Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4478 |
|---|---|
| ensemblid | ENSG00000147065.18 |
| hgncid | 7373 |
| symbol | MSN |
| name | moesin |
| refseq_nuc | NM_002444.3 |
| refseq_prot | NP_002435.1 |
| ensembl_nuc | ENST00000360270.7 |
| ensembl_prot | ENSP00000353408.5 |
| mane_status | MANE Select |
| chr | chrX |
| start | 65667654 |
| end | 65741931 |
| strand | + |
| ver | v1.2 |
| region | chrX:65667654-65741931 |
| region5000 | chrX:65662654-65746931 |
| regionname0 | MSN_chrX_65667654_65741931 |
| regionname5000 | MSN_chrX_65662654_65746931 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2227 | 112 | 3 | 19 | 67 | 7 | 14 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0002 | 0/0 | 2227 | 36 | 33 | 2 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0003 | 0/0 | 2227 | 5 | 5 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0004 | 0/0 | 2227 | 4 | 3 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0005 | 0/0 | 2227 | 3 | 3 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0006 | 0/0 | 2227 | 2 | 0 | 2 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0007 | 0/0 | 2227 | 2 | 2 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0008 | 0/0 | 2227 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0009 | 0/0 | 2227 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0010 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0011 | 0/0 | 2227 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0012 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| t0013 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1734 | 169 | 52 | 26 | 66 | 7 | 16 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0002c0002 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3960 | 111 | 3 | 19 | 66 | 7 | 14 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0002 | 0/0 | 3960 | 36 | 33 | 2 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0003 | 0/0 | 3960 | 5 | 5 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0004 | 0/0 | 3960 | 4 | 3 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0005 | 0/0 | 3960 | 3 | 3 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0006 | 0/0 | 3960 | 2 | 0 | 2 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0007 | 0/0 | 3960 | 2 | 2 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0008 | 0/0 | 3960 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0009 | 0/0 | 3960 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0010 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0011 | 0/0 | 3960 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0012 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0001c0001t0013 | 0/0 | 3960 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| a0002c0002t0001 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | copy fasta | chrX | 65662654 | 65746931 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0001c0001t0013g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01074 | hp1 | a0001 | c0001 | t0009 | g0101 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01081 | hp2 | a0001 | c0001 | t0011 | g0043 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0040 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0094 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | LWK | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0123 | AFR | LWK | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ASW | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ASW | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | GIH | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | MSL | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | USA | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0146 | REF | REF | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0060 | REF | REF | MSN_chrX_65662654_65746931 | MSN | chrX | 65662654 | 65746931 |
| 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:65735399
|
C | CG | 1 | a0002 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.931dupG | p.Glu311fs | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/13 | 1120/3960 | 932/1734 | 311/577 | INFO_REALIGN_3_PRIME | chrX | 65735399 | |
| chrX:65736803
|
TG | T | 1 | a0002 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.970delG | p.Glu324fs | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 9/13 | 1158/3960 | 970/1734 | 324/577 | INFO_REALIGN_3_PRIME | chrX | 65736803 | |
| chrX:65736856
|
GA | G | 1 | a0002 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1023delA | p.Glu341fs | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 9/13 | 1211/3960 | 1023/1734 | 341/577 | INFO_REALIGN_3_PRIME | chrX | 65736856 | |
| chrX:65736885
|
G | GC | 1 | a0002 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1051dupC | p.Leu351fs | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 9/13 | 1240/3960 | 1052/1734 | 351/577 | INFO_REALIGN_3_PRIME | chrX | 65736885 |
| 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 |
|---|
| 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:65667676
|
G | A | 1 | a0001c0001t0008 | 1 | HG04199.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-166G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/13 | chrX | 65667676 | ||||||
| chrX:65740396
|
C | T | 3 | a0001c0001t0003a0001c0001t0004a0001c0001t0013 | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*503C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 503 | chrX | 65740396 | |||||
| chrX:65740569
|
C | G | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(7): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*676C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 676 | chrX | 65740569 | |||||
| chrX:65740647
|
G | A | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(7): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*754G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 754 | chrX | 65740647 | |||||
| chrX:65740785
|
A | G | 1 | a0001c0001t0013 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 892 | chrX | 65740785 | |||||
| chrX:65740939
|
A | G | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | 54 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1046A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1046 | chrX | 65740939 | |||||
| chrX:65740969
|
G | A | 1 | a0001c0001t0009 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1076G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1076 | chrX | 65740969 | |||||
| chrX:65741027
|
A | G | 1 | a0001c0001t0005 | 3 | HG02630.hp2 HG02896.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1134A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1134 | chrX | 65741027 | |||||
| chrX:65741386
|
A | C | 10 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(7): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1493A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1493 | chrX | 65741386 | |||||
| chrX:65741557
|
C | T | 2 | a0001c0001t0004a0001c0001t0013 | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1664C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1664 | chrX | 65741557 | |||||
| chrX:65741574
|
C | G | 1 | a0001c0001t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1681C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1681 | chrX | 65741574 | |||||
| chrX:65741648
|
C | G | 1 | a0001c0001t0007 | 2 | HG02258.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1755C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1755 | chrX | 65741648 | |||||
| chrX:65741700
|
C | T | 1 | a0001c0001t0011 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1807C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1807 | chrX | 65741700 | |||||
| chrX:65741740
|
G | A | 1 | a0001c0001t0007 | 2 | HG02258.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1847G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1847 | chrX | 65741740 | |||||
| chrX:65741795
|
G | A | 1 | a0001c0001t0010 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1902G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 13/13 | 1902 | chrX | 65741795 |
| 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:65667935
|
C | A | 1 | a0001c0001t0003g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.12+82C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65667935 | ||||||
| chrX:65667945
|
GC | G | 1 | a0001c0001t0001g0161 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.12+95delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65667945 | |||||
| chrX:65667998
|
G | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG00140.hp1 HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.12+145G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65667998 | ||||||
| chrX:65668026
|
AG | A | 1 | a0001c0001t0001g0161 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.12+177delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65668026 | |||||
| chrX:65668190
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.12+337T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65668190 | ||||||
| chrX:65668210
|
TC | T | 1 | a0001c0001t0001g0161 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.12+361delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65668210 | |||||
| chrX:65668262
|
A | AG | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+413dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65668262 | |||||
| chrX:65668468
|
AC | A | 1 | a0001c0001t0001g0161 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.12+619delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65668468 | |||||
| chrX:65668494
|
G | GT | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+644dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65668494 | |||||
| chrX:65668595
|
T | C | 41 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(38): Show | 46 | HG00738.hp1 HG01081.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.12+742T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65668595 | ||||||
| chrX:65668695
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+842G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65668695 | ||||||
| chrX:65668737
|
T | TG | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+885dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65668737 | |||||
| chrX:65668972
|
TG | T | 1 | a0001c0001t0001g0161 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.12+1122delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65668972 | |||||
| chrX:65669173
|
C | A | 1 | a0001c0001t0002g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.12+1320C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65669173 | ||||||
| chrX:65669228
|
TG | T | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+1377delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65669228 | |||||
| chrX:65669370
|
TG | T | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+1520delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65669370 | |||||
| chrX:65669667
|
A | AGAGGGCT others(5): Show |
1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+1815_12+1826dup others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65669667 | |||||
| chrX:65669823
|
CT | C | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+1972delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65669823 | |||||
| chrX:65669825
|
T | TA | 2 | a0001c0001t0001g0046a0001c0001t0004g0047 | 2 | HG00735.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.12+1983dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65669825 | |||||
| chrX:65669825
|
TA | T | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.12+1983delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65669825 | |||||
| chrX:65669832
|
A | C | 1 | a0001c0001t0002g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.12+1979A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65669832 | ||||||
| chrX:65669855
|
T | A | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+2002T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65669855 | ||||||
| chrX:65670237
|
G | GA | 2 | a0001c0001t0006g0016a0001c0001t0006g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.12+2390dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670237 | |||||
| chrX:65670314
|
G | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+2461G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670314 | ||||||
| chrX:65670426
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0011g0043 | 2 | HG01081.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.12+2573A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670426 | ||||||
| chrX:65670429
|
TG | T | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+2577delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670429 | ||||||
| chrX:65670443
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+2590A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670443 | ||||||
| chrX:65670451
|
G | T | 1 | a0001c0001t0002g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.12+2598G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670451 | ||||||
| chrX:65670728
|
C | CA | 1 | a0001c0001t0001g0052 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.12+2882dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670728 | |||||
| chrX:65670737
|
C | CA | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+2891dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670737 | |||||
| chrX:65670859
|
AT | A | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+3008delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670859 | |||||
| chrX:65670895
|
G | GTT | 1 | a0001c0001t0011g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.12+3043_12+3044dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670895 | |||||
| chrX:65670896
|
T | TTA | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG02071.hp1 HG02976.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3101_12+3102dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
T | TTATA | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12+3099_12+3102dup others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
T | TTATATA | 2 | a0001c0001t0001g0054a0001c0001t0002g0018 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.12+3097_12+3102dup others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.12+3091_12+3102dup others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTA | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 7 | HG01943.hp1 HG01952.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+3101_12+3102del others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATA | T | 29 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0069others(26): Show | 29 | HG00642.hp1 HG01099.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.12+3099_12+3102del others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATA | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0093others(20): Show | 25 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.12+3097_12+3102del others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(1): Show |
T | 21 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0108others(18): Show | 22 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.12+3095_12+3102del others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(3): Show |
T | 20 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(17): Show | 20 | HG00140.hp1 HG01358.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.12+3093_12+3102del others(10): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(5): Show |
T | 15 | a0001c0001t0001g0007a0001c0001t0001g0138a0001c0001t0001g0139others(12): Show | 15 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.12+3091_12+3102del others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(7): Show |
T | 10 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0002g0001others(7): Show | 14 | HG02280.hp1 HG02630.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+3089_12+3102del others(14): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(9): Show |
T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA19060.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.12+3087_12+3102del others(16): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(11): Show |
T | 1 | a0001c0001t0001g0148 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.12+3085_12+3102del others(18): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(13): Show |
T | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0002g0037 | 3 | HG01169.hp2 HG02109.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.12+3083_12+3102del others(20): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(15): Show |
T | 4 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0007g0038others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+3081_12+3102del others(22): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(17): Show |
T | 2 | a0001c0001t0001g0153a0001c0001t0010g0040 | 2 | HG02630.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.12+3079_12+3102del others(24): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(19): Show |
T | 1 | a0001c0001t0002g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.12+3077_12+3102del others(26): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(21): Show |
T | 1 | a0001c0001t0002g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.12+3075_12+3102del others(28): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(25): Show |
T | 2 | a0001c0001t0001g0154a0002c0002t0001g0155 | 2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.12+3071_12+3102del others(32): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670896
|
TTATATAT others(33): Show |
T | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG00738.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.12+3063_12+3102del others(40): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670896 | |||||
| chrX:65670898
|
A | T | 1 | a0001c0001t0002g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.12+3045A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670898 | ||||||
| chrX:65670944
|
ATATATAT others(4): Show |
A | 3 | a0001c0001t0001g0124a0001c0001t0002g0044a0001c0001t0013g0123 | 3 | HG02647.hp1 NA18966.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.12+3093_12+3103del others(11): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670944 | |||||
| chrX:65670946
|
ATATATAT others(2): Show |
A | 2 | a0001c0001t0001g0106a0001c0001t0002g0023 | 2 | HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.12+3095_12+3103del others(9): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670946 | |||||
| chrX:65670948
|
ATATATAT | A | 1 | a0001c0001t0001g0092 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.12+3097_12+3103del others(7): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65670948 | |||||
| chrX:65670954
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.12+3101A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65670954 | ||||||
| chrX:65671009
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.12+3156A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671009 | ||||||
| chrX:65671092
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.12+3239C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671092 | ||||||
| chrX:65671308
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.12+3455C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671308 | ||||||
| chrX:65671319
|
AG | A | 1 | a0001c0001t0001g0068 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.12+3467delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671319 | ||||||
| chrX:65671691
|
G | A | 1 | a0001c0001t0013g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.12+3838G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671691 | ||||||
| chrX:65671967
|
C | G | 2 | a0001c0001t0006g0016a0001c0001t0006g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.12+4114C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65671967 | ||||||
| chrX:65672221
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0137 | 2 | HG02135.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.12+4368C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672221 | ||||||
| chrX:65672545
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.12+4692A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672545 | ||||||
| chrX:65672876
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.12+5023C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672876 | ||||||
| chrX:65672944
|
T | G | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+5091T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672944 | ||||||
| chrX:65672968
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.12+5115C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65672968 | ||||||
| chrX:65673459
|
C | CT | 9 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(6): Show | 10 | HG00738.hp1 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+5621dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65673459 | |||||
| chrX:65673459
|
CT | C | 4 | a0001c0001t0001g0069a0001c0001t0002g0032a0001c0001t0002g0041others(1): Show | 4 | HG01099.hp1 HG02630.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+5621delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65673459 | |||||
| chrX:65673547
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0010g0040 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.12+5694C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65673547 | ||||||
| chrX:65673604
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+5751G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65673604 | ||||||
| chrX:65673864
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.12+6011A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65673864 | ||||||
| chrX:65674094
|
A | C | 1 | a0001c0001t0004g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.12+6241A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674094 | ||||||
| chrX:65674266
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.12+6413C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674266 | ||||||
| chrX:65674274
|
T | G | 1 | a0001c0001t0002g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.12+6421T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674274 | ||||||
| chrX:65674576
|
T | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+6723T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674576 | ||||||
| chrX:65674591
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+6738T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674591 | ||||||
| chrX:65674685
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.12+6832T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65674685 | ||||||
| chrX:65675335
|
T | A | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+7482T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65675335 | ||||||
| chrX:65675498
|
A | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+7645A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65675498 | ||||||
| chrX:65675642
|
AT | A | 1 | a0001c0001t0001g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.12+7802delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65675642 | |||||
| chrX:65675786
|
C | T | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+7933C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65675786 | ||||||
| chrX:65675929
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+8076C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65675929 | ||||||
| chrX:65676208
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+8355G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676208 | ||||||
| chrX:65676300
|
G | A | 1 | a0001c0001t0007g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.12+8447G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676300 | ||||||
| chrX:65676301
|
A | C | 3 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037 | 3 | HG02109.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.12+8448A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676301 | ||||||
| chrX:65676637
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12+8784G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676637 | ||||||
| chrX:65676974
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+9121G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676974 | ||||||
| chrX:65676985
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+9132C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65676985 | ||||||
| chrX:65676999
|
A | AT | 2 | a0001c0001t0002g0031a0001c0001t0002g0034 | 2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.12+9154dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65676999 | |||||
| chrX:65677033
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.12+9180G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677033 | ||||||
| chrX:65677062
|
G | A | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(46): Show | 54 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.12+9209G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677062 | ||||||
| chrX:65677108
|
G | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | NA18971.hp1 NA18986.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+9255G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677108 | ||||||
| chrX:65677349
|
T | C | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+9496T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677349 | ||||||
| chrX:65677506
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+9653C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677506 | ||||||
| chrX:65677563
|
G | C | 1 | a0001c0001t0011g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.12+9710G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677563 | ||||||
| chrX:65677626
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0002g0010 | 2 | HG01099.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.12+9773C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65677626 | ||||||
| chrX:65678213
|
C | CCTT | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+10361_12+10363d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65678213 | |||||
| chrX:65678217
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+10364T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678217 | ||||||
| chrX:65678220
|
T | G | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+10367T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678220 | ||||||
| chrX:65678222
|
C | G | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+10369C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678222 | ||||||
| chrX:65678295
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.12+10442G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678295 | ||||||
| chrX:65678347
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.12+10494T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65678347 | ||||||
| chrX:65679102
|
T | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(48): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.12+11249T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65679102 | ||||||
| chrX:65679280
|
G | C | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+11427G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65679280 | ||||||
| chrX:65679444
|
T | TA | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.12+11592dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65679444 | |||||
| chrX:65679767
|
T | A | 30 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(27): Show | 35 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.12+11914T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65679767 | ||||||
| chrX:65679869
|
G | A | 1 | a0001c0001t0003g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.12+12016G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65679869 | ||||||
| chrX:65680492
|
AT | A | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.12+12641delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65680492 | |||||
| chrX:65680588
|
T | C | 30 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(27): Show | 35 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.12+12735T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65680588 | ||||||
| chrX:65680747
|
T | C | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.12+12894T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65680747 | ||||||
| chrX:65680939
|
A | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(157): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.12+13086A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65680939 | ||||||
| chrX:65681054
|
A | AT | 2 | a0001c0001t0006g0016a0001c0001t0006g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.12+13211dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65681054 | |||||
| chrX:65681729
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+13876A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65681729 | ||||||
| chrX:65681734
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12+13881C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65681734 | ||||||
| chrX:65681920
|
AT | A | 1 | a0001c0001t0001g0073 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.12+14077delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65681920 | |||||
| chrX:65681943
|
T | G | 1 | a0001c0001t0008g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.12+14090T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65681943 | ||||||
| chrX:65681957
|
A | G | 8 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(5): Show | 9 | HG00738.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+14104A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65681957 | ||||||
| chrX:65682170
|
G | T | 1 | a0001c0001t0002g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.12+14317G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65682170 | ||||||
| chrX:65682237
|
T | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(48): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.12+14384T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65682237 | ||||||
| chrX:65682823
|
A | G | 1 | a0001c0001t0013g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.12+14970A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65682823 | ||||||
| chrX:65682898
|
C | T | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+15045C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65682898 | ||||||
| chrX:65683012
|
C | CAG | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+15160_12+15161d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683012 | |||||
| chrX:65683023
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+15170G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683023 | ||||||
| chrX:65683383
|
T | TGCC | 16 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0009others(13): Show | 17 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.12+15540_12+15542d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683383 | |||||
| chrX:65683383
|
T | TGCCGCCG others(2): Show |
1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+15534_12+15542d others(11): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683383 | |||||
| chrX:65683393
|
G | GCCA | 13 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0057others(10): Show | 14 | HG00609.hp1 HG01069.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.12+15588_12+15590d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | |||||
| chrX:65683393
|
G | GCCACCAC others(5): Show |
5 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0001g0108others(2): Show | 5 | NA18960.hp1 NA18974.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+15579_12+15590d others(14): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | |||||
| chrX:65683393
|
G | GCCACCAC others(8): Show |
3 | a0001c0001t0001g0063a0001c0001t0001g0068a0001c0001t0001g0074 | 3 | HG02027.hp1 NA18965.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.12+15576_12+15590d others(17): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | |||||
| chrX:65683393
|
G | GCCGCCA | 3 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0026 | 3 | HG00738.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.12+15542_12+15543i others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | |||||
| chrX:65683393
|
GCCA | G | 15 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0023others(12): Show | 19 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.12+15588_12+15590d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | |||||
| chrX:65683393
|
GCCACCAC others(8): Show |
G | 7 | a0001c0001t0001g0003a0001c0001t0001g0090a0001c0001t0001g0092others(4): Show | 8 | HG00621.hp1 HG02083.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+15576_12+15590d others(17): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683393 | |||||
| chrX:65683396
|
A | G | 18 | a0001c0001t0001g0054a0001c0001t0002g0014a0001c0001t0002g0019others(15): Show | 18 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.12+15543A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683396 | ||||||
| chrX:65683399
|
A | G | 17 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0014others(14): Show | 21 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.12+15546A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683399 | ||||||
| chrX:65683442
|
C | CCACCACC others(10): Show |
1 | a0001c0001t0001g0147 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.12+15590_12+15591i others(19): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683442 | |||||
| chrX:65683443
|
C | CA | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.12+15590_12+15591i others(3): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683443 | ||||||
| chrX:65683552
|
T | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0096 | 2 | HG02040.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.12+15699T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683552 | ||||||
| chrX:65683703
|
A | G | 10 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(7): Show | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.12+15850A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683703 | ||||||
| chrX:65683941
|
TC | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 5 | HG00642.hp1 HG00735.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+16089delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65683941 | ||||||
| chrX:65683942
|
C | CT | 9 | a0001c0001t0001g0057a0001c0001t0001g0087a0001c0001t0002g0014others(6): Show | 9 | HG00735.hp2 HG02300.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.12+16105dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683942 | |||||
| chrX:65683942
|
CT | C | 11 | a0001c0001t0001g0158a0001c0001t0002g0008a0001c0001t0002g0009others(8): Show | 11 | HG00738.hp1 HG01081.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.12+16105delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65683942 | |||||
| chrX:65684057
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0024 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.12+16204C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684057 | ||||||
| chrX:65684065
|
C | T | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+16212C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684065 | ||||||
| chrX:65684194
|
G | T | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+16341G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684194 | ||||||
| chrX:65684322
|
T | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+16469T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684322 | ||||||
| chrX:65684433
|
TC | T | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12+16581delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684433 | ||||||
| chrX:65684443
|
C | CT | 1 | a0001c0001t0001g0068 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.12+16602dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65684443 | |||||
| chrX:65684502
|
G | A | 1 | a0001c0001t0005g0033 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.12+16649G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684502 | ||||||
| chrX:65684507
|
C | T | 4 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0010g0040others(1): Show | 4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+16654C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684507 | ||||||
| chrX:65684532
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+16679G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684532 | ||||||
| chrX:65684777
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.12+16924T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684777 | ||||||
| chrX:65684824
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.12+16971C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684824 | ||||||
| chrX:65684855
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+17002C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684855 | ||||||
| chrX:65684981
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.12+17128C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65684981 | ||||||
| chrX:65685111
|
T | A | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+17258T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685111 | ||||||
| chrX:65685530
|
G | A | 4 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0010g0040others(1): Show | 4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+17677G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685530 | ||||||
| chrX:65685588
|
GTT | G | 1 | a0001c0001t0004g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.12+17739_12+17740d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65685588 | |||||
| chrX:65685661
|
T | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.12+17808T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685661 | ||||||
| chrX:65685671
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.12+17818C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685671 | ||||||
| chrX:65685723
|
G | A | 1 | a0001c0001t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.12+17870G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685723 | ||||||
| chrX:65685904
|
A | AC | 1 | a0001c0001t0001g0150 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.12+18057dupC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65685904 | |||||
| chrX:65685906
|
C | A | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+18053C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65685906 | ||||||
| chrX:65686189
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12+18336T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65686189 | ||||||
| chrX:65686940
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.12+19087C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65686940 | ||||||
| chrX:65687174
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+19321G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65687174 | ||||||
| chrX:65687243
|
G | A | 32 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(29): Show | 37 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.12+19390G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65687243 | ||||||
| chrX:65687548
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0026others(2): Show | 6 | HG02717.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+19695G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65687548 | ||||||
| chrX:65687936
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+20083C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65687936 | ||||||
| chrX:65688268
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.12+20415G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65688268 | ||||||
| chrX:65688297
|
C | T | 1 | a0001c0001t0010g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.12+20444C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65688297 | ||||||
| chrX:65688645
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.12+20792G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65688645 | ||||||
| chrX:65689213
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.12+21360T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65689213 | ||||||
| chrX:65689220
|
C | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+21367C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65689220 | ||||||
| chrX:65689927
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+22074A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65689927 | ||||||
| chrX:65690086
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+22233T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65690086 | ||||||
| chrX:65690390
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.12+22537A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65690390 | ||||||
| chrX:65690856
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0137 | 2 | HG02135.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.12+23003G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65690856 | ||||||
| chrX:65690919
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.12+23066T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65690919 | ||||||
| chrX:65691333
|
T | C | 1 | a0001c0001t0010g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.12+23480T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691333 | ||||||
| chrX:65691405
|
G | A | 4 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0010g0040others(1): Show | 4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+23552G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691405 | ||||||
| chrX:65691565
|
T | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(48): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.12+23712T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691565 | ||||||
| chrX:65691673
|
T | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0062 | 2 | NA19066.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.12+23820T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691673 | ||||||
| chrX:65691995
|
G | A | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0097 | 3 | NA18955.hp1 NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.12+24142G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65691995 | ||||||
| chrX:65692008
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.12+24155G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692008 | ||||||
| chrX:65692030
|
C | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+24177C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692030 | ||||||
| chrX:65692202
|
G | C | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12+24349G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692202 | ||||||
| chrX:65692442
|
G | A | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(23): Show | 31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.13-24376G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692442 | ||||||
| chrX:65692613
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.13-24205T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692613 | ||||||
| chrX:65692653
|
AT | A | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-24159delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65692653 | |||||
| chrX:65692664
|
G | GT | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-24151dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65692664 | |||||
| chrX:65692682
|
GT | G | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-24132delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65692682 | |||||
| chrX:65692781
|
G | GT | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-24037_13-24036i others(3): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692781 | ||||||
| chrX:65692789
|
C | CCT | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-24028_13-24027d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65692789 | |||||
| chrX:65692793
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13-24025C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692793 | ||||||
| chrX:65692794
|
C | CTCACCTC others(4): Show |
1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-24021_13-24020i others(13): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65692794 | |||||
| chrX:65692823
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23995G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692823 | ||||||
| chrX:65692824
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23994C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692824 | ||||||
| chrX:65692825
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23993G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692825 | ||||||
| chrX:65692846
|
AT | A | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23967delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65692846 | |||||
| chrX:65692932
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.13-23886G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65692932 | ||||||
| chrX:65692942
|
GT | G | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23869delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65692942 | |||||
| chrX:65693026
|
C | CTT | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23790_13-23789d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693026 | |||||
| chrX:65693084
|
T | TC | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23733dupC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693084 | |||||
| chrX:65693177
|
CA | C | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23638delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693177 | |||||
| chrX:65693277
|
AT | A | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23535delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693277 | |||||
| chrX:65693286
|
AG | A | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23529delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693286 | |||||
| chrX:65693363
|
GT | G | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23452delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693363 | |||||
| chrX:65693428
|
C | CT | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23387dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693428 | |||||
| chrX:65693438
|
TG | T | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23377delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693438 | |||||
| chrX:65693585
|
TG | T | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23227delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693585 | |||||
| chrX:65693639
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.13-23179G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693639 | ||||||
| chrX:65693648
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-23170A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693648 | ||||||
| chrX:65693736
|
AC | A | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23080delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693736 | |||||
| chrX:65693792
|
G | A | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-23026G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693792 | ||||||
| chrX:65693803
|
C | A | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23015C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693803 | ||||||
| chrX:65693804
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23014A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693804 | ||||||
| chrX:65693805
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-23013G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693805 | ||||||
| chrX:65693876
|
A | AC | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-22938dupC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693876 | |||||
| chrX:65693880
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13-22938C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65693880 | ||||||
| chrX:65693934
|
TC | T | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.13-22881delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65693934 | |||||
| chrX:65694075
|
C | CA | 2 | a0001c0001t0002g0011a0001c0001t0002g0019 | 2 | HG02896.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.13-22731dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65694075 | |||||
| chrX:65694083
|
A | C | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-22735A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694083 | ||||||
| chrX:65694332
|
A | AT | 4 | a0001c0001t0001g0095a0001c0001t0001g0104a0001c0001t0001g0120others(1): Show | 4 | HG00621.hp1 HG02056.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-22471dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65694332 | |||||
| chrX:65694332
|
AT | A | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.13-22471delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65694332 | |||||
| chrX:65694368
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.13-22450C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694368 | ||||||
| chrX:65694453
|
C | T | 1 | a0001c0001t0004g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.13-22365C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694453 | ||||||
| chrX:65694538
|
G | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0023others(7): Show | 14 | HG01243.hp1 HG02145.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.13-22280G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694538 | ||||||
| chrX:65694588
|
A | C | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-22230A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694588 | ||||||
| chrX:65694636
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-22182C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694636 | ||||||
| chrX:65694772
|
G | GT | 1 | a0001c0001t0001g0046 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.13-22045dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65694772 | |||||
| chrX:65694781
|
A | G | 1 | a0001c0001t0011g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.13-22037A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694781 | ||||||
| chrX:65694911
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.13-21907G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694911 | ||||||
| chrX:65694914
|
G | C | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-21904G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65694914 | ||||||
| chrX:65695081
|
C | CGT | 4 | a0001c0001t0001g0089a0001c0001t0001g0105a0001c0001t0006g0016others(1): Show | 4 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-21709_13-21708d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | |||||
| chrX:65695081
|
C | CGTGT | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13-21711_13-21708d others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | |||||
| chrX:65695081
|
CGT | C | 5 | a0001c0001t0002g0009a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG02615.hp1 HG02976.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-21709_13-21708d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | |||||
| chrX:65695081
|
CGTGT | C | 4 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0011others(1): Show | 4 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-21711_13-21708d others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | |||||
| chrX:65695081
|
CGTGTGT | C | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-21713_13-21708d others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695081 | |||||
| chrX:65695104
|
GTGT | G | 32 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(29): Show | 37 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.13-21713_13-21711d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695104 | ||||||
| chrX:65695191
|
A | G | 10 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(7): Show | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-21627A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695191 | ||||||
| chrX:65695248
|
C | G | 1 | a0001c0001t0002g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.13-21570C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695248 | ||||||
| chrX:65695266
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0012g0015 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13-21552T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695266 | ||||||
| chrX:65695507
|
C | CA | 15 | a0001c0001t0001g0052a0001c0001t0001g0062a0001c0001t0001g0068others(12): Show | 15 | HG00735.hp2 HG01081.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.13-21284dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695507 | |||||
| chrX:65695507
|
C | CAA | 8 | a0001c0001t0002g0008a0001c0001t0003g0048a0001c0001t0003g0049others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.13-21285_13-21284d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695507 | |||||
| chrX:65695507
|
C | CAAA | 3 | a0001c0001t0002g0021a0001c0001t0003g0006a0001c0001t0003g0050 | 3 | HG02055.hp1 HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.13-21286_13-21284d others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695507 | |||||
| chrX:65695507
|
CA | C | 35 | a0001c0001t0001g0057a0001c0001t0001g0076a0001c0001t0001g0103others(32): Show | 40 | HG00738.hp1 HG01081.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.13-21284delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695507 | |||||
| chrX:65695522
|
A | AAAC | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-21294_13-21293i others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695522 | |||||
| chrX:65695525
|
A | C | 1 | a0001c0001t0002g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.13-21293A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695525 | ||||||
| chrX:65695532
|
A | AAAAAAC | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13-21284_13-21283i others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695532 | |||||
| chrX:65695611
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0012 | 3 | HG00738.hp1 HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.13-21207G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695611 | ||||||
| chrX:65695886
|
A | AGAGTTTT others(26): Show |
38 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(35): Show | 43 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.13-20930_13-20929i others(35): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65695886 | |||||
| chrX:65695933
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.13-20885G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65695933 | ||||||
| chrX:65696196
|
CA | C | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-20615delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696196 | |||||
| chrX:65696225
|
T | TCACA | 3 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0011g0043 | 3 | HG01081.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.13-20569_13-20566d others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | |||||
| chrX:65696225
|
T | TCACACA | 4 | a0001c0001t0002g0024a0001c0001t0004g0047a0001c0001t0004g0056others(1): Show | 4 | HG00735.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-20571_13-20566d others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | |||||
| chrX:65696225
|
T | TCACACAC others(1): Show |
4 | a0001c0001t0002g0014a0001c0001t0002g0045a0001c0001t0004g0126others(1): Show | 4 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-20573_13-20566d others(10): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | |||||
| chrX:65696225
|
T | TCACACAC others(3): Show |
11 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0018others(8): Show | 12 | HG00738.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-20575_13-20566d others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | |||||
| chrX:65696225
|
T | TCACACAC others(5): Show |
23 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0010others(20): Show | 27 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.13-20577_13-20566d others(14): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | |||||
| chrX:65696225
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0003g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.13-20579_13-20566d others(16): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | |||||
| chrX:65696225
|
T | TCACACAC others(9): Show |
1 | a0001c0001t0002g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.13-20581_13-20566d others(18): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | |||||
| chrX:65696225
|
T | TCACACAC others(11): Show |
2 | a0001c0001t0002g0009a0001c0001t0002g0025 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.13-20583_13-20566d others(20): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65696225 | |||||
| chrX:65696480
|
G | C | 1 | a0001c0001t0001g0004 | 2 | HG00609.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.13-20338G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65696480 | ||||||
| chrX:65696546
|
C | A | 1 | a0001c0001t0013g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13-20272C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65696546 | ||||||
| chrX:65697013
|
G | C | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(24): Show | 32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.13-19805G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65697013 | ||||||
| chrX:65698232
|
G | A | 9 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0108others(6): Show | 9 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.13-18586G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65698232 | ||||||
| chrX:65699052
|
A | T | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(23): Show | 31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.13-17766A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699052 | ||||||
| chrX:65699059
|
G | T | 1 | a0001c0001t0002g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.13-17759G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699059 | ||||||
| chrX:65699315
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0004g0125 | 2 | NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.13-17503G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699315 | ||||||
| chrX:65699641
|
C | T | 6 | a0001c0001t0001g0052a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | NA18970.hp1 NA18989.hp1 NA19067.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-17177C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699641 | ||||||
| chrX:65699748
|
C | CA | 5 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0087others(2): Show | 5 | HG02135.hp1 HG02300.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-17048dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65699748 | |||||
| chrX:65699748
|
CA | C | 32 | a0001c0001t0001g0067a0001c0001t0001g0137a0001c0001t0001g0151others(29): Show | 37 | HG01081.hp2 HG01167.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.13-17048delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65699748 | |||||
| chrX:65699748
|
CAA | C | 10 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(7): Show | 10 | HG00738.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.13-17049_13-17048d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65699748 | |||||
| chrX:65699748
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-17060_13-17048d others(15): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65699748 | |||||
| chrX:65699759
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13-17059A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699759 | ||||||
| chrX:65699791
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-17027C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699791 | ||||||
| chrX:65699921
|
T | C | 6 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(3): Show | 6 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-16897T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65699921 | ||||||
| chrX:65700350
|
G | A | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-16468G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700350 | ||||||
| chrX:65700379
|
T | C | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-16439T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700379 | ||||||
| chrX:65700800
|
C | T | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-16018C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700800 | ||||||
| chrX:65700841
|
A | G | 39 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(36): Show | 44 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.13-15977A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700841 | ||||||
| chrX:65700968
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13-15850A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65700968 | ||||||
| chrX:65701407
|
TG | T | 1 | a0001c0001t0001g0063 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.13-15407delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65701407 | |||||
| chrX:65701770
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-15048A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65701770 | ||||||
| chrX:65701995
|
G | A | 4 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0010g0040others(1): Show | 4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-14823G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65701995 | ||||||
| chrX:65702007
|
C | CT | 16 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0102others(13): Show | 16 | HG00673.hp1 HG00735.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.13-14795dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702007 | |||||
| chrX:65702007
|
CT | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0150a0001c0001t0002g0020others(1): Show | 4 | HG02451.hp1 HG03471.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-14795delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702007 | |||||
| chrX:65702022
|
T | C | 2 | a0001c0001t0006g0016a0001c0001t0006g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.13-14796T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702022 | ||||||
| chrX:65702164
|
C | T | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-14654C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702164 | ||||||
| chrX:65702259
|
C | T | 1 | a0001c0001t0007g0039 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.13-14559C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702259 | ||||||
| chrX:65702260
|
G | A | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-14558G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702260 | ||||||
| chrX:65702499
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-14319C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702499 | ||||||
| chrX:65702659
|
CTG | C | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(23): Show | 31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.13-14157_13-14156d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702659 | |||||
| chrX:65702664
|
T | TAAAAC | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13-14129_13-14125d others(7): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702664 | |||||
| chrX:65702710
|
T | TGG | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.13-14107_13-14106d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702710 | |||||
| chrX:65702728
|
GT | G | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.13-14087delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702728 | |||||
| chrX:65702846
|
GA | G | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.13-13968delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702846 | |||||
| chrX:65702948
|
TA | T | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.13-13866delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65702948 | |||||
| chrX:65702967
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-13851A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65702967 | ||||||
| chrX:65703023
|
T | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-13795T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703023 | ||||||
| chrX:65703035
|
TTTCCCTG | T | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-13782_13-13776d others(9): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703035 | ||||||
| chrX:65703053
|
T | TC | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-13763dupC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65703053 | |||||
| chrX:65703223
|
C | CT | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-13592dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65703223 | |||||
| chrX:65703327
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13-13491A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703327 | ||||||
| chrX:65703370
|
A | AG | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-13446dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65703370 | |||||
| chrX:65703571
|
G | GT | 5 | a0001c0001t0001g0146a0001c0001t0001g0156a0001c0001t0002g0044others(2): Show | 5 | HG01081.hp2 HG02647.hp1 NA19075.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-13238dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65703571 | |||||
| chrX:65703741
|
A | AT | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-13072dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65703741 | |||||
| chrX:65703803
|
C | T | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-13015C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703803 | ||||||
| chrX:65703814
|
T | C | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-13004T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703814 | ||||||
| chrX:65703815
|
G | T | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-13003G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703815 | ||||||
| chrX:65703817
|
T | TC | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-13001_13-13000i others(3): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703817 | ||||||
| chrX:65703904
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-12914G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65703904 | ||||||
| chrX:65704230
|
G | GC | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-12587dupC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704230 | |||||
| chrX:65704374
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.13-12444T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65704374 | ||||||
| chrX:65704421
|
GC | G | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-12395delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704421 | |||||
| chrX:65704433
|
G | A | 2 | a0001c0001t0001g0154a0002c0002t0001g0155 | 2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.13-12385G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65704433 | ||||||
| chrX:65704448
|
G | GT | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-12368dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704448 | |||||
| chrX:65704667
|
G | GT | 27 | a0001c0001t0001g0156a0001c0001t0002g0001a0001c0001t0002g0002others(24): Show | 32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.13-12141dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704667 | |||||
| chrX:65704771
|
G | GT | 6 | a0001c0001t0001g0007a0001c0001t0002g0045a0001c0001t0004g0056others(3): Show | 6 | HG01256.hp1 HG02615.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.13-12031dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704771 | |||||
| chrX:65704771
|
G | GTT | 1 | a0001c0001t0004g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.13-12032_13-12031d others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704771 | |||||
| chrX:65704771
|
GT | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0156a0001c0001t0002g0009 | 3 | NA19030.hp2 NA19075.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.13-12031delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65704771 | |||||
| chrX:65704855
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13-11963C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65704855 | ||||||
| chrX:65704923
|
C | A | 1 | a0001c0001t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-11895C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65704923 | ||||||
| chrX:65705063
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0121 | 2 | NA18995.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.13-11755G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705063 | ||||||
| chrX:65705063
|
G | GC | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-11752dupC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65705063 | |||||
| chrX:65705160
|
TC | T | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-11654delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65705160 | |||||
| chrX:65705203
|
C | G | 39 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(36): Show | 44 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.13-11615C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705203 | ||||||
| chrX:65705357
|
TG | T | 1 | a0001c0001t0002g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.13-11459delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65705357 | |||||
| chrX:65705563
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-11255A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705563 | ||||||
| chrX:65705641
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.13-11177T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705641 | ||||||
| chrX:65705665
|
C | T | 1 | a0001c0001t0009g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.13-11153C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705665 | ||||||
| chrX:65705897
|
GT | G | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.13-10919delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65705897 | |||||
| chrX:65705905
|
T | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.13-10913T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65705905 | ||||||
| chrX:65705928
|
TG | T | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-10887delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65705928 | |||||
| chrX:65706466
|
C | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(46): Show | 54 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.13-10352C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65706466 | ||||||
| chrX:65706836
|
G | A | 3 | a0001c0001t0002g0023a0001c0001t0002g0025a0001c0001t0002g0028 | 3 | HG02145.hp1 HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.13-9982G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65706836 | ||||||
| chrX:65707093
|
A | AG | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-9722dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65707093 | |||||
| chrX:65707195
|
GC | G | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-9620delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65707195 | |||||
| chrX:65707333
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.13-9485G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65707333 | ||||||
| chrX:65707410
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-9408A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65707410 | ||||||
| chrX:65707545
|
G | C | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-9273G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65707545 | ||||||
| chrX:65707776
|
TG | T | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-9039delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65707776 | |||||
| chrX:65707813
|
TTAATC | T | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.13-9001_13-8997del others(5): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65707813 | |||||
| chrX:65707931
|
A | ACT | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-8886_13-8885ins others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65707931 | |||||
| chrX:65707989
|
A | AT | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-8825dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65707989 | |||||
| chrX:65708037
|
A | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0118 | 2 | HG00673.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.13-8781A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708037 | ||||||
| chrX:65708052
|
A | AT | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-8764dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65708052 | |||||
| chrX:65708075
|
T | C | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-8743T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708075 | ||||||
| chrX:65708138
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13-8680G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708138 | ||||||
| chrX:65708583
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.13-8235G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708583 | ||||||
| chrX:65708705
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.13-8113C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708705 | ||||||
| chrX:65708775
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.13-8043C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708775 | ||||||
| chrX:65708808
|
G | C | 4 | a0001c0001t0002g0001a0001c0001t0002g0030a0001c0001t0005g0001others(1): Show | 8 | HG01243.hp1 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.13-8010G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65708808 | ||||||
| chrX:65709040
|
C | T | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-7778C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65709040 | ||||||
| chrX:65709096
|
G | C | 1 | a0001c0001t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-7722G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65709096 | ||||||
| chrX:65709495
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-7323C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65709495 | ||||||
| chrX:65709843
|
C | G | 1 | a0001c0001t0003g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.13-6975C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65709843 | ||||||
| chrX:65710310
|
C | T | 2 | a0001c0001t0006g0016a0001c0001t0006g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.13-6508C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710310 | ||||||
| chrX:65710420
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.13-6398T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710420 | ||||||
| chrX:65710537
|
G | T | 1 | a0001c0001t0002g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13-6281G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710537 | ||||||
| chrX:65710553
|
T | TG | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-6265_13-6264ins others(1): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710553 | ||||||
| chrX:65710562
|
C | CAAATAA | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-6235_13-6230dup others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65710562 | |||||
| chrX:65710562
|
CAAATAA | C | 1 | a0001c0001t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-6235_13-6230del others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65710562 | |||||
| chrX:65710883
|
GTAT | G | 33 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(30): Show | 38 | HG01081.hp2 HG01243.hp1 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.13-5924_13-5922del others(3): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65710883 | |||||
| chrX:65710980
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.13-5838G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65710980 | ||||||
| chrX:65711084
|
G | GT | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.13-5730dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65711084 | |||||
| chrX:65711249
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.13-5569T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65711249 | ||||||
| chrX:65711697
|
G | T | 1 | a0001c0001t0004g0047 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.13-5121G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65711697 | ||||||
| chrX:65711701
|
C | G | 1 | a0001c0001t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13-5117C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65711701 | ||||||
| chrX:65711996
|
A | G | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-4822A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65711996 | ||||||
| chrX:65712172
|
A | T | 1 | a0001c0001t0002g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.13-4646A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65712172 | ||||||
| chrX:65712416
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0118 | 2 | HG00673.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.13-4402A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65712416 | ||||||
| chrX:65712546
|
A | AT | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-4254dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65712546 | |||||
| chrX:65712546
|
AT | A | 3 | a0001c0001t0002g0020a0001c0001t0003g0049a0001c0001t0004g0125 | 3 | HG02280.hp2 HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.13-4254delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65712546 | |||||
| chrX:65712546
|
ATT | A | 4 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0126others(1): Show | 4 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.13-4255_13-4254del others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65712546 | |||||
| chrX:65712602
|
C | G | 1 | a0001c0001t0002g0027 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.13-4216C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65712602 | ||||||
| chrX:65712914
|
G | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-3904G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65712914 | ||||||
| chrX:65713028
|
G | A | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-3790G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713028 | ||||||
| chrX:65713157
|
C | A | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-3661C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713157 | ||||||
| chrX:65713918
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0114 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.13-2900T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713918 | ||||||
| chrX:65713977
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.13-2841G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713977 | ||||||
| chrX:65713989
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.13-2829A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65713989 | ||||||
| chrX:65714208
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.13-2610A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714208 | ||||||
| chrX:65714279
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.13-2539C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714279 | ||||||
| chrX:65714391
|
A | T | 10 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(7): Show | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-2427A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714391 | ||||||
| chrX:65714458
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0117 | 3 | NA18943.hp1 NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.13-2360T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714458 | ||||||
| chrX:65714720
|
T | A | 1 | a0001c0001t0002g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.13-2098T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714720 | ||||||
| chrX:65714859
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13-1959C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714859 | ||||||
| chrX:65714908
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.13-1910C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714908 | ||||||
| chrX:65714926
|
G | T | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-1892G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714926 | ||||||
| chrX:65714949
|
A | G | 1 | a0001c0001t0002g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.13-1869A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65714949 | ||||||
| chrX:65714979
|
A | ATAGAGTT others(967): Show |
1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13-1825_13-1824ins others(974): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65714979 | |||||
| chrX:65715281
|
T | TAGGATTG others(6): Show |
1 | a0001c0001t0002g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.13-1536_13-1524dup others(13): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 65715281 | |||||
| chrX:65715717
|
G | A | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-1101G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65715717 | ||||||
| chrX:65716178
|
C | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0139 | 2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.13-640C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716178 | ||||||
| chrX:65716287
|
T | G | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.13-531T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716287 | ||||||
| chrX:65716437
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.13-381G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716437 | ||||||
| chrX:65716572
|
G | A | 1 | a0001c0001t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.13-246G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716572 | ||||||
| chrX:65716604
|
T | C | 2 | a0001c0001t0002g0023a0001c0001t0002g0028 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.13-214T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 1/12 | chrX | 65716604 | ||||||
| chrX:65717108
|
A | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+207A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717108 | ||||||
| chrX:65717108
|
A | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.96+207A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717108 | ||||||
| chrX:65717289
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0140 | 2 | HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.96+388G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717289 | ||||||
| chrX:65717431
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+530C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717431 | ||||||
| chrX:65717435
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+534A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717435 | ||||||
| chrX:65717746
|
G | A | 1 | a0001c0001t0002g0012 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.96+845G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717746 | ||||||
| chrX:65717909
|
G | A | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(23): Show | 31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+1008G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65717909 | ||||||
| chrX:65718148
|
A | G | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96+1247A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718148 | ||||||
| chrX:65718175
|
T | C | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(24): Show | 32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.96+1274T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718175 | ||||||
| chrX:65718277
|
G | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(48): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.96+1376G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718277 | ||||||
| chrX:65718470
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.96+1569A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718470 | ||||||
| chrX:65718583
|
T | G | 1 | a0001c0001t0002g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+1682T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718583 | ||||||
| chrX:65718728
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.96+1827G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65718728 | ||||||
| chrX:65718818
|
T | TAAAAAAA | 2 | a0001c0001t0002g0036a0001c0001t0005g0033 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.96+1928_96+1934dup others(7): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718818 | |||||
| chrX:65718818
|
T | TAAAAAAA others(1): Show |
22 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(19): Show | 27 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.96+1927_96+1934dup others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718818 | |||||
| chrX:65718818
|
T | TAAAAAAA others(2): Show |
2 | a0001c0001t0002g0021a0001c0001t0002g0032 | 2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.96+1926_96+1934dup others(9): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718818 | |||||
| chrX:65718818
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+1925_96+1934dup others(10): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718818 | |||||
| chrX:65718818
|
TA | T | 7 | a0001c0001t0001g0085a0001c0001t0001g0103a0001c0001t0001g0135others(4): Show | 7 | HG02015.hp1 HG02074.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+1934delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718818 | |||||
| chrX:65718841
|
G | GA | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.96+1945dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718841 | |||||
| chrX:65718931
|
G | GGA | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.96+2032_96+2033dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65718931 | |||||
| chrX:65719414
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.96+2513G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65719414 | ||||||
| chrX:65719535
|
T | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+2634T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65719535 | ||||||
| chrX:65719557
|
A | AG | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.96+2659dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65719557 | |||||
| chrX:65719641
|
A | AG | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.96+2743dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65719641 | |||||
| chrX:65719648
|
C | CG | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.96+2749dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65719648 | |||||
| chrX:65719819
|
G | GC | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.96+2919dupC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65719819 | |||||
| chrX:65719836
|
A | AG | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.96+2937dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65719836 | |||||
| chrX:65719856
|
T | TG | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.96+2960dupG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65719856 | |||||
| chrX:65719924
|
T | C | 4 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0010g0040others(1): Show | 4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+3023T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65719924 | ||||||
| chrX:65720427
|
G | A | 4 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0010g0040others(1): Show | 4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+3526G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65720427 | ||||||
| chrX:65720456
|
G | A | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+3555G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65720456 | ||||||
| chrX:65720588
|
G | A | 1 | a0001c0001t0003g0050 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+3687G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65720588 | ||||||
| chrX:65721034
|
A | G | 1 | a0001c0001t0001g0003 | 2 | NA18994.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.96+4133A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721034 | ||||||
| chrX:65721188
|
A | T | 51 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(48): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.96+4287A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721188 | ||||||
| chrX:65721233
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.96+4332A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721233 | ||||||
| chrX:65721312
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96+4411C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721312 | ||||||
| chrX:65721519
|
C | CT | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(24): Show | 32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.96+4620dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65721519 | |||||
| chrX:65721556
|
CT | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0029 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.96+4666delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65721556 | |||||
| chrX:65721772
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.96+4871C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65721772 | ||||||
| chrX:65722401
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0076 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.97-5413G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722401 | ||||||
| chrX:65722404
|
C | CGT | 9 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0122others(6): Show | 9 | HG00738.hp1 HG02135.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-5373_97-5372dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722404
|
C | CGTGT | 14 | a0001c0001t0002g0009a0001c0001t0002g0028a0001c0001t0002g0029others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.97-5375_97-5372dup others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722404
|
C | CGTGTGT | 7 | a0001c0001t0002g0011a0001c0001t0002g0024a0001c0001t0002g0031others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-5377_97-5372dup others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722404
|
C | CGTGTGTG others(1): Show |
15 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(12): Show | 20 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.97-5379_97-5372dup others(8): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722404
|
C | CGTGTGTG others(3): Show |
5 | a0001c0001t0002g0019a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG00735.hp2 HG02109.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-5381_97-5372dup others(10): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722404
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0002g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-5383_97-5372dup others(12): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722404
|
CGT | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0095a0001c0001t0001g0109others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.97-5373_97-5372del others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722404
|
CGTGT | C | 1 | a0001c0001t0001g0153 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.97-5375_97-5372del others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722404
|
CGTGTGT | C | 3 | a0001c0001t0001g0154a0001c0001t0002g0014a0002c0002t0001g0155 | 3 | HG02809.hp1 NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.97-5377_97-5372del others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722404 | |||||
| chrX:65722441
|
GT | G | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.97-5370delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65722441 | |||||
| chrX:65722463
|
C | T | 2 | a0001c0001t0006g0016a0001c0001t0006g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.97-5351C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722463 | ||||||
| chrX:65722509
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0103a0001c0001t0001g0135 | 3 | HG02015.hp1 HG02074.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.97-5305G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722509 | ||||||
| chrX:65722666
|
C | T | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(23): Show | 31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.97-5148C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722666 | ||||||
| chrX:65722695
|
C | T | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(24): Show | 32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-5119C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722695 | ||||||
| chrX:65722857
|
T | C | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(24): Show | 32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-4957T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65722857 | ||||||
| chrX:65723082
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.97-4732C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723082 | ||||||
| chrX:65723164
|
T | C | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-4650T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723164 | ||||||
| chrX:65723208
|
T | C | 25 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(22): Show | 30 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.97-4606T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723208 | ||||||
| chrX:65723272
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0115 | 3 | HG02602.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.97-4542A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723272 | ||||||
| chrX:65723384
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | HG00738.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.97-4430C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723384 | ||||||
| chrX:65723718
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97-4096A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723718 | ||||||
| chrX:65723817
|
C | G | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(24): Show | 32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-3997C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723817 | ||||||
| chrX:65723900
|
G | A | 1 | a0001c0001t0010g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-3914G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65723900 | ||||||
| chrX:65724038
|
C | CT | 2 | a0001c0001t0002g0044a0001c0001t0011g0043 | 2 | HG01081.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.97-3763dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65724038 | |||||
| chrX:65724038
|
CT | C | 2 | a0001c0001t0001g0158a0001c0001t0002g0011 | 2 | HG01515.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.97-3763delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65724038 | |||||
| chrX:65724122
|
C | T | 4 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0010g0040others(1): Show | 4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-3692C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724122 | ||||||
| chrX:65724147
|
C | CT | 4 | a0001c0001t0002g0041a0001c0001t0002g0044a0001c0001t0010g0040others(1): Show | 4 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-3653dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65724147 | |||||
| chrX:65724206
|
G | A | 1 | a0001c0001t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.97-3608G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724206 | ||||||
| chrX:65724307
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97-3507G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724307 | ||||||
| chrX:65724391
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.97-3423G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724391 | ||||||
| chrX:65724677
|
T | TTTTG | 44 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(41): Show | 49 | HG00735.hp2 HG00738.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.97-3113_97-3110dup others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65724677 | |||||
| chrX:65724677
|
TTTTG | T | 3 | a0001c0001t0001g0054a0001c0001t0002g0044a0001c0001t0011g0043 | 3 | HG01081.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.97-3113_97-3110del others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chrX | 65724677 | |||||
| chrX:65724721
|
C | T | 1 | a0001c0001t0008g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97-3093C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724721 | ||||||
| chrX:65724777
|
C | G | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.97-3037C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724777 | ||||||
| chrX:65724780
|
A | G | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(24): Show | 32 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.97-3034A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724780 | ||||||
| chrX:65724847
|
C | T | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-2967C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724847 | ||||||
| chrX:65724978
|
C | T | 1 | a0001c0001t0011g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.97-2836C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65724978 | ||||||
| chrX:65725244
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.97-2570C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65725244 | ||||||
| chrX:65725647
|
A | C | 1 | a0001c0001t0010g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-2167A>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65725647 | ||||||
| chrX:65725784
|
C | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0140 | 2 | HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.97-2030C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65725784 | ||||||
| chrX:65726122
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0115 | 3 | HG02602.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.97-1692A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65726122 | ||||||
| chrX:65726469
|
T | G | 19 | a0001c0001t0001g0007a0001c0001t0001g0064a0001c0001t0001g0067others(16): Show | 19 | HG01069.hp1 HG01256.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.97-1345T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65726469 | ||||||
| chrX:65726569
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.97-1245T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65726569 | ||||||
| chrX:65726854
|
TC | T | 1 | a0001c0001t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.97-959delC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65726854 | ||||||
| chrX:65727365
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-449G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65727365 | ||||||
| chrX:65727709
|
C | A | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-105C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65727709 | ||||||
| chrX:65727758
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.97-56C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 2/12 | chrX | 65727758 | ||||||
| chrX:65727978
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.192+69T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65727978 | ||||||
| chrX:65728127
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0108others(1): Show | 4 | NA18960.hp1 NA19000.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+218G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65728127 | ||||||
| chrX:65728209
|
TG | T | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.192+302delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 65728209 | |||||
| chrX:65728285
|
TTTG | T | 1 | a0001c0001t0006g0016 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.192+379_192+381del others(3): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 65728285 | |||||
| chrX:65728336
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.192+427C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65728336 | ||||||
| chrX:65728630
|
GA | G | 6 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(3): Show | 6 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+732delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chrX | 65728630 | |||||
| chrX:65728662
|
T | G | 7 | a0001c0001t0002g0014a0001c0001t0002g0041a0001c0001t0002g0044others(4): Show | 7 | HG01081.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+753T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65728662 | ||||||
| chrX:65728828
|
C | T | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(23): Show | 31 | HG01243.hp1 HG02109.hp2 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-610C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65728828 | ||||||
| chrX:65729141
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.193-297A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 3/12 | chrX | 65729141 | ||||||
| chrX:65729995
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.467+283T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65729995 | ||||||
| chrX:65730029
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.467+317T>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730029 | ||||||
| chrX:65730039
|
T | C | 1 | a0001c0001t0002g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.467+327T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730039 | ||||||
| chrX:65730117
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0096 | 2 | HG02040.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.467+405G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730117 | ||||||
| chrX:65730128
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.467+416T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730128 | ||||||
| chrX:65730262
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.467+550G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730262 | ||||||
| chrX:65730384
|
C | T | 1 | a0001c0001t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.467+672C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 4/12 | chrX | 65730384 | ||||||
| chrX:65731212
|
T | C | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.551+22T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 5/12 | chrX | 65731212 | ||||||
| chrX:65732980
|
G | T | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.699-204G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 6/12 | chrX | 65732980 | ||||||
| chrX:65733060
|
T | TA | 3 | a0001c0001t0001g0063a0001c0001t0001g0127a0001c0001t0012g0015 | 3 | HG03471.hp1 HG04228.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.699-111dupA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 65733060 | |||||
| chrX:65733060
|
TA | T | 1 | a0001c0001t0007g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.699-111delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 65733060 | |||||
| chrX:65733076
|
G | A | 4 | a0001c0001t0001g0081a0001c0001t0001g0084a0001c0001t0001g0115others(1): Show | 4 | HG02602.hp1 HG02735.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.699-108G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 6/12 | chrX | 65733076 | ||||||
| chrX:65733430
|
T | C | 7 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0019others(4): Show | 8 | HG02717.hp1 HG02886.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+150T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733430 | ||||||
| chrX:65733535
|
AG | A | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.795+257delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65733535 | |||||
| chrX:65733676
|
C | CCT | 5 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0108others(2): Show | 5 | HG02809.hp1 NA18960.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.795+413_795+414dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65733676 | |||||
| chrX:65733676
|
CCTCT | C | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.795+411_795+414del others(4): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65733676 | |||||
| chrX:65733813
|
C | G | 1 | a0001c0001t0004g0056 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.795+533C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733813 | ||||||
| chrX:65733863
|
G | A | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(46): Show | 54 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.795+583G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733863 | ||||||
| chrX:65733892
|
G | A | 4 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0126others(1): Show | 4 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+612G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733892 | ||||||
| chrX:65733917
|
G | T | 7 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0019others(4): Show | 8 | HG02717.hp1 HG02886.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+637G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65733917 | ||||||
| chrX:65733962
|
C | CT | 37 | a0001c0001t0001g0151a0001c0001t0002g0001a0001c0001t0002g0002others(34): Show | 42 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.795+692dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65733962 | |||||
| chrX:65733962
|
C | CTT | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.795+691_795+692dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65733962 | |||||
| chrX:65734011
|
A | G | 1 | a0001c0001t0004g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.795+731A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65734011 | ||||||
| chrX:65734382
|
GT | G | 1 | a0001c0001t0002g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.796-884delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65734382 | ||||||
| chrX:65734522
|
G | A | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.796-745G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65734522 | ||||||
| chrX:65734612
|
T | TTC | 1 | a0001c0001t0001g0151 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.796-653_796-652dup others(2): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65734612 | |||||
| chrX:65734690
|
AG | A | 1 | a0001c0001t0001g0151 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.796-574delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65734690 | |||||
| chrX:65734701
|
TA | T | 1 | a0001c0001t0001g0151 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.796-561delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65734701 | |||||
| chrX:65734866
|
AT | A | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.796-399delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65734866 | |||||
| chrX:65734996
|
G | T | 1 | a0001c0001t0002g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.796-271G>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65734996 | ||||||
| chrX:65735015
|
CA | C | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.796-249delA | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65735015 | |||||
| chrX:65735044
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.796-223A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65735044 | ||||||
| chrX:65735197
|
CT | C | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.796-66delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chrX | 65735197 | |||||
| chrX:65735231
|
C | CT | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.796-36_796-35insT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 7/12 | chrX | 65735231 | ||||||
| chrX:65735560
|
C | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+130C>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65735560 | ||||||
| chrX:65735698
|
A | G | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+268A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65735698 | ||||||
| chrX:65735842
|
A | G | 1 | a0001c0001t0012g0015 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.959+412A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65735842 | ||||||
| chrX:65735906
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.959+476C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65735906 | ||||||
| chrX:65736096
|
G | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+666G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736096 | ||||||
| chrX:65736134
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA18970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.960-661A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736134 | ||||||
| chrX:65736139
|
C | A | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.960-656C>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736139 | ||||||
| chrX:65736307
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.960-488C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736307 | ||||||
| chrX:65736437
|
C | CT | 6 | a0001c0001t0001g0113a0001c0001t0001g0145a0001c0001t0002g0041others(3): Show | 6 | HG01081.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.960-342dupT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 65736437 | |||||
| chrX:65736437
|
CT | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0064a0001c0001t0002g0001others(30): Show | 38 | HG01243.hp1 HG01256.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.960-342delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 65736437 | |||||
| chrX:65736451
|
T | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(2): Show | 5 | HG00738.hp1 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.960-344T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736451 | ||||||
| chrX:65736474
|
G | GC | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.960-318dupC | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 65736474 | |||||
| chrX:65736598
|
C | T | 2 | a0001c0001t0007g0038a0001c0001t0007g0039 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.960-197C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736598 | ||||||
| chrX:65736640
|
G | C | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.960-155G>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736640 | ||||||
| chrX:65736749
|
G | A | 39 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(36): Show | 44 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.960-46G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 8/12 | chrX | 65736749 | ||||||
| chrX:65737426
|
TG | T | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1251+90delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 65737426 | |||||
| chrX:65737711
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1251+373A>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65737711 | ||||||
| chrX:65737807
|
AACCC | A | 51 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(48): Show | 56 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1251+475_1251+478d others(6): Show |
MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 65737807 | |||||
| chrX:65737892
|
TG | T | 1 | a0002c0002t0001g0155 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1251+556delG | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 65737892 | |||||
| chrX:65737926
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1251+588T>C | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65737926 | ||||||
| chrX:65738004
|
T | A | 1 | a0001c0001t0001g0146 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1252-521T>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738004 | ||||||
| chrX:65738072
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1252-453C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738072 | ||||||
| chrX:65738228
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0148 | 2 | NA18953.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1252-297C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738228 | ||||||
| chrX:65738396
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1252-129G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738396 | ||||||
| chrX:65738521
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.1252-4G>A | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 10/12 | chrX | 65738521 | ||||||
| chrX:65738631
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1344+14C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 11/12 | chrX | 65738631 | ||||||
| chrX:65738731
|
C | T | 5 | a0001c0001t0004g0047a0001c0001t0004g0056a0001c0001t0004g0125others(2): Show | 5 | HG00735.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1344+114C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 11/12 | chrX | 65738731 | ||||||
| chrX:65738894
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0135 | 2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1345-76C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 11/12 | chrX | 65738894 | ||||||
| chrX:65739543
|
AT | A | 10 | a0001c0001t0003g0006a0001c0001t0003g0048a0001c0001t0003g0049others(7): Show | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1570-177delT | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 65739543 | |||||
| chrX:65739703
|
C | T | 2 | a0001c0001t0002g0031a0001c0001t0002g0034 | 2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1570-26C>T | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 12/12 | chrX | 65739703 | ||||||
| chrX:65739715
|
A | G | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(34): Show | 42 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.1570-14A>G | MSN | ENSG00000147065.18 | transcript | ENST00000360270.7 | protein_coding | 12/12 | chrX | 65739715 |