001g0235others(1): Show | 4 | HG02523.hp2 NA19065.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+3453_945+3469d others(19): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(11): Show |
9 | a0001c0001t0001g0187a0001c0001t0001g0224a0001c0001t0001g0234others(6): Show | 9 | HG00544.hp2 HG01928.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.945+3452_945+3469d others(20): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0242a0001c0001t0007g0239 | 2 | HG00642.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.945+3451_945+3469d others(21): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0241 | 2 | HG00639.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.945+3450_945+3469d others(22): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0256 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.945+3449_945+3469d others(23): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0227a0001c0001t0001g0294 | 2 | NA18951.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.945+3448_945+3469d others(24): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0295 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.945+3447_945+3469d others(25): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0076a0001c0001t0001g0236 | 2 | HG02970.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.945+3445_945+3469d others(27): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CA | C | 1 | a0001c0001t0002g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.945+3469delA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CAA | C | 1 | a0001c0001t0001g0145 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.945+3468_945+3469d others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CAAAAAAA others(2): Show |
C | 5 | a0001c0001t0001g0244a0001c0001t0002g0137a0001c0001t0003g0150others(2): Show | 5 | HG00438.hp2 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.945+3461_945+3469d others(11): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CAAAAAAA others(3): Show |
C | 41 | a0001c0001t0001g0075a0001c0001t0002g0007a0001c0001t0002g0112others(38): Show | 41 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.945+3460_945+3469d others(12): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0050others(4): Show | 7 | HG02056.hp1 NA18943.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.945+3459_945+3469d others(13): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CAAAAAAA others(5): Show |
C | 128 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(125): Show | 129 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.945+3458_945+3469d others(14): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0029a0001c0001t0009g0047 | 2 | NA18959.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.945+3457_945+3469d others(15): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0003g0121a0001c0001t0005g0263a0001c0001t0005g0275others(4): Show | 7 | HG02723.hp1 HG03579.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.945+3454_945+3469d others(18): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988662
|
CAAAAAAA others(10): Show |
C | 54 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(51): Show | 54 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.945+3453_945+3469d others(19): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21988662 | |||||
| chrX:21988689
|
AAAAG | A | 1 | a0001c0001t0002g0180 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.945+3467_945+3470d others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988689 | ||||||
| chrX:21988878
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0238 | 2 | NA18942.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.945+3655A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988878 | ||||||
| chrX:21988884
|
T | C | 1 | a0001c0001t0003g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.945+3661T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21988884 | ||||||
| chrX:21989469
|
C | T | 61 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.946-3128C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21989469 | ||||||
| chrX:21989535
|
A | T | 1 | a0001c0001t0001g0041 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.946-3062A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21989535 | ||||||
| chrX:21989634
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(92): Show | 96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.946-2963A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21989634 | ||||||
| chrX:21989695
|
G | A | 1 | a0001c0001t0005g0280 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.946-2902G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21989695 | ||||||
| chrX:21989806
|
G | C | 3 | a0001c0001t0004g0142a0001c0001t0004g0163a0001c0005t0001g0219 | 3 | HG02809.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.946-2791G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21989806 | ||||||
| chrX:21989850
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.946-2747C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21989850 | ||||||
| chrX:21989868
|
G | A | 2 | a0001c0002t0003g0149a0001c0002t0003g0169 | 2 | HG01081.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.946-2729G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21989868 | ||||||
| chrX:21990028
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.946-2569C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21990028 | ||||||
| chrX:21990132
|
T | TA | 1 | a0001c0001t0002g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.946-2464dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21990132 | |||||
| chrX:21990152
|
A | AG | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.946-2443dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21990152 | |||||
| chrX:21990259
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.946-2338C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21990259 | ||||||
| chrX:21990290
|
A | T | 4 | a0001c0001t0001g0023a0001c0001t0002g0135a0001c0001t0002g0191others(1): Show | 4 | HG03710.hp1 HG03942.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.946-2307A>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21990290 | ||||||
| chrX:21990320
|
C | T | 36 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(33): Show | 36 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.946-2277C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21990320 | ||||||
| chrX:21990487
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0178 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.946-2110C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21990487 | ||||||
| chrX:21990717
|
G | A | 36 | a0001c0001t0002g0007a0001c0001t0002g0112a0001c0001t0002g0114others(33): Show | 36 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.946-1880G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21990717 | ||||||
| chrX:21990721
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.946-1876A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21990721 | ||||||
| chrX:21990866
|
C | T | 98 | a0001c0001t0001g0075a0001c0001t0002g0007a0001c0001t0002g0112others(95): Show | 98 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.946-1731C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21990866 | ||||||
| chrX:21991317
|
A | G | 1 | a0001c0001t0003g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.946-1280A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21991317 | ||||||
| chrX:21991883
|
A | AG | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.946-712dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 21991883 | |||||
| chrX:21991948
|
T | C | 63 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(60): Show | 63 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.946-649T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21991948 | ||||||
| chrX:21992136
|
G | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0018others(92): Show | 96 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.946-461G>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21992136 | ||||||
| chrX:21992407
|
G | C | 1 | a0001c0001t0003g0154 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.946-190G>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | chrX | 21992407 | ||||||
| chrX:21992808
|
C | G | 6 | a0001c0001t0003g0128a0001c0001t0003g0150a0001c0001t0003g0154others(3): Show | 6 | HG02080.hp1 HG02738.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+96C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21992808 | ||||||
| chrX:21992857
|
T | TG | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+147dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21992857 | |||||
| chrX:21992897
|
A | AG | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+186dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21992897 | |||||
| chrX:21992924
|
T | TC | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+213dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21992924 | |||||
| chrX:21992939
|
CT | C | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+230delT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21992939 | |||||
| chrX:21992954
|
T | TA | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+244dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21992954 | |||||
| chrX:21992975
|
C | CT | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+264dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21992975 | |||||
| chrX:21993012
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1061+300A>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993012 | ||||||
| chrX:21993086
|
C | CCT | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+374_1061+375i others(4): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993086 | ||||||
| chrX:21993115
|
A | AC | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+405dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21993115 | |||||
| chrX:21993289
|
G | GA | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1061+578dupA | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21993289 | |||||
| chrX:21993318
|
G | A | 59 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0011others(56): Show | 59 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1061+606G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993318 | ||||||
| chrX:21993410
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1061+698T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993410 | ||||||
| chrX:21993499
|
G | A | 1 | a0001c0001t0004g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1061+787G>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993499 | ||||||
| chrX:21993505
|
G | GT | 2 | a0001c0001t0002g0116a0001c0001t0004g0141 | 2 | HG00140.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1061+800dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21993505 | |||||
| chrX:21993520
|
A | AG | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1062-789dupG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21993520 | |||||
| chrX:21993566
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1062-746C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993566 | ||||||
| chrX:21993655
|
AG | A | 1 | a0001c0001t0001g0080 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1062-653delG | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21993655 | |||||
| chrX:21993683
|
G | GT | 1 | a0001c0001t0001g0080 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1062-628dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21993683 | |||||
| chrX:21993758
|
A | AT | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1062-549dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21993758 | |||||
| chrX:21993812
|
C | T | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1062-500C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993812 | ||||||
| chrX:21993936
|
C | T | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1062-376C>T | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993936 | ||||||
| chrX:21993937
|
T | C | 1 | a0001c0001t0009g0047 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1062-375T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21993937 | ||||||
| chrX:21993993
|
T | TC | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1062-314dupC | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21993993 | |||||
| chrX:21994083
|
C | A | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1062-229C>A | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21994083 | ||||||
| chrX:21994098
|
T | C | 3 | a0001c0001t0004g0174a0001c0002t0003g0149a0001c0002t0003g0169 | 3 | HG01081.hp2 HG02293.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1062-214T>C | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21994098 | ||||||
| chrX:21994178
|
C | G | 1 | a0001c0001t0003g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1062-134C>G | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | chrX | 21994178 | ||||||
| chrX:21994269
|
C | CT | 1 | a0004c0004t0013g0293 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1062-41dupT | SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 21994269 |