geneid | 139322 |
---|---|
ensemblid | ENSG00000155008.16 |
hgncid | 24009 |
symbol | APOOL |
name | apolipoprotein O like |
refseq_nuc | NM_198450.6 |
refseq_prot | NP_940852.3 |
ensembl_nuc | ENST00000373173.7 |
ensembl_prot | ENSP00000362268.2 |
mane_status | MANE Select |
chr | chrX |
start | 85003877 |
end | 85093315 |
strand | + |
ver | v1.2 |
region | chrX:85003877-85093315 |
region5000 | chrX:84998877-85098315 |
regionname0 | APOOL_chrX_85003877_85093315 |
regionname5000 | APOOL_chrX_84998877_85098315 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5537 | 37 | 0 | 6 | 24 | 1 | 6 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0002 | 0/0 | 5538 | 26 | 0 | 9 | 13 | 1 | 3 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0003 | 0/0 | 5536 | 15 | 2 | 1 | 11 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0004 | 0/0 | 5823 | 9 | 7 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0005 | 0/0 | 5539 | 9 | 0 | 4 | 3 | 1 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0006 | 0/0 | 5823 | 5 | 3 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0007 | 0/0 | 5538 | 5 | 0 | 0 | 5 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0008 | 0/0 | 5540 | 5 | 5 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0009 | 0/0 | 5526 | 4 | 4 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0010 | 0/0 | 5535 | 4 | 4 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0011 | 0/0 | 5525 | 3 | 3 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0012 | 0/0 | 5536 | 3 | 0 | 1 | 0 | 0 | 2 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0013 | 0/0 | 5540 | 3 | 0 | 1 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0014 | 0/0 | 5541 | 3 | 2 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0015 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0016 | 0/0 | 5823 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0017 | 0/0 | 5824 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0018 | 0/0 | 5537 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0019 | 0/0 | 5537 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0020 | 0/0 | 5538 | 2 | 0 | 0 | 0 | 0 | 2 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0021 | 0/0 | 5540 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0022 | 0/0 | 5525 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0023 | 0/0 | 6134 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0024 | 0/0 | 6346 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0025 | 0/0 | 6164 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0026 | 0/0 | 6198 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0027 | 0/0 | 6132 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0028 | 0/1 | 6164 | 2 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0029 | 0/0 | 6198 | 2 | 0 | 0 | 0 | 2 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0030 | 0/0 | 5964 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0031 | 0/0 | 6250 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0032 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0033 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0034 | 0/0 | 5941 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0035 | 0/0 | 6029 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0036 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0037 | 0/0 | 5856 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0038 | 0/0 | 5822 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0039 | 0/0 | 5823 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0040 | 0/0 | 5791 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0041 | 0/0 | 5792 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0042 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0043 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0044 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0045 | 0/0 | 6171 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0046 | 0/0 | 6199 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0047 | 0/0 | 5816 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0048 | 1/0 | 5674 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0049 | 0/0 | 5932 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0050 | 0/0 | 5985 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0051 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0052 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0053 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0054 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0055 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0056 | 0/0 | 5538 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0057 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0058 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0059 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0060 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0061 | 0/0 | 6200 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0062 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0063 | 0/0 | 6076 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0064 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0065 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0066 | 0/0 | 5951 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0067 | 0/0 | 6319 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0068 | 0/0 | 6316 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0069 | 0/0 | 6134 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0070 | 0/0 | 6317 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0071 | 0/0 | 6156 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0072 | 0/0 | 6196 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0073 | 0/0 | 6193 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0074 | 0/0 | 6197 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0075 | 0/0 | 6198 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0076 | 0/0 | 6197 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0077 | 0/0 | 6134 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0078 | 0/0 | 6292 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0079 | 0/0 | 6164 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0080 | 0/0 | 6102 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0081 | 0/0 | 6160 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0082 | 0/0 | 6133 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0083 | 0/0 | 6186 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0084 | 0/0 | 6164 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0085 | 0/0 | 6165 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0086 | 0/0 | 6196 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0087 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0088 | 0/0 | 6133 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0089 | 0/0 | 6162 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0090 | 0/0 | 6132 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0091 | 0/0 | 6196 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0092 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0093 | 0/0 | 6282 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0094 | 0/0 | 6295 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0095 | 0/0 | 6196 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0096 | 0/0 | 6195 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0097 | 0/0 | 6196 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0098 | 0/0 | 6132 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0099 | 0/0 | 6133 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0100 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0101 | 0/0 | 6110 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0102 | 0/0 | 6142 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0103 | 0/0 | 6103 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0104 | 0/0 | 6162 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0105 | 0/0 | 5976 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0106 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0107 | 0/0 | 6317 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0108 | 0/0 | 6061 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0109 | 0/0 | 6071 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0110 | 0/0 | 6037 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0111 | 0/0 | 6006 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0112 | 0/0 | 6129 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0113 | 0/0 | 6190 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0114 | 0/0 | 6065 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0115 | 0/0 | 6104 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0116 | 0/0 | 5910 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0117 | 0/0 | 6196 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0118 | 0/0 | 6291 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0119 | 0/0 | 6319 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0120 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0121 | 0/0 | 6296 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
t0122 | 0/0 | 6318 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 807 | 255 | 72 | 48 | 106 | 7 | 20 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0002c0002 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6343 | 37 | 0 | 6 | 24 | 1 | 6 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0002 | 0/0 | 6344 | 26 | 0 | 9 | 13 | 1 | 3 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0003 | 0/0 | 6342 | 15 | 2 | 1 | 11 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0004 | 0/0 | 6629 | 9 | 7 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0005 | 0/0 | 6345 | 9 | 0 | 4 | 3 | 1 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0006 | 0/0 | 6629 | 5 | 3 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0007 | 0/0 | 6344 | 5 | 0 | 0 | 5 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0008 | 0/0 | 6346 | 5 | 5 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0009 | 0/0 | 6332 | 4 | 4 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0010 | 0/0 | 6341 | 4 | 4 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0011 | 0/0 | 6331 | 3 | 3 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0012 | 0/0 | 6342 | 3 | 0 | 1 | 0 | 0 | 2 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0013 | 0/0 | 6346 | 3 | 0 | 1 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0014 | 0/0 | 6347 | 3 | 2 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0015 | 0/0 | 6656 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0016 | 0/0 | 6629 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0017 | 0/0 | 6630 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0018 | 0/0 | 6343 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0019 | 0/0 | 6343 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0020 | 0/0 | 6344 | 2 | 0 | 0 | 0 | 0 | 2 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0021 | 0/0 | 6346 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0022 | 0/0 | 6331 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0023 | 0/0 | 6940 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0024 | 0/0 | 7152 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0025 | 0/0 | 6970 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0026 | 0/0 | 7004 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0027 | 0/0 | 6938 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0028 | 0/1 | 6970 | 2 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0029 | 0/0 | 7004 | 2 | 0 | 0 | 0 | 2 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0030 | 0/0 | 6770 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0031 | 0/0 | 7056 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0032 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0033 | 0/0 | 6410 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0034 | 0/0 | 6747 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0035 | 0/0 | 6835 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0036 | 0/0 | 6661 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0037 | 0/0 | 6662 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0038 | 0/0 | 6628 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0039 | 0/0 | 6629 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0041 | 0/0 | 6598 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0042 | 0/0 | 6597 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0043 | 0/0 | 6597 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0044 | 0/0 | 6597 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0045 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0046 | 0/0 | 7005 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0047 | 0/0 | 6622 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0048 | 1/0 | 6480 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0049 | 0/0 | 6738 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0050 | 0/0 | 6791 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0051 | 0/0 | 6340 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0052 | 0/0 | 6344 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0053 | 0/0 | 6343 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0054 | 0/0 | 6345 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0055 | 0/0 | 6344 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0056 | 0/0 | 6344 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0057 | 0/0 | 6343 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0058 | 0/0 | 6345 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0059 | 0/0 | 6347 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0060 | 0/0 | 6881 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0061 | 0/0 | 7006 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0062 | 0/0 | 6881 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0063 | 0/0 | 6882 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0064 | 0/0 | 6881 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0065 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0066 | 0/0 | 6757 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0067 | 0/0 | 7125 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0068 | 0/0 | 7122 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0069 | 0/0 | 6940 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0070 | 0/0 | 7123 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0071 | 0/0 | 6962 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0072 | 0/0 | 7002 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0073 | 0/0 | 6999 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0074 | 0/0 | 7003 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0075 | 0/0 | 7004 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0076 | 0/0 | 7003 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0077 | 0/0 | 6940 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0078 | 0/0 | 7098 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0079 | 0/0 | 6970 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0080 | 0/0 | 6908 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0081 | 0/0 | 6966 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0082 | 0/0 | 6939 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0083 | 0/0 | 6992 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0084 | 0/0 | 6970 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0085 | 0/0 | 6971 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0086 | 0/0 | 7002 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0087 | 0/0 | 7033 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0088 | 0/0 | 6939 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0089 | 0/0 | 6968 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0090 | 0/0 | 6938 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0091 | 0/0 | 7002 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0092 | 0/0 | 7120 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0093 | 0/0 | 7088 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0094 | 0/0 | 7101 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0095 | 0/0 | 7002 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0096 | 0/0 | 7001 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0097 | 0/0 | 7002 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0098 | 0/0 | 6938 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0099 | 0/0 | 6939 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0100 | 0/0 | 6887 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0101 | 0/0 | 6916 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0102 | 0/0 | 6948 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0103 | 0/0 | 6909 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0104 | 0/0 | 6968 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0105 | 0/0 | 6782 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0106 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0107 | 0/0 | 7123 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0108 | 0/0 | 6867 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0109 | 0/0 | 6877 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0110 | 0/0 | 6843 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0111 | 0/0 | 6812 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0112 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0113 | 0/0 | 6996 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0114 | 0/0 | 6871 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0115 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0116 | 0/0 | 6716 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0117 | 0/0 | 7002 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0118 | 0/0 | 7097 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0119 | 0/0 | 7125 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0120 | 0/0 | 7120 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0121 | 0/0 | 7102 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0001c0001t0122 | 0/0 | 7124 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
a0002c0002t0040 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | copy fasta | chrX | 84998877 | 85098315 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0010g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0010g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0010g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0011g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0011g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0012g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0012g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0013g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0013g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0013g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0014g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0014g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0014g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0015g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0016g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0016g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0017g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0017g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0018g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0019g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0020g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0020g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0021g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0021g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0022g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0022g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0023g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0023g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0024g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0025g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0025g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0026g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0026g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0027g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0027g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0028g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0028g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0029g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0029g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0030g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0030g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0031g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0031g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0032g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0033g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0034g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0035g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0036g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0037g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0038g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0039g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0041g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0042g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0043g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0044g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0045g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0046g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0047g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0048g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0049g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0050g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0051g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0052g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0053g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0054g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0055g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0056g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0057g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0058g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0059g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0060g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0061g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0062g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0063g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0064g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0065g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0066g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0067g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0068g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0069g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0070g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0071g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0072g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0073g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0074g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0075g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0076g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0077g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0078g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0079g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0080g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0081g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0082g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0083g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0084g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0085g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0086g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0087g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0088g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0089g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0090g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0091g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0092g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0093g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0094g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0095g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0096g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0097g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0098g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0099g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0100g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0101g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0102g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0103g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0104g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0105g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0106g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0107g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0108g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0109g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0110g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0111g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0112g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0113g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0114g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0115g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0116g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0117g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0118g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0119g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0120g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0121g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0001c0001t0122g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
a0002c0002t0040g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0100 | EUR | FIN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00438 | hp1 | a0001 | c0001 | t0107 | g0075 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00558 | hp1 | a0001 | c0001 | t0082 | g0069 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00621 | hp1 | a0001 | c0001 | t0087 | g0045 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00673 | hp1 | a0001 | c0001 | t0023 | g0026 | EAS | CHS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00733 | hp1 | a0001 | c0001 | t0061 | g0071 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00735 | hp1 | a0001 | c0001 | t0103 | g0023 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG00738 | hp1 | a0001 | c0001 | t0041 | g0241 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01069 | hp1 | a0001 | c0001 | t0031 | g0061 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01071 | hp1 | a0001 | c0001 | t0031 | g0003 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01074 | hp1 | a0001 | c0001 | t0025 | g0046 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01081 | hp1 | a0001 | c0001 | t0072 | g0054 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01106 | hp1 | a0001 | c0001 | t0076 | g0031 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0244 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01168 | hp2 | a0001 | c0001 | t0073 | g0053 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0238 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01175 | hp2 | a0001 | c0001 | t0025 | g0049 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01243 | hp1 | a0001 | c0001 | t0014 | g0173 | AMR | PUR | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01255 | hp1 | a0001 | c0001 | t0012 | g0204 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01256 | hp1 | a0001 | c0001 | t0057 | g0114 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01257 | hp1 | a0001 | c0001 | t0024 | g0004 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01258 | hp1 | a0001 | c0001 | t0024 | g0004 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01346 | hp2 | a0001 | c0001 | t0084 | g0017 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01358 | hp1 | a0001 | c0001 | t0075 | g0079 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01361 | hp1 | a0001 | c0001 | t0091 | g0059 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0099 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01515 | hp1 | a0001 | c0001 | t0029 | g0212 | EUR | IBS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01517 | hp1 | a0001 | c0001 | t0054 | g0141 | EUR | IBS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01517 | hp2 | a0001 | c0001 | t0029 | g0213 | EUR | IBS | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0202 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01884 | hp2 | a0001 | c0001 | t0037 | g0223 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01891 | hp1 | a0001 | c0001 | t0055 | g0209 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01891 | hp2 | a0001 | c0001 | t0063 | g0051 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01928 | hp1 | a0001 | c0001 | t0070 | g0081 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0090 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0155 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01978 | hp2 | a0001 | c0001 | t0013 | g0129 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02004 | hp1 | a0001 | c0001 | t0098 | g0156 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02004 | hp2 | a0001 | c0001 | t0068 | g0082 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02015 | hp1 | a0001 | c0001 | t0113 | g0043 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0142 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02040 | hp1 | a0001 | c0001 | t0007 | g0207 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02055 | hp1 | a0001 | c0001 | t0105 | g0217 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02056 | hp1 | a0001 | c0001 | t0013 | g0181 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02071 | hp1 | a0001 | c0001 | t0104 | g0027 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02074 | hp1 | a0001 | c0001 | t0083 | g0039 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02135 | hp1 | a0001 | c0001 | t0090 | g0010 | EAS | KHV | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02145 | hp1 | a0001 | c0001 | t0114 | g0216 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02165 | hp1 | a0001 | c0001 | t0080 | g0070 | EAS | CDX | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | CDX | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02257 | hp1 | a0001 | c0001 | t0022 | g0120 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02257 | hp2 | a0001 | c0001 | t0009 | g0170 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02273 | hp2 | a0001 | c0001 | t0067 | g0083 | AMR | PEL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02280 | hp2 | a0001 | c0001 | t0065 | g0018 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02451 | hp1 | a0002 | c0002 | t0040 | g0237 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02451 | hp2 | a0001 | c0001 | t0019 | g0210 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02602 | hp1 | a0001 | c0001 | t0012 | g0158 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0127 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02615 | hp2 | a0001 | c0001 | t0018 | g0197 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02622 | hp1 | a0001 | c0001 | t0116 | g0073 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02622 | hp2 | a0001 | c0001 | t0078 | g0056 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0199 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02630 | hp2 | a0001 | c0001 | t0034 | g0236 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02647 | hp1 | a0001 | c0001 | t0112 | g0019 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02723 | hp1 | a0001 | c0001 | t0115 | g0215 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02723 | hp2 | a0001 | c0001 | t0064 | g0024 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0119 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02738 | hp1 | a0001 | c0001 | t0052 | g0148 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02809 | hp1 | a0001 | c0001 | t0017 | g0240 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02809 | hp2 | a0001 | c0001 | t0036 | g0225 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02818 | hp1 | a0001 | c0001 | t0047 | g0011 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02818 | hp2 | a0001 | c0001 | t0030 | g0072 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02886 | hp1 | a0001 | c0001 | t0014 | g0201 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02895 | hp1 | a0001 | c0001 | t0016 | g0245 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02897 | hp1 | a0001 | c0001 | t0016 | g0239 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02897 | hp2 | a0001 | c0001 | t0058 | g0084 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02922 | hp1 | a0001 | c0001 | t0010 | g0192 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02922 | hp2 | a0001 | c0001 | t0038 | g0230 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02965 | hp1 | a0001 | c0001 | t0018 | g0168 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0007 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02970 | hp2 | a0001 | c0001 | t0111 | g0052 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0169 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03017 | hp1 | a0001 | c0001 | t0020 | g0203 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03041 | hp1 | a0001 | c0001 | t0108 | g0214 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03041 | hp2 | a0001 | c0001 | t0106 | g0015 | AFR | GWD | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03098 | hp1 | a0001 | c0001 | t0010 | g0094 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0124 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03195 | hp1 | a0001 | c0001 | t0051 | g0006 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03195 | hp2 | a0001 | c0001 | t0022 | g0163 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0108 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0128 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03486 | hp1 | a0001 | c0001 | t0035 | g0219 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0200 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03516 | hp1 | a0001 | c0001 | t0015 | g0007 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03516 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | ESN | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0126 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03688 | hp1 | a0001 | c0001 | t0056 | g0150 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03704 | hp1 | a0001 | c0001 | t0081 | g0062 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03704 | hp2 | a0001 | c0001 | t0020 | g0185 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03710 | hp1 | a0001 | c0001 | t0094 | g0032 | SAS | PJL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03831 | hp1 | a0001 | c0001 | t0046 | g0040 | SAS | BEB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0188 | SAS | STU | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18522 | hp1 | a0001 | c0001 | t0019 | g0208 | AFR | YRI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18906 | hp1 | a0001 | c0001 | t0017 | g0243 | AFR | YRI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | YRI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18948 | hp1 | a0001 | c0001 | t0007 | g0193 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18950 | hp2 | a0001 | c0001 | t0097 | g0060 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18952 | hp1 | a0001 | c0001 | t0042 | g0222 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18953 | hp1 | a0001 | c0001 | t0043 | g0221 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18954 | hp2 | a0001 | c0001 | t0026 | g0078 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18959 | hp1 | a0001 | c0001 | t0079 | g0235 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18962 | hp1 | a0001 | c0001 | t0007 | g0162 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18963 | hp2 | a0001 | c0001 | t0086 | g0034 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18964 | hp2 | a0001 | c0001 | t0077 | g0021 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18965 | hp1 | a0001 | c0001 | t0021 | g0159 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18967 | hp1 | a0001 | c0001 | t0060 | g0022 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18968 | hp1 | a0001 | c0001 | t0039 | g0220 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18969 | hp1 | a0001 | c0001 | t0092 | g0076 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18969 | hp2 | a0001 | c0001 | t0053 | g0152 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18971 | hp1 | a0001 | c0001 | t0089 | g0057 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18975 | hp2 | a0001 | c0001 | t0085 | g0037 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18977 | hp1 | a0001 | c0001 | t0119 | g0033 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18981 | hp1 | a0001 | c0001 | t0050 | g0014 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18982 | hp1 | a0001 | c0001 | t0095 | g0067 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18985 | hp1 | a0001 | c0001 | t0101 | g0029 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18992 | hp1 | a0001 | c0001 | t0096 | g0038 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18993 | hp2 | a0001 | c0001 | t0069 | g0002 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18995 | hp1 | a0001 | c0001 | t0071 | g0002 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18998 | hp2 | a0001 | c0001 | t0122 | g0063 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19000 | hp1 | a0001 | c0001 | t0100 | g0028 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19001 | hp1 | a0001 | c0001 | t0013 | g0195 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19001 | hp2 | a0001 | c0001 | t0027 | g0058 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19006 | hp1 | a0001 | c0001 | t0088 | g0050 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19011 | hp1 | a0001 | c0001 | t0023 | g0064 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19011 | hp2 | a0001 | c0001 | t0044 | g0218 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19030 | hp1 | a0001 | c0001 | t0109 | g0020 | AFR | LWK | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0101 | AFR | LWK | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19043 | hp1 | a0001 | c0001 | t0049 | g0171 | AFR | LWK | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19057 | hp2 | a0001 | c0001 | t0074 | g0065 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19065 | hp2 | a0001 | c0001 | t0118 | g0066 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19066 | hp1 | a0001 | c0001 | t0027 | g0035 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19068 | hp1 | a0001 | c0001 | t0045 | g0044 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19070 | hp1 | a0001 | c0001 | t0028 | g0042 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19074 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19074 | hp2 | a0001 | c0001 | t0102 | g0055 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19086 | hp1 | a0001 | c0001 | t0093 | g0077 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19087 | hp1 | a0001 | c0001 | t0059 | g0194 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19087 | hp2 | a0001 | c0001 | t0121 | g0030 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19088 | hp1 | a0001 | c0001 | t0021 | g0160 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA19091 | hp1 | a0001 | c0001 | t0026 | g0080 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ASW | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0086 | AFR | ASW | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA20752 | hp1 | a0001 | c0001 | t0099 | g0036 | EUR | TSI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0005 | EUR | TSI | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | GIH | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0088 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG01123 | hp2 | a0001 | c0001 | t0117 | g0003 | AMR | CLM | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02109 | hp1 | a0001 | c0001 | t0033 | g0009 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02109 | hp2 | a0001 | c0001 | t0066 | g0047 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02486 | hp1 | a0001 | c0001 | t0011 | g0198 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02559 | hp1 | a0001 | c0001 | t0032 | g0008 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG02559 | hp2 | a0001 | c0001 | t0062 | g0016 | AFR | ACB | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG03471 | hp1 | a0001 | c0001 | t0030 | g0048 | AFR | MSL | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | USA | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
HG06807 | hp2 | a0001 | c0001 | t0110 | g0025 | AFR | USA | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
NA18955 | hp1 | a0001 | c0001 | t0120 | g0041 | EAS | JPT | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0028 | g0068 | REF | REF | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0048 | g0074 | REF | REF | APOOL_chrX_84998877_85098315 | APOOL | chrX | 84998877 | 85098315 |
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:85074095
|
C | G | 1 | a0002 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.584C>G | p.Pro195Arg | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 7/9 | 620/6480 | 584/807 | 195/268 | chrX | 85074095 |
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:85087777
|
G | A | 2 | a0001c0001t0032a0001c0001t0033 | 2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*99G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 99 | chrX | 85087777 | |||||
chrX:85087993
|
CAT | C | 5 | a0001c0001t0118a0001c0001t0119a0001c0001t0120others(2): Show | 5 | NA18955.hp1 NA18977.hp1 NA18998.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*326_*327delAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 326 | INFO_REALIGN_3_PRIME | chrX | 85087993 | ||||
chrX:85088003
|
T | C | 1 | a0001c0001t0015 | 2 | HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*325T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 325 | chrX | 85088003 | |||||
chrX:85088015
|
AATAC | A | 3 | a0001c0001t0015a0001c0001t0030a0001c0001t0116 | 5 | HG02622.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*345_*348delCATA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 345 | INFO_REALIGN_3_PRIME | chrX | 85088015 | ||||
chrX:85088016
|
A | G | 2 | a0001c0001t0031a0001c0001t0117 | 3 | HG01069.hp1 HG01071.hp1 HG01123.hp2 |
3_prime_UTR_variant | MODIFIER | c.*338A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 338 | chrX | 85088016 | |||||
chrX:85088046
|
G | GTATTAAT others(457): Show |
1 | a0001c0001t0045 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372_*373insAATACA others(458): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 373 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTAAT others(485): Show |
1 | a0001c0001t0046 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372_*373insAATACA others(486): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 373 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(455): Show |
1 | a0001c0001t0061 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(456): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(267): Show |
1 | a0001c0001t0065 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(268): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(267): Show |
1 | a0001c0001t0066 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(268): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(605): Show |
1 | a0001c0001t0067 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(606): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(603): Show |
1 | a0001c0001t0068 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(604): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(633): Show |
1 | a0001c0001t0024 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(634): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(603): Show |
1 | a0001c0001t0070 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(604): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(453): Show |
1 | a0001c0001t0071 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(454): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(451): Show |
3 | a0001c0001t0025a0001c0001t0072a0001c0001t0073 | 4 | HG01074.hp1 HG01081.hp1 HG01168.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(481): Show |
1 | a0001c0001t0074 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(482): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(485): Show |
2 | a0001c0001t0026a0001c0001t0075 | 3 | HG01358.hp1 NA18954.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(486): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(483): Show |
1 | a0001c0001t0076 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(484): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(421): Show |
1 | a0001c0001t0079 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(422): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(451): Show |
2 | a0001c0001t0084a0001c0001t0085 | 2 | HG01346.hp2 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(481): Show |
2 | a0001c0001t0086a0001c0001t0087 | 2 | HG00621.hp1 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(482): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(419): Show |
2 | a0001c0001t0027a0001c0001t0088 | 3 | NA19001.hp2 NA19006.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(449): Show |
1 | a0001c0001t0089 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(450): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(419): Show |
1 | a0001c0001t0090 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(483): Show |
1 | a0001c0001t0091 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(484): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(601): Show |
1 | a0001c0001t0092 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(602): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(569): Show |
1 | a0001c0001t0093 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(570): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(581): Show |
1 | a0001c0001t0094 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(582): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(517): Show |
1 | a0001c0001t0118 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(518): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(451): Show |
1 | a0001c0001t0117 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(483): Show |
1 | a0001c0001t0095 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(484): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(451): Show |
1 | a0001c0001t0028 | 2 | NA19070.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(481): Show |
2 | a0001c0001t0096a0001c0001t0097 | 2 | NA18950.hp2 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(482): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(419): Show |
2 | a0001c0001t0098a0001c0001t0099 | 2 | HG02004.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(357): Show |
1 | a0001c0001t0103 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(358): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(417): Show |
1 | a0001c0001t0104 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(418): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(539): Show |
1 | a0001c0001t0107 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(540): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088046
|
G | GTATTTAT others(477): Show |
1 | a0001c0001t0113 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(478): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088046 | ||||
chrX:85088050
|
T | G | 4 | a0001c0001t0030a0001c0001t0034a0001c0001t0035others(1): Show | 5 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*372T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 372 | chrX | 85088050 | |||||
chrX:85088050
|
T | TTATACAT others(473): Show |
1 | a0001c0001t0083 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(474): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088050 | ||||
chrX:85088050
|
T | TTATACAT others(505): Show |
1 | a0001c0001t0031 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(506): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | INFO_REALIGN_3_PRIME | chrX | 85088050 | ||||
chrX:85088051
|
T | A | 13 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(10): Show | 27 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*373T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 373 | chrX | 85088051 | |||||
chrX:85088055
|
C | CATATATA others(183): Show |
1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383_*384insATGTAT others(184): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 384 | INFO_REALIGN_3_PRIME | chrX | 85088055 | ||||
chrX:85088067
|
AATACATA others(81): Show |
A | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | 136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*398_*485delACATAT others(82): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 398 | INFO_REALIGN_3_PRIME | chrX | 85088067 | ||||
chrX:85088071
|
C | CGTATGTA others(279): Show |
1 | a0001c0001t0030 | 2 | HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATGT others(280): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATGTA others(247): Show |
1 | a0001c0001t0116 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATGT others(248): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(341): Show |
2 | a0001c0001t0062a0001c0001t0063 | 2 | HG01891.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(342): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(341): Show |
1 | a0001c0001t0064 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(342): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(431): Show |
1 | a0001c0001t0023 | 2 | HG00673.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(432): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(431): Show |
1 | a0001c0001t0069 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(432): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(431): Show |
1 | a0001c0001t0077 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(432): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(611): Show |
1 | a0001c0001t0078 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(612): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(419): Show |
1 | a0001c0001t0080 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(449): Show |
1 | a0001c0001t0081 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(450): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(451): Show |
1 | a0001c0001t0082 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(452): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(607): Show |
1 | a0001c0001t0120 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(608): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(637): Show |
1 | a0001c0001t0119 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(638): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(615): Show |
1 | a0001c0001t0121 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(616): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(397): Show |
1 | a0001c0001t0100 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(398): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(429): Show |
1 | a0001c0001t0101 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(430): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(461): Show |
1 | a0001c0001t0102 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(462): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(265): Show |
1 | a0001c0001t0105 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(266): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(113): Show |
1 | a0001c0001t0106 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(114): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(637): Show |
1 | a0001c0001t0122 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(638): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(351): Show |
1 | a0001c0001t0108 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(352): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(361): Show |
1 | a0001c0001t0109 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(362): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(359): Show |
1 | a0001c0001t0110 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(360): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(297): Show |
1 | a0001c0001t0111 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(298): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTAA others(419): Show |
1 | a0001c0001t0112 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTA others(420): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTTA others(215): Show |
1 | a0001c0001t0015 | 2 | HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(216): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTTA others(517): Show |
1 | a0001c0001t0029 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(518): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTTA others(355): Show |
1 | a0001c0001t0114 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(356): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088071
|
C | CGTATTTA others(395): Show |
1 | a0001c0001t0115 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*394insGTATTT others(396): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088071 | |||||
chrX:85088072
|
A | G | 20 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(17): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088072 | |||||
chrX:85088072
|
A | T | 29 | a0001c0001t0015a0001c0001t0023a0001c0001t0029others(26): Show | 33 | HG00558.hp1 HG00673.hp1 HG01515.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 394 | chrX | 85088072 | |||||
chrX:85088073
|
T | TATTA | 20 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(17): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*397_*398insTAAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 398 | INFO_REALIGN_3_PRIME | chrX | 85088073 | ||||
chrX:85088075
|
T | C | 1 | a0001c0001t0106 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 397 | chrX | 85088075 | |||||
chrX:85088077
|
C | T | 1 | a0001c0001t0106 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 399 | chrX | 85088077 | |||||
chrX:85088085
|
TATAA | T | 1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411_*414delAATA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 411 | INFO_REALIGN_3_PRIME | chrX | 85088085 | ||||
chrX:85088093
|
CAT | C | 26 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(23): Show | 42 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*420delTA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088093 | ||||
chrX:85088095
|
T | TACATATT others(263): Show |
1 | a0001c0001t0049 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418_*419insCATATT others(264): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088095 | ||||
chrX:85088095
|
T | TACATATT others(387): Show |
1 | a0001c0001t0060 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418_*419insCATATT others(388): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088095 | ||||
chrX:85088095
|
T | TACATATT others(195): Show |
1 | a0001c0001t0034 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418_*419insCATATT others(196): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088095 | ||||
chrX:85088095
|
T | TACATATT others(255): Show |
1 | a0001c0001t0035 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*418_*419insCATATT others(256): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 419 | INFO_REALIGN_3_PRIME | chrX | 85088095 | ||||
chrX:85088100
|
A | G | 2 | a0001c0001t0032a0001c0001t0033 | 2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*422A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 422 | chrX | 85088100 | |||||
chrX:85088104
|
T | TA | 1 | a0001c0001t0086 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426_*427insA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 427 | chrX | 85088104 | |||||
chrX:85088104
|
T | TTATACAT others(15): Show |
2 | a0001c0001t0069a0001c0001t0071 | 2 | NA18993.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*429_*450dupTACATA others(16): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088104 | ||||
chrX:85088109
|
C | CAT | 18 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(15): Show | 32 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437dupAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 438 | INFO_REALIGN_3_PRIME | chrX | 85088109 | ||||
chrX:85088125
|
C | CAT | 11 | a0001c0001t0015a0001c0001t0030a0001c0001t0069others(8): Show | 13 | HG02055.hp1 HG02145.hp1 HG02622.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*449_*450dupTA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088125 | ||||
chrX:85088125
|
C | CATATACA others(17): Show |
3 | a0001c0001t0023a0001c0001t0077a0001c0001t0108 | 4 | HG00673.hp1 HG03041.hp1 NA18964.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451insTACATA others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088125 | ||||
chrX:85088125
|
C | CATATACA others(49): Show |
3 | a0001c0001t0062a0001c0001t0063a0001c0001t0064 | 3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*450_*451insTACATA others(50): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088125 | ||||
chrX:85088126
|
ATACATAT others(1): Show |
A | 2 | a0001c0001t0106a0001c0001t0110 | 2 | HG03041.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*451_*458delCATATT others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | INFO_REALIGN_3_PRIME | chrX | 85088126 | ||||
chrX:85088129
|
C | A | 1 | a0001c0001t0103 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*451C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 451 | chrX | 85088129 | |||||
chrX:85088130
|
A | G | 4 | a0001c0001t0032a0001c0001t0033a0001c0001t0050others(1): Show | 4 | HG02109.hp1 HG02559.hp1 NA18981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*452A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 452 | chrX | 85088130 | |||||
chrX:85088134
|
T | TTATACAT others(17): Show |
1 | a0001c0001t0049 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467_*468insATGTAT others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 468 | INFO_REALIGN_3_PRIME | chrX | 85088134 | ||||
chrX:85088139
|
C | CAT | 19 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(16): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*466_*467dupAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 468 | INFO_REALIGN_3_PRIME | chrX | 85088139 | ||||
chrX:85088141
|
TATATGTA others(21): Show |
T | 2 | a0001c0001t0032a0001c0001t0033 | 2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*468_*495delGTATAA others(22): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 468 | INFO_REALIGN_3_PRIME | chrX | 85088141 | ||||
chrX:85088155
|
C | CAT | 4 | a0001c0001t0015a0001c0001t0049a0001c0001t0106others(1): Show | 5 | HG02970.hp1 HG03041.hp2 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*479_*480dupTA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATACATA others(219): Show |
2 | a0001c0001t0036a0001c0001t0037 | 2 | HG01884.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(220): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATACATA others(187): Show |
6 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(3): Show | 20 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(188): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATACATA others(155): Show |
2 | a0001c0001t0041a0002c0002t0040 | 2 | HG00738.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(156): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATACATA others(155): Show |
1 | a0001c0001t0042 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(156): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATACATA others(155): Show |
1 | a0001c0001t0043 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(156): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATACATA others(155): Show |
1 | a0001c0001t0044 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(156): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATATACA others(17): Show |
6 | a0001c0001t0105a0001c0001t0109a0001c0001t0111others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*480_*481insTACATA others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATATACA others(39): Show |
1 | a0001c0001t0116 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480_*481insTACATA others(40): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATATACA others(61): Show |
1 | a0001c0001t0030 | 2 | HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*480_*481insTACATA others(62): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088155
|
C | CATATTTA others(339): Show |
1 | a0001c0001t0050 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480_*481insTTTATA others(340): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 481 | INFO_REALIGN_3_PRIME | chrX | 85088155 | ||||
chrX:85088160
|
A | G | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*482A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 482 | chrX | 85088160 | |||||
chrX:85088165
|
T | A | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | 136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*487T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 487 | chrX | 85088165 | |||||
chrX:85088169
|
C | CAT | 17 | a0001c0001t0029a0001c0001t0034a0001c0001t0035others(14): Show | 18 | HG00558.hp1 HG01515.hp1 HG01517.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*496_*497dupAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088169 | ||||
chrX:85088169
|
C | CATATATA others(59): Show |
1 | a0001c0001t0031 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(60): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088169 | ||||
chrX:85088169
|
C | CATATATA others(23): Show |
1 | a0001c0001t0120 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insATGTAT others(24): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chrX | 85088169 | ||||
chrX:85088169
|
C | CATATATG others(25): Show |
31 | a0001c0001t0024a0001c0001t0025a0001c0001t0026others(28): Show | 36 | HG01074.hp1 HG01106.hp1 HG01175.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*527_*558dupTATGTA others(26): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 559 | INFO_REALIGN_3_PRIME | chrX | 85088169 | ||||
chrX:85088169
|
C | CATATATG others(57): Show |
6 | a0001c0001t0061a0001c0001t0072a0001c0001t0087others(3): Show | 6 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*495_*558dupTATGTA others(58): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 559 | INFO_REALIGN_3_PRIME | chrX | 85088169 | ||||
chrX:85088169
|
C | CATATATG others(89): Show |
1 | a0001c0001t0107 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558_*559insTATGTA others(90): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 559 | INFO_REALIGN_3_PRIME | chrX | 85088169 | ||||
chrX:85088169
|
C | CATATATG others(55): Show |
2 | a0001c0001t0073a0001c0001t0079 | 2 | HG01168.hp2 NA18959.hp1 |
3_prime_UTR_variant | MODIFIER | c.*527_*528insGTATAA others(56): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 528 | INFO_REALIGN_3_PRIME | chrX | 85088169 | ||||
chrX:85088169
|
C | CATATATG others(87): Show |
1 | a0001c0001t0118 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527_*528insGTATAA others(88): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 528 | INFO_REALIGN_3_PRIME | chrX | 85088169 | ||||
chrX:85088181
|
AATAC | A | 3 | a0001c0001t0062a0001c0001t0063a0001c0001t0064 | 3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*511_*514delCATA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 511 | INFO_REALIGN_3_PRIME | chrX | 85088181 | ||||
chrX:85088185
|
C | CAT | 1 | a0001c0001t0015 | 2 | HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*509_*510dupTA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 511 | INFO_REALIGN_3_PRIME | chrX | 85088185 | ||||
chrX:85088190
|
A | ATATTTAT others(99): Show |
1 | a0001c0001t0034 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542_*543insTACATA others(100): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 543 | INFO_REALIGN_3_PRIME | chrX | 85088190 | ||||
chrX:85088190
|
A | ATATTTAT others(127): Show |
1 | a0001c0001t0035 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*542_*543insTACATA others(128): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 543 | INFO_REALIGN_3_PRIME | chrX | 85088190 | ||||
chrX:85088190
|
A | G | 3 | a0001c0001t0032a0001c0001t0033a0001c0001t0121 | 3 | HG02109.hp1 HG02559.hp1 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*512A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 512 | chrX | 85088190 | |||||
chrX:85088199
|
CAT | C | 7 | a0001c0001t0015a0001c0001t0023a0001c0001t0030others(4): Show | 10 | HG00673.hp1 HG02622.hp1 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*528_*529delAT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 528 | INFO_REALIGN_3_PRIME | chrX | 85088199 | ||||
chrX:85088206
|
A | G | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | 136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*528A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 528 | chrX | 85088206 | |||||
chrX:85088207
|
TGTATAA | T | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | 136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*530_*535delGTATAA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 530 | chrX | 85088207 | |||||
chrX:85088222
|
A | G | 3 | a0001c0001t0022a0001c0001t0032a0001c0001t0033 | 4 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*544A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 544 | chrX | 85088222 | |||||
chrX:85088316
|
G | GT | 22 | a0001c0001t0038a0001c0001t0045a0001c0001t0046others(19): Show | 22 | HG00438.hp1 HG00735.hp1 HG01106.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*667dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
G | GTT | 19 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(16): Show | 32 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*666_*667dupTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
G | GTTT | 10 | a0001c0001t0010a0001c0001t0017a0001c0001t0037others(7): Show | 14 | HG00738.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*665_*667dupTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
G | GTTTT | 2 | a0001c0001t0003a0001c0001t0049 | 16 | HG01099.hp1 HG02165.hp2 HG03139.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*664_*667dupTTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
G | GTTTTT | 5 | a0001c0001t0001a0001c0001t0018a0001c0001t0019others(2): Show | 43 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*663_*667dupTTTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
G | GTTTTTT | 8 | a0001c0001t0002a0001c0001t0007a0001c0001t0012others(5): Show | 40 | HG00280.hp1 HG00735.hp2 HG01168.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*667dupTTTTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
G | GTTTTTTT | 2 | a0001c0001t0005a0001c0001t0058 | 10 | HG00609.hp1 HG01123.hp1 HG01361.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*661_*667dupTTTTTT others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
G | GTTTTTTT others(1): Show |
4 | a0001c0001t0008a0001c0001t0013a0001c0001t0021others(1): Show | 11 | HG01884.hp1 HG01978.hp2 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*660_*667dupTTTTTT others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
G | GTTTTTTT others(2): Show |
2 | a0001c0001t0014a0001c0001t0050 | 4 | HG01243.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*659_*667dupTTTTTT others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
GT | G | 2 | a0001c0001t0073a0001c0001t0082 | 2 | HG00558.hp1 HG01168.hp2 |
3_prime_UTR_variant | MODIFIER | c.*667delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 667 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
GTTTTTT | G | 1 | a0001c0001t0009 | 4 | HG02257.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*667delTTTTTT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 662 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
GTTTTTTT | G | 2 | a0001c0001t0011a0001c0001t0022 | 5 | HG02257.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*661_*667delTTTTTT others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 661 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088316
|
GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0030a0001c0001t0116 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*656_*667delTTTTTT others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 656 | INFO_REALIGN_3_PRIME | chrX | 85088316 | ||||
chrX:85088345
|
T | TTC | 1 | a0001c0001t0015 | 2 | HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*667_*668insTC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 668 | chrX | 85088345 | |||||
chrX:85088366
|
TA | T | 1 | a0001c0001t0086 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*692delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 692 | INFO_REALIGN_3_PRIME | chrX | 85088366 | ||||
chrX:85088657
|
TC | T | 1 | a0001c0001t0086 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*982delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 982 | INFO_REALIGN_3_PRIME | chrX | 85088657 | ||||
chrX:85088710
|
T | TC | 1 | a0001c0001t0086 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1037dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1038 | INFO_REALIGN_3_PRIME | chrX | 85088710 | ||||
chrX:85088799
|
C | CT | 1 | a0001c0001t0086 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1123dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1124 | INFO_REALIGN_3_PRIME | chrX | 85088799 | ||||
chrX:85088817
|
CAGTGAGC others(42): Show |
C | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 175 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1140_*1188delAGTG others(45): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1140 | chrX | 85088817 | |||||
chrX:85088890
|
A | G | 3 | a0001c0001t0042a0001c0001t0043a0001c0001t0044 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1212A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1212 | chrX | 85088890 | |||||
chrX:85088937
|
CA | C | 1 | a0001c0001t0086 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1264 | INFO_REALIGN_3_PRIME | chrX | 85088937 | ||||
chrX:85088988
|
C | T | 2 | a0001c0001t0030a0001c0001t0116 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1310C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1310 | chrX | 85088988 | |||||
chrX:85089148
|
C | T | 1 | a0001c0001t0081 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1470C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1470 | chrX | 85089148 | |||||
chrX:85089243
|
A | G | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1565A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1565 | chrX | 85089243 | |||||
chrX:85089349
|
C | T | 1 | a0001c0001t0045 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1671 | chrX | 85089349 | |||||
chrX:85089658
|
C | T | 3 | a0001c0001t0004a0001c0001t0036a0001c0001t0038 | 11 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1980C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 1980 | chrX | 85089658 | |||||
chrX:85089713
|
A | T | 1 | a0001c0001t0016 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2035A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2035 | chrX | 85089713 | |||||
chrX:85089732
|
A | G | 19 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(16): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2054A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2054 | chrX | 85089732 | |||||
chrX:85089757
|
GTC | G | 1 | a0001c0001t0012 | 3 | HG01255.hp1 HG02602.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2083_*2084delCT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2083 | INFO_REALIGN_3_PRIME | chrX | 85089757 | ||||
chrX:85089765
|
C | T | 1 | a0001c0001t0117 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2087 | chrX | 85089765 | |||||
chrX:85089966
|
C | CA | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | 148 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*2303dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2304 | INFO_REALIGN_3_PRIME | chrX | 85089966 | ||||
chrX:85089966
|
C | CAA | 3 | a0001c0001t0052a0001c0001t0054a0001c0001t0059 | 3 | HG01517.hp1 HG02738.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2302_*2303dupAA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2304 | INFO_REALIGN_3_PRIME | chrX | 85089966 | ||||
chrX:85090053
|
A | G | 1 | a0001c0001t0026 | 2 | NA18954.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2375A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2375 | chrX | 85090053 | |||||
chrX:85090416
|
ATTC | A | 1 | a0001c0001t0035 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2743_*2745delTCT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 2743 | INFO_REALIGN_3_PRIME | chrX | 85090416 | ||||
chrX:85090702
|
C | T | 2 | a0001c0001t0030a0001c0001t0116 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3024C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3024 | chrX | 85090702 | |||||
chrX:85090859
|
G | C | 5 | a0001c0001t0006a0001c0001t0016a0001c0001t0017others(2): Show | 11 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3181G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3181 | chrX | 85090859 | |||||
chrX:85091058
|
A | G | 1 | a0001c0001t0053 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3380A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3380 | chrX | 85091058 | |||||
chrX:85091205
|
G | A | 1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3527G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3527 | chrX | 85091205 | |||||
chrX:85091282
|
A | G | 1 | a0001c0001t0056 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3604A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3604 | chrX | 85091282 | |||||
chrX:85091445
|
A | G | 1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3767A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3767 | chrX | 85091445 | |||||
chrX:85091474
|
T | C | 3 | a0001c0001t0008a0001c0001t0014a0001c0001t0058 | 9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3796T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3796 | chrX | 85091474 | |||||
chrX:85091529
|
A | AG | 1 | a0001c0001t0035 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3853dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3854 | INFO_REALIGN_3_PRIME | chrX | 85091529 | ||||
chrX:85091603
|
C | T | 1 | a0001c0001t0105 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3925C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3925 | chrX | 85091603 | |||||
chrX:85091623
|
A | T | 21 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(18): Show | 36 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3945A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 3945 | chrX | 85091623 | |||||
chrX:85091727
|
C | G | 3 | a0001c0001t0007a0001c0001t0021a0001c0001t0059 | 8 | HG02040.hp1 NA18948.hp1 NA18954.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4049C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4049 | chrX | 85091727 | |||||
chrX:85091810
|
A | G | 1 | a0001c0001t0015 | 2 | HG02970.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4132A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4132 | chrX | 85091810 | |||||
chrX:85091909
|
T | TA | 1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4240dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4241 | INFO_REALIGN_3_PRIME | chrX | 85091909 | ||||
chrX:85091909
|
TA | T | 1 | a0001c0001t0035 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4240delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4240 | INFO_REALIGN_3_PRIME | chrX | 85091909 | ||||
chrX:85091919
|
T | G | 17 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*4241T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4241 | chrX | 85091919 | |||||
chrX:85091964
|
T | G | 1 | a0001c0001t0018 | 2 | HG02615.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4286T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4286 | chrX | 85091964 | |||||
chrX:85092348
|
A | G | 1 | a0001c0001t0033 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4670A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 4670 | chrX | 85092348 | |||||
chrX:85092892
|
CTG | C | 1 | a0001c0001t0106 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5218_*5219delGT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 5218 | INFO_REALIGN_3_PRIME | chrX | 85092892 | ||||
chrX:85093005
|
A | G | 1 | a0001c0001t0020 | 2 | HG03017.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5327A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 5327 | chrX | 85093005 | |||||
chrX:85093129
|
ATATT | A | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0016others(11): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5456_*5459delTATT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 9/9 | 5456 | INFO_REALIGN_3_PRIME | chrX | 85093129 |
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:85004088
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.15+161C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004088 | ||||||
chrX:85004261
|
AAT | A | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.15+344_15+345delTA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85004261 | |||||
chrX:85004342
|
T | TG | 1 | a0001c0001t0090g0010 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.15+419dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85004342 | |||||
chrX:85004582
|
G | T | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+655G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004582 | ||||||
chrX:85004693
|
T | C | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+766T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004693 | ||||||
chrX:85004771
|
C | T | 12 | a0001c0001t0006g0238a0001c0001t0006g0242a0001c0001t0006g0244others(9): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+844C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004771 | ||||||
chrX:85004808
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.15+881C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004808 | ||||||
chrX:85004845
|
C | T | 1 | a0001c0001t0079g0235 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.15+918C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85004845 | ||||||
chrX:85005020
|
T | C | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+1093T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005020 | ||||||
chrX:85005144
|
A | ATTTTATT | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+1228_15+1234dup others(7): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005144 | |||||
chrX:85005184
|
C | T | 2 | a0001c0001t0029g0212a0001c0001t0029g0213 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.15+1257C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005184 | ||||||
chrX:85005289
|
G | A | 12 | a0001c0001t0006g0238a0001c0001t0006g0242a0001c0001t0006g0244others(9): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+1362G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005289 | ||||||
chrX:85005372
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+1445C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005372 | ||||||
chrX:85005394
|
A | AC | 62 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(59): Show | 62 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+1482dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACC | 56 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(53): Show | 57 | HG00438.hp2 HG00735.hp1 HG01169.hp2 others(54): Show |
intron_variant | MODIFIER | c.15+1481_15+1482dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACCC | 24 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(21): Show | 24 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.15+1480_15+1482dup others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACCCC | 15 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0001g0248others(12): Show | 15 | HG00280.hp1 HG01071.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.15+1479_15+1482dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACCCCC | 5 | a0001c0001t0002g0087a0001c0001t0002g0089a0001c0001t0005g0088others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+1478_15+1482dup others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACCCCCC | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+1477_15+1482dup others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACG | 17 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(14): Show | 17 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.15+1468_15+1469ins others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGC | 5 | a0001c0001t0006g0238a0001c0001t0016g0239a0001c0001t0017g0240others(2): Show | 5 | HG00738.hp1 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+1468_15+1469ins others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGCC | 1 | a0002c0002t0040g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGCCC | 3 | a0001c0001t0039g0220a0001c0001t0042g0222a0001c0001t0043g0221 | 3 | NA18952.hp1 NA18953.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.15+1468_15+1469ins others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGCCCCC | 2 | a0001c0001t0035g0219a0001c0001t0044g0218 | 2 | HG03486.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.15+1468_15+1469ins others(7): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGCCCCC others(1): Show |
1 | a0001c0001t0034g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(8): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGCCCCC others(3): Show |
1 | a0001c0001t0105g0217 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGCCCCC others(4): Show |
1 | a0001c0001t0114g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGCCCCC others(5): Show |
1 | a0001c0001t0115g0215 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(12): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
A | ACGCCCCC others(6): Show |
1 | a0001c0001t0108g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+1468_15+1469ins others(13): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005394
|
AC | A | 18 | a0001c0001t0001g0211a0001c0001t0015g0007a0001c0001t0019g0208others(15): Show | 20 | HG00438.hp1 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.15+1482delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005394 | |||||
chrX:85005404
|
C | T | 11 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(8): Show | 11 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+1477C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005404 | ||||||
chrX:85005405
|
C | CCA | 4 | a0001c0001t0008g0085a0001c0001t0008g0086a0001c0001t0047g0011others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1479_15+1480ins others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005405 | |||||
chrX:85005474
|
T | TA | 252 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(249): Show | 255 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(252): Show |
intron_variant | MODIFIER | c.15+1549dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005474 | |||||
chrX:85005675
|
T | TGAATAAA others(19): Show |
4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1752_15+1777dup others(26): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005675 | |||||
chrX:85005735
|
AAC | A | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.15+1812_15+1813del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85005735 | |||||
chrX:85005819
|
C | T | 8 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0211others(5): Show | 8 | NA18960.hp1 NA18968.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+1892C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005819 | ||||||
chrX:85005899
|
C | A | 1 | a0001c0001t0004g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.15+1972C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85005899 | ||||||
chrX:85006053
|
C | T | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+2126C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006053 | ||||||
chrX:85006289
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+2362A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006289 | ||||||
chrX:85006334
|
GA | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+2408delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006334 | ||||||
chrX:85006343
|
A | G | 2 | a0001c0001t0003g0164a0001c0001t0013g0195 | 2 | NA19001.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.15+2416A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006343 | ||||||
chrX:85006557
|
T | TA | 5 | a0001c0001t0018g0168a0001c0001t0018g0197a0001c0001t0019g0208others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+2644dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85006557 | |||||
chrX:85006557
|
TA | T | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+2644delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85006557 | |||||
chrX:85006639
|
A | G | 3 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024 | 3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.15+2712A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006639 | ||||||
chrX:85006822
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(129): Show | 133 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.15+2895A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85006822 | ||||||
chrX:85007181
|
T | C | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+3254T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007181 | ||||||
chrX:85007222
|
G | T | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+3295G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007222 | ||||||
chrX:85007622
|
T | C | 2 | a0001c0001t0009g0124a0001c0001t0009g0169 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.15+3695T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007622 | ||||||
chrX:85007650
|
C | T | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+3723C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007650 | ||||||
chrX:85007802
|
C | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+3875C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007802 | ||||||
chrX:85007882
|
T | C | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+3955T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85007882 | ||||||
chrX:85008013
|
A | G | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.15+4086A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008013 | ||||||
chrX:85008060
|
T | TC | 1 | a0001c0001t0088g0050 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.15+4137dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008060 | |||||
chrX:85008315
|
C | G | 2 | a0001c0001t0022g0120a0001c0001t0022g0163 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.15+4388C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008315 | ||||||
chrX:85008411
|
A | G | 2 | a0001c0001t0109g0020a0001c0001t0110g0025 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.15+4484A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008411 | ||||||
chrX:85008534
|
G | GT | 9 | a0001c0001t0004g0224a0001c0001t0004g0227a0001c0001t0004g0228others(6): Show | 9 | HG01081.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+4609dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008534 | |||||
chrX:85008535
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0003g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.15+4608_15+4609ins others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008535 | ||||||
chrX:85008535
|
T | TTG | 5 | a0001c0001t0009g0128a0001c0001t0029g0212a0001c0001t0029g0213others(2): Show | 5 | HG00733.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+4646_15+4647dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTG | 8 | a0001c0001t0015g0007a0001c0001t0047g0011a0001c0001t0062g0016others(5): Show | 9 | HG00735.hp1 HG01346.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4644_15+4647dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTG | 11 | a0001c0001t0001g0102a0001c0001t0001g0172a0001c0001t0013g0195others(8): Show | 11 | HG00558.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+4642_15+4647dup others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTGT others(1): Show |
16 | a0001c0001t0001g0001a0001c0001t0001g0091a0001c0001t0001g0103others(13): Show | 17 | HG01175.hp2 HG01243.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.15+4640_15+4647dup others(8): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTGT others(3): Show |
36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0106others(33): Show | 36 | HG00642.hp1 HG01192.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.15+4638_15+4647dup others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTGT others(5): Show |
41 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0112others(38): Show | 41 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.15+4636_15+4647dup others(12): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTGT others(7): Show |
22 | a0001c0001t0001g0116a0001c0001t0001g0189a0001c0001t0001g0205others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.15+4634_15+4647dup others(14): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTGT others(9): Show |
5 | a0001c0001t0007g0157a0001c0001t0007g0193a0001c0001t0008g0101others(2): Show | 5 | HG02004.hp1 HG02602.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+4632_15+4647dup others(16): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTGT others(11): Show |
2 | a0001c0001t0021g0159a0001c0001t0059g0194 | 2 | NA18965.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.15+4630_15+4647dup others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTGT others(13): Show |
2 | a0001c0001t0007g0161a0001c0001t0021g0160 | 2 | NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.15+4628_15+4647dup others(20): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTGTGTGT others(15): Show |
3 | a0001c0001t0007g0162a0001c0001t0022g0120a0001c0001t0022g0163 | 3 | HG02257.hp1 HG03195.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.15+4626_15+4647dup others(22): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTTG | 1 | a0001c0001t0039g0220 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.15+4609_15+4610ins others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTTGTG | 3 | a0001c0001t0042g0222a0001c0001t0043g0221a0001c0001t0044g0218 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.15+4609_15+4610ins others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTTGTGTG | 10 | a0001c0001t0006g0238a0001c0001t0006g0242a0001c0001t0006g0244others(7): Show | 10 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+4609_15+4610ins others(7): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTTGTGTG others(2): Show |
1 | a0001c0001t0037g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.15+4609_15+4610ins others(9): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTTGTGTG others(4): Show |
1 | a0002c0002t0040g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.15+4609_15+4610ins others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
T | TTTGTGTG others(6): Show |
1 | a0001c0001t0006g0247 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.15+4609_15+4610ins others(13): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
TTG | T | 5 | a0001c0001t0032g0008a0001c0001t0033g0009a0001c0001t0036g0225others(2): Show | 5 | HG01168.hp2 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+4646_15+4647del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
TTGTG | T | 1 | a0001c0001t0023g0026 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.15+4644_15+4647del others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008535
|
TTGTGTG | T | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+4642_15+4647del others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85008535 | |||||
chrX:85008536
|
TGTG | T | 1 | a0001c0001t0004g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15+4610_15+4612del others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008536 | ||||||
chrX:85008575
|
A | G | 2 | a0001c0001t0012g0158a0001c0001t0012g0188 | 2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.15+4648A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008575 | ||||||
chrX:85008608
|
C | T | 6 | a0001c0001t0002g0098a0001c0001t0002g0153a0001c0001t0005g0088others(3): Show | 6 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+4681C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85008608 | ||||||
chrX:85009378
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.15+5451A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009378 | ||||||
chrX:85009592
|
A | G | 1 | a0001c0001t0003g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.15+5665A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009592 | ||||||
chrX:85009605
|
A | G | 3 | a0001c0001t0010g0006a0001c0001t0010g0192a0001c0001t0051g0006 | 3 | HG02922.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.15+5678A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009605 | ||||||
chrX:85009702
|
G | A | 1 | a0001c0001t0108g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+5775G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009702 | ||||||
chrX:85009816
|
G | A | 2 | a0001c0001t0009g0124a0001c0001t0009g0169 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.15+5889G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009816 | ||||||
chrX:85009892
|
A | G | 2 | a0001c0001t0080g0070a0001c0001t0082g0069 | 2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.15+5965A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009892 | ||||||
chrX:85009918
|
C | T | 2 | a0001c0001t0022g0120a0001c0001t0022g0163 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.15+5991C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009918 | ||||||
chrX:85009976
|
A | G | 1 | a0001c0001t0053g0152 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.15+6049A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85009976 | ||||||
chrX:85010218
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.15+6291T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010218 | ||||||
chrX:85010299
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+6372C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010299 | ||||||
chrX:85010309
|
T | C | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+6382T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010309 | ||||||
chrX:85010360
|
A | C | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+6433A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010360 | ||||||
chrX:85010436
|
T | C | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+6509T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010436 | ||||||
chrX:85010600
|
T | C | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6673T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85010600 | ||||||
chrX:85010969
|
TAA | T | 1 | a0001c0001t0039g0220 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.15+7045_15+7046del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85010969 | |||||
chrX:85011109
|
T | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18940.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.15+7182T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011109 | ||||||
chrX:85011168
|
A | G | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+7241A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011168 | ||||||
chrX:85011209
|
G | A | 1 | a0001c0001t0104g0027 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.15+7282G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011209 | ||||||
chrX:85011211
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.15+7284T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011211 | ||||||
chrX:85011428
|
A | T | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+7501A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011428 | ||||||
chrX:85011443
|
G | A | 1 | a0001c0001t0006g0247 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.15+7516G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011443 | ||||||
chrX:85011552
|
C | T | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+7625C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011552 | ||||||
chrX:85011553
|
A | G | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+7626A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011553 | ||||||
chrX:85011563
|
C | T | 2 | a0001c0001t0025g0046a0001c0001t0028g0068 | 2 | HG01074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.15+7636C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011563 | ||||||
chrX:85011693
|
G | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+7766G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85011693 | ||||||
chrX:85012000
|
G | C | 1 | a0001c0001t0072g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.15+8073G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012000 | ||||||
chrX:85012066
|
G | A | 3 | a0001c0001t0100g0028a0001c0001t0101g0029a0001c0001t0102g0055 | 3 | NA18985.hp1 NA19000.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.15+8139G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012066 | ||||||
chrX:85012498
|
A | G | 6 | a0001c0001t0047g0011a0001c0001t0106g0015a0001c0001t0109g0020others(3): Show | 6 | HG02647.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+8571A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012498 | ||||||
chrX:85012509
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+8582A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012509 | ||||||
chrX:85012804
|
C | CT | 1 | a0001c0001t0006g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15+8885dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85012804 | |||||
chrX:85012818
|
T | G | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+8891T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012818 | ||||||
chrX:85012964
|
A | G | 1 | a0001c0001t0004g0234 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+9037A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85012964 | ||||||
chrX:85013173
|
G | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0003g0180others(2): Show | 5 | HG00438.hp2 HG02056.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+9246G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013173 | ||||||
chrX:85013201
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+9274G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013201 | ||||||
chrX:85013563
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.15+9636A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013563 | ||||||
chrX:85013574
|
TG | T | 1 | a0001c0001t0088g0050 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.15+9649delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85013574 | |||||
chrX:85013692
|
T | A | 1 | a0001c0001t0008g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.15+9765T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013692 | ||||||
chrX:85013704
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.15+9777T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013704 | ||||||
chrX:85013951
|
T | C | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.15+10024T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013951 | ||||||
chrX:85013972
|
A | G | 1 | a0001c0001t0103g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15+10045A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85013972 | ||||||
chrX:85014165
|
C | T | 1 | a0001c0001t0087g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.15+10238C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014165 | ||||||
chrX:85014255
|
AT | A | 1 | a0001c0001t0088g0050 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.15+10333delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85014255 | |||||
chrX:85014333
|
T | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+10406T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014333 | ||||||
chrX:85014529
|
A | AT | 10 | a0001c0001t0001g0179a0001c0001t0023g0026a0001c0001t0028g0042others(7): Show | 10 | HG00673.hp1 HG02015.hp1 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+10615dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85014529 | |||||
chrX:85014529
|
AT | A | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+10615delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85014529 | |||||
chrX:85014543
|
G | A | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.15+10616G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014543 | ||||||
chrX:85014553
|
G | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+10626G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014553 | ||||||
chrX:85014566
|
CTTTA | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+10645_15+10648d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85014566 | |||||
chrX:85014802
|
A | G | 1 | a0001c0001t0008g0086 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+10875A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014802 | ||||||
chrX:85014842
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.15+10915C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014842 | ||||||
chrX:85014864
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+10937A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85014864 | ||||||
chrX:85015012
|
T | C | 5 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+11085T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015012 | ||||||
chrX:85015039
|
T | G | 1 | a0001c0001t0037g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.15+11112T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015039 | ||||||
chrX:85015228
|
T | A | 8 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0189others(5): Show | 8 | NA18961.hp1 NA18964.hp1 NA18993.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+11301T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015228 | ||||||
chrX:85015237
|
TA | T | 1 | a0001c0001t0019g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15+11317delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015237 | |||||
chrX:85015372
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+11445G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015372 | ||||||
chrX:85015377
|
T | C | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+11450T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015377 | ||||||
chrX:85015385
|
G | A | 1 | a0001c0001t0103g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15+11458G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015385 | ||||||
chrX:85015542
|
A | ATATT | 21 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0186others(18): Show | 22 | HG00733.hp2 HG01099.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.15+11655_15+11658d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015542 | |||||
chrX:85015542
|
A | ATATTTAT others(5): Show |
1 | a0001c0001t0056g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.15+11647_15+11658d others(14): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015542 | |||||
chrX:85015542
|
ATATT | A | 38 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0182others(35): Show | 38 | HG01081.hp2 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.15+11655_15+11658d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015542 | |||||
chrX:85015542
|
ATATTTAT others(1): Show |
A | 2 | a0001c0001t0001g0138a0001c0001t0014g0173 | 2 | HG01243.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.15+11651_15+11658d others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015542 | |||||
chrX:85015661
|
CG | C | 1 | a0001c0001t0088g0050 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.15+11737delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015661 | |||||
chrX:85015664
|
G | A | 1 | a0001c0001t0018g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.15+11737G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015664 | ||||||
chrX:85015742
|
AT | A | 1 | a0001c0001t0053g0152 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.15+11820delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85015742 | |||||
chrX:85015935
|
G | A | 1 | a0001c0001t0006g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15+12008G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85015935 | ||||||
chrX:85016012
|
G | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+12085G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016012 | ||||||
chrX:85016172
|
TG | T | 1 | a0001c0001t0053g0152 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.15+12247delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85016172 | |||||
chrX:85016204
|
T | C | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+12277T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016204 | ||||||
chrX:85016208
|
A | G | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+12281A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016208 | ||||||
chrX:85016263
|
C | T | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.15+12336C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016263 | ||||||
chrX:85016652
|
AG | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+12726delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016652 | ||||||
chrX:85016692
|
G | A | 1 | a0001c0001t0103g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15+12765G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016692 | ||||||
chrX:85016871
|
C | T | 2 | a0001c0001t0003g0164a0001c0001t0013g0195 | 2 | NA19001.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.15+12944C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016871 | ||||||
chrX:85016876
|
T | C | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+12949T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016876 | ||||||
chrX:85016971
|
G | T | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13044G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85016971 | ||||||
chrX:85017064
|
C | T | 1 | a0001c0001t0103g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15+13137C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017064 | ||||||
chrX:85017215
|
C | T | 4 | a0001c0001t0109g0020a0001c0001t0110g0025a0001c0001t0111g0052others(1): Show | 4 | HG02647.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+13288C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017215 | ||||||
chrX:85017257
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.15+13330T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017257 | ||||||
chrX:85017672
|
C | T | 9 | a0001c0001t0008g0085a0001c0001t0008g0086a0001c0001t0008g0101others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+13745C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017672 | ||||||
chrX:85017684
|
G | A | 3 | a0001c0001t0027g0058a0001c0001t0088g0050a0001c0001t0089g0057 | 3 | NA18971.hp1 NA19001.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.15+13757G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017684 | ||||||
chrX:85017810
|
T | C | 1 | a0001c0001t0108g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.15+13883T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017810 | ||||||
chrX:85017886
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+13959A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017886 | ||||||
chrX:85017898
|
C | T | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13971C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85017898 | ||||||
chrX:85018246
|
G | A | 2 | a0001c0001t0080g0070a0001c0001t0082g0069 | 2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.15+14319G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85018246 | ||||||
chrX:85018324
|
T | C | 1 | a0001c0001t0112g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.15+14397T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85018324 | ||||||
chrX:85018353
|
G | A | 1 | a0001c0001t0121g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.15+14426G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85018353 | ||||||
chrX:85018578
|
C | CT | 8 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+14662dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85018578 | |||||
chrX:85018746
|
TTC | T | 1 | a0001c0001t0090g0010 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.15+14821_15+14822d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85018746 | |||||
chrX:85018942
|
GT | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.15+15019delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85018942 | |||||
chrX:85019025
|
C | T | 1 | a0001c0001t0012g0204 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.15+15098C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019025 | ||||||
chrX:85019112
|
G | A | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+15185G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019112 | ||||||
chrX:85019216
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 114 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.15+15289A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019216 | ||||||
chrX:85019219
|
T | C | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+15292T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019219 | ||||||
chrX:85019265
|
AT | A | 3 | a0001c0001t0001g0116a0001c0001t0002g0115a0001c0001t0002g0117 | 3 | HG00140.hp1 HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.15+15339delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019265 | ||||||
chrX:85019654
|
C | T | 12 | a0001c0001t0006g0238a0001c0001t0006g0242a0001c0001t0006g0244others(9): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+15727C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019654 | ||||||
chrX:85019694
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.15+15767A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019694 | ||||||
chrX:85019907
|
A | G | 3 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024 | 3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.15+15980A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019907 | ||||||
chrX:85019997
|
C | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+16070C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85019997 | ||||||
chrX:85020243
|
A | G | 1 | a0001c0001t0049g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.15+16316A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85020243 | ||||||
chrX:85020292
|
G | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+16365G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85020292 | ||||||
chrX:85020676
|
T | C | 29 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(26): Show | 29 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.15+16749T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85020676 | ||||||
chrX:85020921
|
C | T | 11 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(8): Show | 11 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+16994C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85020921 | ||||||
chrX:85021014
|
A | G | 2 | a0001c0001t0052g0148a0001c0001t0056g0150 | 2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.15+17087A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021014 | ||||||
chrX:85021065
|
A | T | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+17138A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021065 | ||||||
chrX:85021107
|
G | C | 1 | a0001c0001t0111g0052 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.15+17180G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021107 | ||||||
chrX:85021276
|
C | T | 1 | a0001c0001t0116g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+17349C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021276 | ||||||
chrX:85021477
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(185): Show | 190 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.15+17550G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021477 | ||||||
chrX:85021644
|
GCT | G | 5 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+17719_15+17720d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85021644 | |||||
chrX:85021850
|
CCTT | C | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+17924_15+17926d others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85021850 | ||||||
chrX:85022229
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(176): Show | 180 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.15+18302T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85022229 | ||||||
chrX:85022259
|
A | C | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+18332A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85022259 | ||||||
chrX:85022281
|
A | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.15+18354A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85022281 | ||||||
chrX:85022641
|
AAAAGCT | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+18724_15+18729d others(8): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85022641 | |||||
chrX:85022659
|
C | T | 1 | a0001c0001t0003g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15+18732C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85022659 | ||||||
chrX:85023224
|
G | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG01257.hp2 HG02698.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+19297G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85023224 | ||||||
chrX:85023327
|
A | G | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+19400A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85023327 | ||||||
chrX:85023619
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+19692A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85023619 | ||||||
chrX:85023682
|
C | T | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.15+19755C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85023682 | ||||||
chrX:85024086
|
G | T | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+20159G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024086 | ||||||
chrX:85024229
|
T | C | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+20302T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024229 | ||||||
chrX:85024275
|
T | C | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.15+20348T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024275 | ||||||
chrX:85024313
|
T | C | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+20386T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024313 | ||||||
chrX:85024350
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.15+20423A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024350 | ||||||
chrX:85024449
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.15+20522T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024449 | ||||||
chrX:85024482
|
C | T | 3 | a0001c0001t0001g0211a0001c0001t0003g0165a0001c0001t0003g0196 | 3 | NA18960.hp1 NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.15+20555C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024482 | ||||||
chrX:85024841
|
C | T | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+20914C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024841 | ||||||
chrX:85024951
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.15+21024A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85024951 | ||||||
chrX:85025035
|
C | T | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.15+21108C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025035 | ||||||
chrX:85025094
|
G | A | 32 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(29): Show | 32 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.15+21167G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025094 | ||||||
chrX:85025135
|
TC | T | 1 | a0001c0001t0001g0096 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.15+21211delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85025135 | |||||
chrX:85025304
|
C | T | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-21142C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025304 | ||||||
chrX:85025577
|
C | T | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-20869C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025577 | ||||||
chrX:85025612
|
T | C | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-20834T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025612 | ||||||
chrX:85025634
|
A | G | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-20812A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025634 | ||||||
chrX:85025665
|
C | CA | 2 | a0001c0001t0076g0031a0001c0001t0091g0059 | 2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.16-20780dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85025665 | |||||
chrX:85025987
|
C | T | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-20459C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85025987 | ||||||
chrX:85026509
|
G | T | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-19937G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026509 | ||||||
chrX:85026511
|
T | G | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-19935T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026511 | ||||||
chrX:85026658
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.16-19788C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026658 | ||||||
chrX:85026668
|
G | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(167): Show | 171 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.16-19778G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026668 | ||||||
chrX:85026733
|
AG | A | 3 | a0001c0001t0042g0222a0001c0001t0043g0221a0001c0001t0044g0218 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.16-19711delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85026733 | |||||
chrX:85026772
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.16-19674C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026772 | ||||||
chrX:85026910
|
C | T | 2 | a0001c0001t0022g0120a0001c0001t0022g0163 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-19536C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85026910 | ||||||
chrX:85027068
|
G | A | 1 | a0001c0001t0004g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.16-19378G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027068 | ||||||
chrX:85027262
|
G | A | 7 | a0001c0001t0009g0124a0001c0001t0009g0128a0001c0001t0009g0169others(4): Show | 7 | HG02257.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-19184G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027262 | ||||||
chrX:85027324
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.16-19122T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027324 | ||||||
chrX:85027335
|
G | GC | 1 | a0001c0001t0101g0029 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.16-19106dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85027335 | |||||
chrX:85027722
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.16-18724T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027722 | ||||||
chrX:85027884
|
A | T | 1 | a0001c0001t0063g0051 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-18562A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85027884 | ||||||
chrX:85028238
|
C | T | 8 | a0001c0001t0028g0042a0001c0001t0045g0044a0001c0001t0060g0022others(5): Show | 8 | HG02015.hp1 NA18967.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-18208C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85028238 | ||||||
chrX:85028406
|
G | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-18040G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85028406 | ||||||
chrX:85028634
|
A | AT | 6 | a0001c0001t0004g0226a0001c0001t0032g0008a0001c0001t0033g0009others(3): Show | 6 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-17798dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85028634 | |||||
chrX:85028695
|
C | G | 4 | a0001c0001t0024g0004a0001c0001t0067g0083a0001c0001t0068g0082others(1): Show | 5 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-17751C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85028695 | ||||||
chrX:85028740
|
ATTCAATG others(2): Show |
A | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.16-17703_16-17695d others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85028740 | |||||
chrX:85028909
|
AC | A | 2 | a0001c0001t0001g0106a0001c0001t0054g0141 | 2 | HG00642.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.16-17533delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85028909 | |||||
chrX:85029164
|
G | A | 1 | a0001c0001t0004g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.16-17282G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029164 | ||||||
chrX:85029241
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.16-17205A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029241 | ||||||
chrX:85029558
|
A | G | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-16888A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029558 | ||||||
chrX:85029854
|
A | G | 8 | a0001c0001t0001g0104a0001c0001t0001g0147a0001c0001t0001g0176others(5): Show | 8 | HG01934.hp1 NA18944.hp1 NA18986.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-16592A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029854 | ||||||
chrX:85029945
|
A | T | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-16501A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029945 | ||||||
chrX:85029970
|
G | C | 1 | a0001c0001t0025g0046 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.16-16476G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85029970 | ||||||
chrX:85030155
|
GC | G | 5 | a0001c0001t0018g0168a0001c0001t0018g0197a0001c0001t0019g0208others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-16290delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85030155 | ||||||
chrX:85030175
|
A | G | 2 | a0001c0001t0009g0128a0001c0001t0011g0127 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.16-16271A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85030175 | ||||||
chrX:85030319
|
C | T | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-16127C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85030319 | ||||||
chrX:85030809
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-15637G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85030809 | ||||||
chrX:85031163
|
A | G | 1 | a0001c0001t0014g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.16-15283A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85031163 | ||||||
chrX:85031456
|
A | T | 3 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0116g0073 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.16-14990A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85031456 | ||||||
chrX:85031896
|
C | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-14550C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85031896 | ||||||
chrX:85032122
|
T | G | 9 | a0001c0001t0009g0124a0001c0001t0009g0128a0001c0001t0009g0169others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-14324T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032122 | ||||||
chrX:85032243
|
G | A | 4 | a0001c0001t0032g0008a0001c0001t0033g0009a0001c0001t0047g0011others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-14203G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032243 | ||||||
chrX:85032331
|
A | G | 4 | a0001c0001t0002g0098a0001c0001t0002g0153a0001c0001t0005g0088others(1): Show | 4 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-14115A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032331 | ||||||
chrX:85032445
|
C | T | 1 | a0001c0001t0008g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.16-14001C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032445 | ||||||
chrX:85032469
|
G | A | 1 | a0001c0001t0010g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-13977G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032469 | ||||||
chrX:85032470
|
C | G | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-13976C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032470 | ||||||
chrX:85032470
|
C | T | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-13976C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032470 | ||||||
chrX:85032471
|
G | A | 7 | a0001c0001t0024g0004a0001c0001t0067g0083a0001c0001t0068g0082others(4): Show | 8 | HG00438.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-13975G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032471 | ||||||
chrX:85032514
|
C | CA | 5 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-13917dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85032514 | |||||
chrX:85032514
|
CA | C | 1 | a0001c0001t0074g0065 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.16-13917delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85032514 | |||||
chrX:85032589
|
T | C | 1 | a0001c0001t0023g0026 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.16-13857T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032589 | ||||||
chrX:85032599
|
A | G | 12 | a0001c0001t0006g0238a0001c0001t0006g0242a0001c0001t0006g0244others(9): Show | 12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.16-13847A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032599 | ||||||
chrX:85032917
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-13529A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032917 | ||||||
chrX:85032967
|
A | T | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-13479A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85032967 | ||||||
chrX:85033148
|
A | G | 1 | a0001c0001t0109g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.16-13298A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033148 | ||||||
chrX:85033353
|
G | A | 3 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0116g0073 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.16-13093G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033353 | ||||||
chrX:85033384
|
G | A | 1 | a0001c0001t0006g0246 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.16-13062G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033384 | ||||||
chrX:85033500
|
A | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-12946A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033500 | ||||||
chrX:85033669
|
T | A | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-12777T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033669 | ||||||
chrX:85033720
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.16-12726T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033720 | ||||||
chrX:85033848
|
G | T | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-12598G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85033848 | ||||||
chrX:85034177
|
TA | T | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.16-12259delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85034177 | |||||
chrX:85034421
|
A | G | 3 | a0001c0001t0009g0170a0001c0001t0011g0126a0001c0001t0011g0198 | 3 | HG02257.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.16-12025A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034421 | ||||||
chrX:85034424
|
G | A | 1 | a0001c0001t0104g0027 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.16-12022G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034424 | ||||||
chrX:85034458
|
G | GT | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-11978dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85034458 | |||||
chrX:85034608
|
T | C | 1 | a0001c0001t0063g0051 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-11838T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034608 | ||||||
chrX:85034637
|
C | T | 1 | a0001c0001t0049g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16-11809C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034637 | ||||||
chrX:85034719
|
T | A | 1 | a0001c0001t0056g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.16-11727T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034719 | ||||||
chrX:85034720
|
T | A | 1 | a0001c0001t0056g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.16-11726T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85034720 | ||||||
chrX:85035058
|
C | G | 15 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(12): Show | 15 | HG01081.hp2 HG01109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.16-11388C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85035058 | ||||||
chrX:85035285
|
T | TC | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.16-11157dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85035285 | |||||
chrX:85035558
|
T | A | 37 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(34): Show | 37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-10888T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85035558 | ||||||
chrX:85036254
|
G | T | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-10192G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036254 | ||||||
chrX:85036271
|
C | T | 2 | a0001c0001t0109g0020a0001c0001t0110g0025 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.16-10175C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036271 | ||||||
chrX:85036277
|
C | G | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-10169C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036277 | ||||||
chrX:85036545
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-9901A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036545 | ||||||
chrX:85036723
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-9723T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036723 | ||||||
chrX:85036820
|
C | CG | 1 | a0001c0001t0001g0147 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.16-9626_16-9625ins others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036820 | ||||||
chrX:85036821
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.16-9625A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036821 | ||||||
chrX:85036872
|
C | CA | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.16-9574_16-9573ins others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85036872 | ||||||
chrX:85037208
|
A | AG | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.16-9238_16-9237ins others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85037208 | ||||||
chrX:85037313
|
C | T | 7 | a0001c0001t0009g0124a0001c0001t0009g0128a0001c0001t0009g0169others(4): Show | 7 | HG02257.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-9133C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85037313 | ||||||
chrX:85037432
|
G | A | 1 | a0001c0001t0112g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.16-9014G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85037432 | ||||||
chrX:85037465
|
TC | T | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.16-8978delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85037465 | |||||
chrX:85037772
|
C | T | 1 | a0001c0001t0004g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.16-8674C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85037772 | ||||||
chrX:85038011
|
C | CA | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.16-8431dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038011 | |||||
chrX:85038224
|
C | T | 2 | a0001c0001t0003g0165a0001c0001t0003g0196 | 2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.16-8222C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85038224 | ||||||
chrX:85038254
|
G | T | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-8192G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85038254 | ||||||
chrX:85038524
|
G | GT | 15 | a0001c0001t0023g0064a0001c0001t0029g0212a0001c0001t0029g0213others(12): Show | 15 | HG01168.hp2 HG01346.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.16-7896dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTT | 5 | a0001c0001t0063g0051a0001c0001t0065g0018a0001c0001t0066g0047others(2): Show | 5 | HG00735.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-7897_16-7896dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTT | 4 | a0001c0001t0006g0238a0001c0001t0006g0242a0001c0001t0006g0247others(1): Show | 4 | HG01169.hp1 HG02451.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-7898_16-7896dup others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTTT | 5 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0016g0239others(2): Show | 5 | HG01167.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-7899_16-7896dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTTTT | 3 | a0001c0001t0017g0240a0001c0001t0034g0236a0001c0001t0041g0241 | 3 | HG00738.hp1 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.16-7900_16-7896dup others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0111g0052 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.16-7909_16-7896dup others(14): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0106g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.16-7913_16-7896dup others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTTTTTT others(13): Show |
1 | a0001c0001t0112g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.16-7915_16-7896dup others(20): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTTTTTT others(14): Show |
1 | a0001c0001t0109g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.16-7916_16-7896dup others(21): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0110g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.16-7920_16-7896dup others(25): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
G | GTTTTTTT others(28): Show |
1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-7896_16-7895ins others(35): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
GT | G | 6 | a0001c0001t0015g0007a0001c0001t0023g0026a0001c0001t0026g0078others(3): Show | 7 | HG00673.hp1 HG01106.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-7896delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
GTT | G | 1 | a0001c0001t0004g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.16-7897_16-7896del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
GTTT | G | 22 | a0001c0001t0001g0138a0001c0001t0001g0206a0001c0001t0002g0095others(19): Show | 22 | HG01081.hp2 HG01175.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.16-7898_16-7896del others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
GTTTT | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(124): Show | 128 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.16-7899_16-7896del others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
GTTTTT | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0211a0001c0001t0049g0171 | 3 | NA18960.hp1 NA18986.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.16-7900_16-7896del others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
GTTTTTTT | G | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-7902_16-7896del others(7): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-7906_16-7896del others(11): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038524
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0024g0004 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.16-7909_16-7896del others(14): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038524 | |||||
chrX:85038530
|
T | G | 1 | a0001c0001t0082g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.16-7916T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85038530 | ||||||
chrX:85038914
|
G | C | 2 | a0001c0001t0076g0031a0001c0001t0091g0059 | 2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.16-7532G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85038914 | ||||||
chrX:85038964
|
GT | G | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.16-7477delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85038964 | |||||
chrX:85039052
|
T | C | 1 | a0001c0001t0122g0063 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.16-7394T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039052 | ||||||
chrX:85039207
|
A | G | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-7239A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039207 | ||||||
chrX:85039230
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(185): Show | 190 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.16-7216C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039230 | ||||||
chrX:85039233
|
C | CT | 1 | a0001c0001t0039g0220 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.16-7201dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85039233 | |||||
chrX:85039233
|
CT | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-7201delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85039233 | |||||
chrX:85039254
|
G | A | 1 | a0001c0001t0084g0017 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.16-7192G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039254 | ||||||
chrX:85039297
|
T | C | 37 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(34): Show | 37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-7149T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039297 | ||||||
chrX:85039500
|
T | TG | 1 | a0001c0001t0088g0050 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.16-6942dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85039500 | |||||
chrX:85039520
|
C | G | 1 | a0001c0001t0083g0039 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.16-6926C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039520 | ||||||
chrX:85039580
|
T | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-6866T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039580 | ||||||
chrX:85039828
|
C | T | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-6618C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039828 | ||||||
chrX:85039896
|
A | C | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-6550A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039896 | ||||||
chrX:85039952
|
G | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-6494G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039952 | ||||||
chrX:85039961
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-6485T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85039961 | ||||||
chrX:85040175
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.16-6271A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040175 | ||||||
chrX:85040210
|
A | G | 9 | a0001c0001t0008g0085a0001c0001t0008g0086a0001c0001t0008g0101others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-6236A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040210 | ||||||
chrX:85040224
|
C | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-6222C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040224 | ||||||
chrX:85040459
|
G | A | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.16-5987G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040459 | ||||||
chrX:85040708
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-5738T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040708 | ||||||
chrX:85040718
|
A | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-5728A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040718 | ||||||
chrX:85040739
|
G | A | 5 | a0001c0001t0018g0168a0001c0001t0018g0197a0001c0001t0019g0208others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-5707G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040739 | ||||||
chrX:85040976
|
G | A | 3 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024 | 3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.16-5470G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85040976 | ||||||
chrX:85041111
|
G | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-5335G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85041111 | ||||||
chrX:85041121
|
AG | A | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.16-5322delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85041121 | |||||
chrX:85041263
|
TA | T | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.16-5181delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85041263 | |||||
chrX:85041421
|
A | T | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-5025A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85041421 | ||||||
chrX:85041639
|
TG | T | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.16-4804delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85041639 | |||||
chrX:85041694
|
A | G | 1 | a0001c0001t0007g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.16-4752A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85041694 | ||||||
chrX:85041727
|
G | A | 1 | a0001c0001t0005g0119 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.16-4719G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85041727 | ||||||
chrX:85041827
|
G | GC | 1 | a0001c0001t0088g0050 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.16-4612dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85041827 | |||||
chrX:85042034
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-4412T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85042034 | ||||||
chrX:85042473
|
GA | G | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.16-3969delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85042473 | |||||
chrX:85042528
|
G | A | 8 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0062g0016others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-3918G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85042528 | ||||||
chrX:85042673
|
CA | C | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.16-3768delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85042673 | |||||
chrX:85042690
|
A | G | 2 | a0001c0001t0009g0124a0001c0001t0009g0169 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.16-3756A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85042690 | ||||||
chrX:85042934
|
G | A | 1 | a0001c0001t0034g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.16-3512G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85042934 | ||||||
chrX:85043090
|
G | A | 1 | a0001c0001t0077g0021 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.16-3356G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043090 | ||||||
chrX:85043174
|
A | T | 37 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(34): Show | 37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-3272A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043174 | ||||||
chrX:85043232
|
C | T | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-3214C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043232 | ||||||
chrX:85043258
|
G | T | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-3188G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043258 | ||||||
chrX:85043269
|
C | T | 37 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(34): Show | 37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.16-3177C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043269 | ||||||
chrX:85043331
|
G | C | 1 | a0001c0001t0004g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.16-3115G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043331 | ||||||
chrX:85043410
|
A | AT | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.16-3022dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85043410 | |||||
chrX:85043410
|
A | ATT | 2 | a0001c0001t0002g0095a0001c0001t0002g0145 | 2 | NA18975.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.16-3023_16-3022dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85043410 | |||||
chrX:85043410
|
AT | A | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-3022delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85043410 | |||||
chrX:85043467
|
A | C | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-2979A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043467 | ||||||
chrX:85043584
|
CT | C | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.16-2856delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85043584 | |||||
chrX:85043679
|
C | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0117 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.16-2767C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043679 | ||||||
chrX:85043683
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.16-2763G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043683 | ||||||
chrX:85043771
|
A | C | 1 | a0001c0001t0002g0145 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.16-2675A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043771 | ||||||
chrX:85043775
|
C | T | 2 | a0001c0001t0022g0120a0001c0001t0022g0163 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.16-2671C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043775 | ||||||
chrX:85043800
|
A | G | 3 | a0001c0001t0042g0222a0001c0001t0043g0221a0001c0001t0044g0218 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.16-2646A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043800 | ||||||
chrX:85043818
|
GA | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-2623delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85043818 | |||||
chrX:85043906
|
G | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.16-2540G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043906 | ||||||
chrX:85043964
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-2482A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85043964 | ||||||
chrX:85044000
|
T | TC | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.16-2446_16-2445ins others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044000 | ||||||
chrX:85044052
|
T | TA | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-2393dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044052 | |||||
chrX:85044090
|
TG | T | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-2354delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044090 | |||||
chrX:85044182
|
A | G | 8 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0189others(5): Show | 8 | NA18961.hp1 NA18964.hp1 NA18993.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-2264A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044182 | ||||||
chrX:85044252
|
T | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-2194T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044252 | ||||||
chrX:85044254
|
A | ATG | 102 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(99): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.16-2176_16-2175dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044254 | |||||
chrX:85044254
|
A | ATGTG | 4 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG01257.hp2 HG02698.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2178_16-2175dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044254 | |||||
chrX:85044270
|
G | GTA | 1 | a0001c0001t0106g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.16-2162_16-2161dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044270 | |||||
chrX:85044270
|
G | GTGTA | 32 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0123others(29): Show | 32 | HG00609.hp1 HG01934.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.16-2175_16-2174ins others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044270 | |||||
chrX:85044272
|
A | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.16-2174A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044272 | ||||||
chrX:85044288
|
A | AT | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-2151dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044288 | |||||
chrX:85044356
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(181): Show | 185 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.16-2090G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044356 | ||||||
chrX:85044374
|
TG | T | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-2069delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85044374 | |||||
chrX:85044515
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.16-1931A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044515 | ||||||
chrX:85044519
|
G | GT | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-1927_16-1926ins others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044519 | ||||||
chrX:85044605
|
G | C | 1 | a0001c0001t0065g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.16-1841G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044605 | ||||||
chrX:85044635
|
G | A | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.16-1811G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044635 | ||||||
chrX:85044851
|
T | A | 1 | a0001c0001t0090g0010 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.16-1595T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85044851 | ||||||
chrX:85045184
|
AG | A | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-1259delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045184 | |||||
chrX:85045230
|
C | T | 3 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0116g0073 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.16-1216C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85045230 | ||||||
chrX:85045256
|
TA | T | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-1181delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045256 | |||||
chrX:85045291
|
A | AT | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-1151dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045291 | |||||
chrX:85045335
|
GC | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-1108delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045335 | |||||
chrX:85045407
|
TA | T | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-1034delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045407 | |||||
chrX:85045467
|
T | TC | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-977dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045467 | |||||
chrX:85045592
|
T | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.16-854T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85045592 | ||||||
chrX:85045663
|
T | TG | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-781dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045663 | |||||
chrX:85045733
|
A | AG | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-712dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045733 | |||||
chrX:85045793
|
GA | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-651delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85045793 | |||||
chrX:85045836
|
G | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0002g0175 | 3 | NA18961.hp1 NA19082.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.16-610G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85045836 | ||||||
chrX:85045932
|
C | T | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16-514C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85045932 | ||||||
chrX:85046008
|
A | G | 9 | a0001c0001t0009g0124a0001c0001t0009g0128a0001c0001t0009g0169others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-438A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85046008 | ||||||
chrX:85046073
|
TG | T | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-371delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85046073 | |||||
chrX:85046077
|
A | G | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-369A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | chrX | 85046077 | ||||||
chrX:85046373
|
TC | T | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.16-71delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chrX | 85046373 | |||||
chrX:85046584
|
T | TA | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+36dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85046584 | |||||
chrX:85046616
|
TA | T | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+70delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85046616 | |||||
chrX:85046629
|
GC | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+82delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85046629 | |||||
chrX:85046793
|
G | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.120+243G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85046793 | ||||||
chrX:85046877
|
T | TA | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+329dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85046877 | |||||
chrX:85046933
|
A | AC | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+385dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85046933 | |||||
chrX:85046962
|
A | G | 1 | a0001c0001t0003g0107 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.120+412A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85046962 | ||||||
chrX:85046965
|
G | C | 2 | a0001c0001t0100g0028a0001c0001t0101g0029 | 2 | NA18985.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.120+415G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85046965 | ||||||
chrX:85047109
|
T | TG | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+559_120+560ins others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047109 | ||||||
chrX:85047163
|
CA | C | 2 | a0001c0001t0001g0182a0001c0001t0079g0235 | 2 | NA18959.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.120+619delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85047163 | |||||
chrX:85047281
|
C | T | 3 | a0001c0001t0042g0222a0001c0001t0043g0221a0001c0001t0044g0218 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.120+731C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047281 | ||||||
chrX:85047328
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.120+778C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047328 | ||||||
chrX:85047331
|
G | A | 1 | a0001c0001t0110g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.120+781G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047331 | ||||||
chrX:85047377
|
T | G | 1 | a0001c0001t0012g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.120+827T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047377 | ||||||
chrX:85047510
|
C | A | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.120+960C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85047510 | ||||||
chrX:85047586
|
C | CT | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+1041dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85047586 | |||||
chrX:85047674
|
A | AT | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.120+1125dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85047674 | |||||
chrX:85048292
|
A | AT | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.120+1748dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85048292 | |||||
chrX:85048519
|
T | A | 3 | a0001c0001t0042g0222a0001c0001t0043g0221a0001c0001t0044g0218 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.120+1969T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85048519 | ||||||
chrX:85048602
|
AG | A | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.120+2055delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85048602 | |||||
chrX:85048651
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.120+2101G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85048651 | ||||||
chrX:85048896
|
C | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(179): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.120+2346C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85048896 | ||||||
chrX:85049055
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.121-2334A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049055 | ||||||
chrX:85049074
|
G | A | 1 | a0001c0001t0054g0141 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.121-2315G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049074 | ||||||
chrX:85049464
|
G | A | 4 | a0001c0001t0003g0092a0001c0001t0010g0006a0001c0001t0010g0192others(1): Show | 4 | HG02922.hp1 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-1925G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049464 | ||||||
chrX:85049594
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.121-1795G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049594 | ||||||
chrX:85049787
|
AAAAC | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.121-1586_121-1583d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85049787 | |||||
chrX:85049987
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.121-1402C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85049987 | ||||||
chrX:85050129
|
TA | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(176): Show | 181 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.121-1256delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85050129 | |||||
chrX:85050142
|
C | T | 3 | a0001c0001t0008g0202a0001c0001t0014g0173a0001c0001t0014g0201 | 3 | HG01243.hp1 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.121-1247C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050142 | ||||||
chrX:85050263
|
AG | A | 1 | a0001c0001t0001g0248 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.121-1125delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050263 | ||||||
chrX:85050264
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(175): Show | 180 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.121-1125G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050264 | ||||||
chrX:85050266
|
T | A | 1 | a0001c0001t0001g0248 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.121-1123T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050266 | ||||||
chrX:85050287
|
G | T | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.121-1102G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050287 | ||||||
chrX:85050606
|
C | CA | 8 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0206others(5): Show | 9 | HG02055.hp1 HG02602.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-767dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85050606 | |||||
chrX:85050606
|
CA | C | 32 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(29): Show | 32 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.121-767delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85050606 | |||||
chrX:85050622
|
AT | A | 1 | a0001c0001t0001g0178 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.121-758delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85050622 | |||||
chrX:85050721
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18940.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.121-668G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050721 | ||||||
chrX:85050963
|
A | G | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.121-426A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85050963 | ||||||
chrX:85051054
|
G | A | 1 | a0001c0001t0046g0040 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.121-335G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85051054 | ||||||
chrX:85051209
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.121-180G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | chrX | 85051209 | ||||||
chrX:85051374
|
A | AT | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.121-9dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chrX | 85051374 | |||||
chrX:85051641
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.240+133T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85051641 | ||||||
chrX:85051779
|
GCA | G | 1 | a0001c0001t0081g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.240+273_240+274del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 85051779 | |||||
chrX:85051809
|
G | A | 1 | a0001c0001t0057g0114 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.240+301G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85051809 | ||||||
chrX:85052000
|
A | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.240+492A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052000 | ||||||
chrX:85052251
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.240+743C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052251 | ||||||
chrX:85052800
|
A | G | 29 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(26): Show | 29 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.240+1292A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052800 | ||||||
chrX:85052911
|
CA | C | 2 | a0001c0001t0001g0134a0001c0001t0003g0093 | 2 | NA18950.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.240+1404delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052911 | ||||||
chrX:85052943
|
TC | T | 1 | a0001c0001t0004g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241-1399delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 85052943 | |||||
chrX:85052945
|
C | A | 1 | a0001c0001t0004g0229 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241-1399C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85052945 | ||||||
chrX:85053105
|
G | A | 5 | a0001c0001t0018g0168a0001c0001t0018g0197a0001c0001t0019g0208others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-1239G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053105 | ||||||
chrX:85053208
|
A | T | 1 | a0001c0001t0087g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.241-1136A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053208 | ||||||
chrX:85053346
|
G | A | 1 | a0001c0001t0037g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.241-998G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053346 | ||||||
chrX:85053452
|
A | T | 1 | a0001c0001t0067g0083 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.241-892A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053452 | ||||||
chrX:85053950
|
C | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.241-394C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85053950 | ||||||
chrX:85054074
|
A | AT | 1 | a0001c0001t0001g0206 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.241-263dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 85054074 | |||||
chrX:85054211
|
G | A | 1 | a0001c0001t0054g0141 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.241-133G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85054211 | ||||||
chrX:85054249
|
A | G | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.241-95A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | chrX | 85054249 | ||||||
chrX:85054339
|
C | CT | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.241-3dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chrX | 85054339 | |||||
chrX:85054426
|
T | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.295+28T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85054426 | ||||||
chrX:85054543
|
TATTG | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.295+149_295+152del others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 85054543 | |||||
chrX:85054620
|
T | TTG | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.295+224_295+225dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chrX | 85054620 | |||||
chrX:85054951
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.295+553G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85054951 | ||||||
chrX:85055011
|
C | T | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.295+613C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85055011 | ||||||
chrX:85055319
|
G | A | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-508G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85055319 | ||||||
chrX:85055623
|
G | A | 1 | a0001c0001t0017g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.296-204G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 4/8 | chrX | 85055623 | ||||||
chrX:85055932
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
splice_region_variant&intron_variant | LOW | c.394+7T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85055932 | ||||||
chrX:85056175
|
A | G | 1 | a0001c0001t0037g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.394+250A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056175 | ||||||
chrX:85056235
|
A | G | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+310A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056235 | ||||||
chrX:85056355
|
T | G | 29 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(26): Show | 29 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.394+430T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056355 | ||||||
chrX:85056534
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA18940.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.394+609G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056534 | ||||||
chrX:85056789
|
T | C | 16 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+864T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056789 | ||||||
chrX:85056821
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.394+896T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056821 | ||||||
chrX:85056926
|
A | G | 2 | a0001c0001t0022g0120a0001c0001t0022g0163 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.394+1001A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85056926 | ||||||
chrX:85057094
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.394+1169G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057094 | ||||||
chrX:85057148
|
AT | A | 16 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+1225delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85057148 | |||||
chrX:85057183
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+1258G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057183 | ||||||
chrX:85057387
|
C | T | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+1462C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057387 | ||||||
chrX:85057463
|
C | CAT | 1 | a0001c0001t0121g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.394+1550_394+1551d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85057463 | |||||
chrX:85057496
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.394+1571A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057496 | ||||||
chrX:85057638
|
GATATATA others(19): Show |
G | 1 | a0001c0001t0094g0032 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.394+1748_394+1773d others(28): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85057638 | |||||
chrX:85057666
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.394+1741T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057666 | ||||||
chrX:85057701
|
A | C | 1 | a0001c0001t0080g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.394+1776A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057701 | ||||||
chrX:85057949
|
G | A | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+2024G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85057949 | ||||||
chrX:85058062
|
CT | C | 1 | a0001c0001t0093g0077 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.394+2144delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85058062 | |||||
chrX:85058063
|
T | C | 1 | a0001c0001t0053g0152 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.394+2138T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058063 | ||||||
chrX:85058075
|
A | G | 1 | a0001c0001t0087g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.394+2150A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058075 | ||||||
chrX:85058094
|
G | T | 2 | a0001c0001t0080g0070a0001c0001t0082g0069 | 2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.394+2169G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058094 | ||||||
chrX:85058096
|
T | A | 1 | a0001c0001t0034g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394+2171T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058096 | ||||||
chrX:85058287
|
T | C | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.394+2362T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058287 | ||||||
chrX:85058409
|
C | A | 1 | a0001c0001t0078g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.394+2484C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058409 | ||||||
chrX:85058692
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.394+2767C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058692 | ||||||
chrX:85058795
|
G | C | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+2870G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058795 | ||||||
chrX:85058834
|
C | CT | 1 | a0001c0001t0109g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.394+2916dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85058834 | |||||
chrX:85058881
|
TTTA | T | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+2967_394+2969d others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85058881 | |||||
chrX:85058944
|
G | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.394+3019G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85058944 | ||||||
chrX:85059021
|
T | TC | 3 | a0001c0001t0001g0147a0001c0001t0093g0077a0001c0001t0114g0216 | 3 | HG02145.hp1 NA19058.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.394+3102dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85059021 | |||||
chrX:85059028
|
G | GC | 1 | a0001c0001t0100g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394+3109dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85059028 | |||||
chrX:85059051
|
C | T | 3 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0116g0073 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394+3126C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059051 | ||||||
chrX:85059098
|
A | G | 1 | a0001c0001t0049g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394+3173A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059098 | ||||||
chrX:85059217
|
T | G | 5 | a0001c0001t0018g0168a0001c0001t0018g0197a0001c0001t0019g0208others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+3292T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059217 | ||||||
chrX:85059285
|
C | T | 1 | a0001c0001t0103g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.394+3360C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059285 | ||||||
chrX:85059339
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.394+3414C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059339 | ||||||
chrX:85059415
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.394+3490A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059415 | ||||||
chrX:85059468
|
C | G | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.394+3543C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059468 | ||||||
chrX:85059468
|
CGTT | C | 1 | a0001c0001t0102g0055 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.394+3545_394+3547d others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85059468 | |||||
chrX:85059587
|
G | A | 1 | a0001c0001t0079g0235 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.394+3662G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059587 | ||||||
chrX:85059648
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.394+3723A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059648 | ||||||
chrX:85059839
|
T | C | 37 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(34): Show | 37 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.394+3914T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059839 | ||||||
chrX:85059925
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(239): Show | 245 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.394+4000T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059925 | ||||||
chrX:85059933
|
G | T | 1 | a0001c0001t0065g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.394+4008G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059933 | ||||||
chrX:85059974
|
T | A | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.394+4049T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85059974 | ||||||
chrX:85060061
|
G | A | 1 | a0001c0001t0007g0193 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.394+4136G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060061 | ||||||
chrX:85060062
|
T | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.394+4137T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060062 | ||||||
chrX:85060129
|
T | A | 16 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+4204T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060129 | ||||||
chrX:85060159
|
C | G | 16 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+4234C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060159 | ||||||
chrX:85060243
|
G | C | 1 | a0001c0001t0004g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.394+4318G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060243 | ||||||
chrX:85060248
|
G | T | 8 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0062g0016others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.394+4323G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060248 | ||||||
chrX:85060275
|
C | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.394+4350C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060275 | ||||||
chrX:85060354
|
G | A | 1 | a0001c0001t0020g0203 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.394+4429G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060354 | ||||||
chrX:85060446
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.394+4521T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060446 | ||||||
chrX:85060459
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.394+4534C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060459 | ||||||
chrX:85060532
|
G | A | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.394+4607G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060532 | ||||||
chrX:85060538
|
A | G | 29 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(26): Show | 29 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.394+4613A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060538 | ||||||
chrX:85060553
|
A | C | 3 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0116g0073 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394+4628A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060553 | ||||||
chrX:85060574
|
T | C | 3 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0116g0073 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394+4649T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060574 | ||||||
chrX:85060610
|
G | A | 3 | a0001c0001t0032g0008a0001c0001t0033g0009a0001c0001t0050g0014 | 3 | HG02109.hp1 HG02559.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.394+4685G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060610 | ||||||
chrX:85060632
|
T | A | 3 | a0001c0001t0026g0078a0001c0001t0026g0080a0001c0001t0075g0079 | 3 | HG01358.hp1 NA18954.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.394+4707T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060632 | ||||||
chrX:85060675
|
CTGTT | C | 1 | a0001c0001t0078g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.394+4754_394+4757d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85060675 | |||||
chrX:85060689
|
T | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.394+4764T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060689 | ||||||
chrX:85060805
|
A | G | 1 | a0001c0001t0003g0167 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.394+4880A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060805 | ||||||
chrX:85060866
|
C | T | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+4941C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060866 | ||||||
chrX:85060954
|
G | A | 1 | a0001c0001t0095g0067 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.394+5029G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060954 | ||||||
chrX:85060954
|
G | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.394+5029G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060954 | ||||||
chrX:85060959
|
A | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(186): Show | 191 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.394+5034A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85060959 | ||||||
chrX:85061086
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(73): Show | 77 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.394+5161A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061086 | ||||||
chrX:85061217
|
C | A | 2 | a0001c0001t0003g0165a0001c0001t0003g0196 | 2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.394+5292C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061217 | ||||||
chrX:85061434
|
C | T | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.394+5509C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061434 | ||||||
chrX:85061435
|
G | A | 1 | a0001c0001t0003g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.394+5510G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061435 | ||||||
chrX:85061468
|
C | T | 5 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+5543C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061468 | ||||||
chrX:85061538
|
G | A | 1 | a0001c0001t0002g0145 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.395-5589G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061538 | ||||||
chrX:85061590
|
T | G | 2 | a0001c0001t0004g0231a0001c0001t0038g0230 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.395-5537T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061590 | ||||||
chrX:85061644
|
C | T | 1 | a0001c0001t0005g0190 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.395-5483C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061644 | ||||||
chrX:85061775
|
C | G | 1 | a0001c0001t0062g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.395-5352C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061775 | ||||||
chrX:85061796
|
C | G | 9 | a0001c0001t0009g0124a0001c0001t0009g0128a0001c0001t0009g0169others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-5331C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061796 | ||||||
chrX:85061797
|
G | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-5330G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061797 | ||||||
chrX:85061837
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.395-5290C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061837 | ||||||
chrX:85061908
|
G | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 182 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.395-5219G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85061908 | ||||||
chrX:85062116
|
T | A | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-5011T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062116 | ||||||
chrX:85062118
|
T | TGCCTTCA others(13): Show |
4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-5008_395-4989d others(22): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85062118 | |||||
chrX:85062135
|
T | G | 5 | a0001c0001t0002g0145a0001c0001t0002g0149a0001c0001t0002g0154others(2): Show | 5 | HG00609.hp1 HG02027.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-4992T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062135 | ||||||
chrX:85062218
|
G | GT | 2 | a0001c0001t0065g0018a0001c0001t0066g0047 | 2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.395-4901dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85062218 | |||||
chrX:85062297
|
A | G | 1 | a0001c0001t0037g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.395-4830A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062297 | ||||||
chrX:85062315
|
C | G | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.395-4812C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062315 | ||||||
chrX:85062444
|
A | G | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4683A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062444 | ||||||
chrX:85062686
|
C | T | 1 | a0001c0001t0081g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.395-4441C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062686 | ||||||
chrX:85062727
|
GT | G | 3 | a0001c0001t0042g0222a0001c0001t0043g0221a0001c0001t0044g0218 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.395-4395delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85062727 | |||||
chrX:85062788
|
G | A | 7 | a0001c0001t0009g0124a0001c0001t0009g0128a0001c0001t0009g0169others(4): Show | 7 | HG02257.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.395-4339G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062788 | ||||||
chrX:85062853
|
G | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(180): Show | 185 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.395-4274G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062853 | ||||||
chrX:85062914
|
C | G | 1 | a0001c0001t0122g0063 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.395-4213C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062914 | ||||||
chrX:85062935
|
T | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.395-4192T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062935 | ||||||
chrX:85062955
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(187): Show | 192 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.395-4172A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85062955 | ||||||
chrX:85063074
|
G | A | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4053G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063074 | ||||||
chrX:85063120
|
C | A | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-4007C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063120 | ||||||
chrX:85063122
|
A | G | 1 | a0001c0001t0085g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.395-4005A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063122 | ||||||
chrX:85063144
|
T | A | 1 | a0001c0001t0003g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.395-3983T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063144 | ||||||
chrX:85063152
|
CT | C | 1 | a0001c0001t0011g0198 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.395-3974delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063152 | ||||||
chrX:85063352
|
A | AT | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-3767dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85063352 | |||||
chrX:85063541
|
G | A | 1 | a0001c0001t0025g0049 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.395-3586G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063541 | ||||||
chrX:85063577
|
A | T | 1 | a0001c0001t0073g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.395-3550A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063577 | ||||||
chrX:85063651
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.395-3476C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063651 | ||||||
chrX:85063652
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.395-3475G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063652 | ||||||
chrX:85063756
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.395-3371A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063756 | ||||||
chrX:85063775
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 114 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.395-3352T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063775 | ||||||
chrX:85063789
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.395-3338G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85063789 | ||||||
chrX:85063836
|
C | CT | 1 | a0001c0001t0027g0058 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.395-3284dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85063836 | |||||
chrX:85064081
|
A | G | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-3046A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064081 | ||||||
chrX:85064220
|
C | T | 8 | a0001c0001t0032g0008a0001c0001t0033g0009a0001c0001t0047g0011others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.395-2907C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064220 | ||||||
chrX:85064339
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.395-2788G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064339 | ||||||
chrX:85064340
|
A | AT | 30 | a0001c0001t0001g0140a0001c0001t0004g0224a0001c0001t0004g0226others(27): Show | 30 | HG00438.hp2 HG01081.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.395-2771dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064340 | |||||
chrX:85064340
|
A | ATT | 15 | a0001c0001t0006g0238a0001c0001t0006g0242a0001c0001t0006g0244others(12): Show | 15 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.395-2772_395-2771d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064340 | |||||
chrX:85064340
|
A | ATTT | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-2773_395-2771d others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064340 | |||||
chrX:85064340
|
AT | A | 1 | a0001c0001t0072g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.395-2771delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064340 | |||||
chrX:85064363
|
A | AT | 12 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0002g0145others(9): Show | 12 | HG00438.hp2 HG00609.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.395-2759dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064363 | |||||
chrX:85064530
|
T | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.395-2597T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064530 | ||||||
chrX:85064797
|
A | C | 9 | a0001c0001t0032g0008a0001c0001t0033g0009a0001c0001t0035g0219others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-2330A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85064797 | ||||||
chrX:85064852
|
G | GT | 1 | a0001c0001t0052g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.395-2267dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85064852 | |||||
chrX:85065058
|
G | T | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.395-2069G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065058 | ||||||
chrX:85065103
|
T | G | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-2024T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065103 | ||||||
chrX:85065128
|
T | C | 5 | a0001c0001t0002g0089a0001c0001t0002g0118a0001c0001t0005g0090others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-1999T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065128 | ||||||
chrX:85065205
|
G | GT | 1 | a0001c0001t0001g0206 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.395-1915dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85065205 | |||||
chrX:85065240
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.395-1887C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065240 | ||||||
chrX:85065546
|
C | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.395-1581C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065546 | ||||||
chrX:85065547
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.395-1580G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065547 | ||||||
chrX:85065553
|
G | A | 1 | a0001c0001t0004g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.395-1574G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065553 | ||||||
chrX:85065625
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(180): Show | 185 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.395-1502G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065625 | ||||||
chrX:85065934
|
G | A | 5 | a0001c0001t0010g0094a0001c0001t0010g0108a0001c0001t0012g0158others(2): Show | 5 | HG01255.hp1 HG02602.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-1193G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065934 | ||||||
chrX:85065976
|
C | T | 9 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0035g0219others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.395-1151C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85065976 | ||||||
chrX:85066040
|
G | A | 3 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0116g0073 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.395-1087G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066040 | ||||||
chrX:85066092
|
A | G | 5 | a0001c0001t0031g0003a0001c0001t0031g0061a0001c0001t0061g0071others(2): Show | 5 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-1035A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066092 | ||||||
chrX:85066249
|
G | A | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.395-878G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066249 | ||||||
chrX:85066386
|
C | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0117 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.395-741C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066386 | ||||||
chrX:85066541
|
A | G | 1 | a0001c0001t0052g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.395-586A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066541 | ||||||
chrX:85066595
|
C | T | 1 | a0001c0001t0099g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.395-532C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066595 | ||||||
chrX:85066636
|
T | TAA | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-490_395-489ins others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chrX | 85066636 | |||||
chrX:85066638
|
T | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-489T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066638 | ||||||
chrX:85066640
|
T | C | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.395-487T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066640 | ||||||
chrX:85066641
|
A | C | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-486A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066641 | ||||||
chrX:85066642
|
C | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-485C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85066642 | ||||||
chrX:85067061
|
G | A | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.395-66G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85067061 | ||||||
chrX:85067109
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.395-18T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 5/8 | chrX | 85067109 | ||||||
chrX:85067431
|
G | A | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.486+213G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067431 | ||||||
chrX:85067624
|
TA | T | 1 | a0001c0001t0104g0027 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.486+410delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067624 | |||||
chrX:85067625
|
A | AACACAC | 1 | a0001c0001t0017g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486+408_486+409ins others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067625 | |||||
chrX:85067627
|
A | AAAAC | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0003g0122 | 3 | NA19009.hp1 NA19012.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.486+410_486+411ins others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
A | AAC | 90 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0102others(87): Show | 90 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.486+448_486+449dup others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
A | AACAC | 20 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0091others(17): Show | 22 | HG00140.hp1 HG00558.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.486+446_486+449dup others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
A | AACACAC | 8 | a0001c0001t0002g0153a0001c0001t0004g0224a0001c0001t0009g0124others(5): Show | 8 | HG01169.hp2 HG02818.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+444_486+449dup others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
A | AACACACA others(1): Show |
15 | a0001c0001t0004g0226a0001c0001t0004g0228a0001c0001t0004g0231others(12): Show | 15 | HG01081.hp2 HG01109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.486+442_486+449dup others(8): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
A | AACACACA others(3): Show |
2 | a0001c0001t0004g0234a0001c0001t0011g0127 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.486+440_486+449dup others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
A | ACAC | 4 | a0001c0001t0001g0112a0001c0001t0001g0138a0001c0001t0001g0140others(1): Show | 4 | HG00438.hp2 HG02698.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+409_486+410ins others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067627 | ||||||
chrX:85067627
|
A | ACACAC | 1 | a0001c0001t0002g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.486+409_486+410ins others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067627 | ||||||
chrX:85067627
|
A | C | 1 | a0001c0001t0017g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486+409A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067627 | ||||||
chrX:85067627
|
AAC | A | 26 | a0001c0001t0001g0106a0001c0001t0002g0005a0001c0001t0002g0110others(23): Show | 26 | HG00642.hp1 HG00738.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.486+448_486+449del others(2): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
AACAC | A | 10 | a0001c0001t0016g0239a0001c0001t0016g0245a0001c0001t0030g0048others(7): Show | 10 | HG01346.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+446_486+449del others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
AACACACA others(3): Show |
A | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.486+440_486+449del others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067627
|
AACACACA others(11): Show |
A | 1 | a0001c0001t0003g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.486+432_486+449del others(18): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067627 | |||||
chrX:85067637
|
C | CACACACA others(31): Show |
1 | a0001c0001t0114g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.486+449_486+450ins others(38): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067637 | |||||
chrX:85067637
|
C | CACACACA others(29): Show |
3 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0115g0215 | 3 | HG02055.hp1 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.486+449_486+450ins others(36): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067637 | |||||
chrX:85067639
|
C | CACACACA others(17): Show |
1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486+444_486+445ins others(24): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067639 | |||||
chrX:85067738
|
C | A | 7 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0007g0162others(4): Show | 7 | NA18948.hp1 NA18954.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+520C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067738 | ||||||
chrX:85067807
|
AT | A | 1 | a0001c0001t0073g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.486+594delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067807 | |||||
chrX:85067873
|
TCTC | T | 1 | a0001c0001t0112g0019 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.486+659_486+661del others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067873 | |||||
chrX:85067902
|
TC | T | 1 | a0001c0001t0073g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.486+689delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85067902 | |||||
chrX:85067982
|
C | T | 1 | a0001c0001t0065g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.486+764C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85067982 | ||||||
chrX:85068032
|
A | AT | 1 | a0001c0001t0073g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.486+815dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85068032 | |||||
chrX:85068298
|
C | T | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.486+1080C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068298 | ||||||
chrX:85068334
|
G | A | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+1116G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068334 | ||||||
chrX:85068396
|
C | CT | 6 | a0001c0001t0003g0125a0001c0001t0005g0142a0001c0001t0034g0236others(3): Show | 6 | HG02027.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+1193dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85068396 | |||||
chrX:85068396
|
CT | C | 4 | a0001c0001t0021g0160a0001c0001t0035g0219a0001c0001t0058g0084others(1): Show | 4 | HG02897.hp2 HG03486.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+1193delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85068396 | |||||
chrX:85068412
|
C | CT | 3 | a0001c0001t0021g0159a0001c0001t0032g0008a0001c0001t0033g0009 | 3 | HG02109.hp1 HG02559.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.486+1205dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85068412 | |||||
chrX:85068412
|
CT | C | 1 | a0001c0001t0073g0053 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.486+1205delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85068412 | |||||
chrX:85068465
|
G | GC | 1 | a0001c0001t0027g0058 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.486+1250dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85068465 | |||||
chrX:85068625
|
C | T | 1 | a0001c0001t0034g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.486+1407C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068625 | ||||||
chrX:85068632
|
CT | C | 8 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0062g0016others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.486+1415delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068632 | ||||||
chrX:85068653
|
G | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486+1435G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068653 | ||||||
chrX:85068829
|
T | A | 9 | a0001c0001t0008g0085a0001c0001t0008g0086a0001c0001t0008g0101others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+1611T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068829 | ||||||
chrX:85068904
|
T | C | 2 | a0001c0001t0002g0115a0001c0001t0002g0117 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.486+1686T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85068904 | ||||||
chrX:85069183
|
AT | A | 1 | a0001c0001t0001g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.486+1974delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069183 | |||||
chrX:85069348
|
TA | T | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2135delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069348 | |||||
chrX:85069417
|
A | G | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.486+2199A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85069417 | ||||||
chrX:85069522
|
A | C | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2304A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85069522 | ||||||
chrX:85069545
|
G | GA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2328dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069545 | |||||
chrX:85069610
|
T | TA | 48 | a0001c0001t0001g0139a0001c0001t0001g0176a0001c0001t0001g0186others(45): Show | 49 | HG00621.hp1 HG00733.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.486+2419dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069610 | |||||
chrX:85069610
|
T | TAA | 9 | a0001c0001t0004g0229a0001c0001t0006g0238a0001c0001t0012g0158others(6): Show | 9 | HG01169.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+2418_486+2419d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069610 | |||||
chrX:85069610
|
T | TAAA | 1 | a0001c0001t0018g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.486+2417_486+2419d others(5): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069610 | |||||
chrX:85069610
|
TA | T | 15 | a0001c0001t0001g0147a0001c0001t0030g0048a0001c0001t0030g0072others(12): Show | 15 | HG01256.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.486+2419delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069610 | |||||
chrX:85069771
|
TA | T | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2557delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069771 | |||||
chrX:85069778
|
G | GA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2562dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069778 | |||||
chrX:85069789
|
T | TA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2576dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069789 | |||||
chrX:85069812
|
T | C | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+2594T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85069812 | ||||||
chrX:85069895
|
GC | G | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2679delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069895 | |||||
chrX:85069928
|
A | AC | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2711dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85069928 | |||||
chrX:85069929
|
C | T | 1 | a0001c0001t0020g0185 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.486+2711C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85069929 | ||||||
chrX:85070177
|
A | T | 2 | a0001c0001t0026g0078a0001c0001t0026g0080 | 2 | NA18954.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.486+2959A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070177 | ||||||
chrX:85070184
|
TA | T | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+2970delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070184 | |||||
chrX:85070232
|
A | AG | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+3016dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070232 | |||||
chrX:85070240
|
G | GC | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+3024dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070240 | |||||
chrX:85070287
|
GT | G | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+3072delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070287 | |||||
chrX:85070361
|
T | C | 1 | a0001c0001t0107g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.486+3143T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070361 | ||||||
chrX:85070395
|
T | TA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+3179dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070395 | |||||
chrX:85070405
|
C | CA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+3188dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070405 | |||||
chrX:85070411
|
AT | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486+3198delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070411 | |||||
chrX:85070413
|
T | TA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+3195_486+3196i others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070413 | ||||||
chrX:85070466
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(157): Show | 162 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.486+3248G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070466 | ||||||
chrX:85070501
|
T | TA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+3285dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070501 | |||||
chrX:85070504
|
C | T | 3 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024 | 3 | HG01891.hp2 HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.486+3286C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070504 | ||||||
chrX:85070559
|
T | A | 3 | a0001c0001t0032g0008a0001c0001t0033g0009a0001c0001t0050g0014 | 3 | HG02109.hp1 HG02559.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.486+3341T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070559 | ||||||
chrX:85070582
|
TA | T | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.486+3367delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070582 | |||||
chrX:85070615
|
A | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.487-3383A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070615 | ||||||
chrX:85070646
|
A | AT | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.487-3350dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070646 | |||||
chrX:85070685
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.487-3313C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070685 | ||||||
chrX:85070810
|
G | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.487-3188G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070810 | ||||||
chrX:85070814
|
A | AT | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.487-3183dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070814 | |||||
chrX:85070819
|
C | CA | 14 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0211others(11): Show | 14 | HG01255.hp1 HG02738.hp1 HG04204.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-3165dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85070819 | |||||
chrX:85070820
|
A | C | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.487-3178A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85070820 | ||||||
chrX:85071121
|
A | G | 1 | a0001c0001t0025g0049 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.487-2877A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071121 | ||||||
chrX:85071135
|
T | TG | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.487-2860dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85071135 | |||||
chrX:85071138
|
G | A | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.487-2860G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071138 | ||||||
chrX:85071223
|
A | G | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-2775A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071223 | ||||||
chrX:85071353
|
T | C | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.487-2645T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071353 | ||||||
chrX:85071416
|
G | A | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.487-2582G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071416 | ||||||
chrX:85071441
|
A | AT | 1 | a0001c0001t0107g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.487-2547dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85071441 | |||||
chrX:85071620
|
C | A | 34 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(31): Show | 34 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.487-2378C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071620 | ||||||
chrX:85071666
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.487-2332T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85071666 | ||||||
chrX:85072581
|
C | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(72): Show | 76 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.487-1417C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072581 | ||||||
chrX:85072615
|
G | A | 1 | a0001c0001t0070g0081 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.487-1383G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072615 | ||||||
chrX:85072717
|
A | G | 22 | a0001c0001t0027g0035a0001c0001t0027g0058a0001c0001t0028g0042others(19): Show | 22 | HG00621.hp1 HG02004.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.487-1281A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072717 | ||||||
chrX:85072768
|
TA | T | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.487-1223delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85072768 | |||||
chrX:85072895
|
A | C | 8 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0007g0162others(5): Show | 8 | HG02040.hp1 NA18948.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-1103A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072895 | ||||||
chrX:85072935
|
G | A | 9 | a0001c0001t0015g0007a0001c0001t0030g0048a0001c0001t0030g0072others(6): Show | 10 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.487-1063G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072935 | ||||||
chrX:85072945
|
C | T | 1 | a0001c0001t0075g0079 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.487-1053C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072945 | ||||||
chrX:85072965
|
T | C | 5 | a0001c0001t0062g0016a0001c0001t0063g0051a0001c0001t0064g0024others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1033T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85072965 | ||||||
chrX:85073208
|
TA | T | 1 | a0001c0001t0006g0244 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.487-784delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85073208 | |||||
chrX:85073247
|
T | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(170): Show | 174 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.487-751T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073247 | ||||||
chrX:85073377
|
A | T | 3 | a0001c0001t0042g0222a0001c0001t0043g0221a0001c0001t0044g0218 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.487-621A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073377 | ||||||
chrX:85073674
|
C | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG01257.hp2 HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.487-324C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073674 | ||||||
chrX:85073743
|
TAAAA | T | 2 | a0001c0001t0001g0133a0001c0001t0002g0131 | 2 | NA18963.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.487-251_487-248del others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85073743 | |||||
chrX:85073744
|
A | T | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.487-254A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073744 | ||||||
chrX:85073757
|
T | C | 27 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0123others(24): Show | 27 | HG01934.hp1 HG02165.hp2 HG03942.hp1 others(24): Show |
intron_variant | MODIFIER | c.487-241T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | chrX | 85073757 | ||||||
chrX:85073827
|
A | AT | 1 | a0001c0001t0001g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.487-166dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chrX | 85073827 | |||||
chrX:85074197
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.601-77G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 7/8 | chrX | 85074197 | ||||||
chrX:85074558
|
A | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718+167A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85074558 | ||||||
chrX:85074664
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.718+273A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85074664 | ||||||
chrX:85074966
|
C | CA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+578dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85074966 | |||||
chrX:85075063
|
TA | T | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+673delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075063 | ||||||
chrX:85075099
|
A | G | 1 | a0001c0001t0037g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.718+708A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075099 | ||||||
chrX:85075114
|
C | A | 1 | a0001c0001t0008g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.718+723C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075114 | ||||||
chrX:85075116
|
C | T | 1 | a0001c0001t0011g0127 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.718+725C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075116 | ||||||
chrX:85075150
|
AT | A | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+761delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85075150 | |||||
chrX:85075159
|
T | C | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718+768T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075159 | ||||||
chrX:85075169
|
A | T | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+778A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075169 | ||||||
chrX:85075238
|
G | GA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+847_718+848ins others(1): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075238 | ||||||
chrX:85075335
|
G | GC | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+948dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85075335 | |||||
chrX:85075487
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.718+1096T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075487 | ||||||
chrX:85075502
|
A | AT | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1113dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85075502 | |||||
chrX:85075516
|
A | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(170): Show | 174 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.718+1125A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075516 | ||||||
chrX:85075537
|
T | TC | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1148dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85075537 | |||||
chrX:85075548
|
C | CT | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1158dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85075548 | |||||
chrX:85075578
|
GT | G | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1192delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85075578 | |||||
chrX:85075625
|
T | A | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1234T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075625 | ||||||
chrX:85075652
|
C | A | 1 | a0001c0001t0106g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.718+1261C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075652 | ||||||
chrX:85075903
|
A | G | 1 | a0001c0001t0108g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718+1512A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075903 | ||||||
chrX:85075914
|
G | GT | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1523_718+1524i others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85075914 | ||||||
chrX:85075983
|
A | AT | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1593dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85075983 | |||||
chrX:85076014
|
G | T | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.718+1623G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076014 | ||||||
chrX:85076104
|
T | TC | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1716dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076104 | |||||
chrX:85076219
|
TG | T | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1834delG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076219 | |||||
chrX:85076236
|
G | T | 2 | a0001c0001t0080g0070a0001c0001t0082g0069 | 2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.718+1845G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076236 | ||||||
chrX:85076263
|
G | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+1872G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076263 | ||||||
chrX:85076299
|
C | CT | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+1908_718+1909i others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076299 | ||||||
chrX:85076324
|
A | AT | 2 | a0001c0001t0015g0007a0001c0001t0047g0011 | 3 | HG02818.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.718+1946dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076324 | |||||
chrX:85076473
|
A | AG | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2082_718+2083i others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076473 | ||||||
chrX:85076536
|
A | AG | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2146dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076536 | |||||
chrX:85076551
|
G | GC | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2162dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076551 | |||||
chrX:85076552
|
C | T | 2 | a0001c0001t0009g0128a0001c0001t0011g0127 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.718+2161C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076552 | ||||||
chrX:85076660
|
TA | T | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2272delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076660 | |||||
chrX:85076903
|
A | T | 5 | a0001c0001t0018g0168a0001c0001t0018g0197a0001c0001t0019g0208others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+2512A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85076903 | ||||||
chrX:85076930
|
T | TG | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2540dupG | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076930 | |||||
chrX:85076942
|
GC | G | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2553delC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076942 | |||||
chrX:85076965
|
G | GT | 182 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(179): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.718+2583dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076965 | |||||
chrX:85076995
|
T | TTA | 15 | a0001c0001t0001g0172a0001c0001t0001g0186a0001c0001t0001g0187others(12): Show | 15 | HG00558.hp2 HG00733.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.718+2625_718+2626d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATA | 4 | a0001c0001t0024g0004a0001c0001t0067g0083a0001c0001t0068g0082others(1): Show | 5 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+2623_718+2626d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(1): Show |
1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718+2619_718+2626d others(10): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(7): Show |
10 | a0001c0001t0006g0238a0001c0001t0006g0244a0001c0001t0006g0246others(7): Show | 10 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.718+2613_718+2626d others(16): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(11): Show |
3 | a0001c0001t0006g0242a0001c0001t0006g0247a0001c0001t0037g0223 | 3 | HG01884.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.718+2609_718+2626d others(20): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(15): Show |
5 | a0001c0001t0004g0232a0001c0001t0036g0225a0001c0001t0038g0230others(2): Show | 5 | HG01081.hp2 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+2605_718+2626d others(24): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(17): Show |
3 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227 | 3 | HG01109.hp1 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.718+2626_718+2627i others(26): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(19): Show |
4 | a0001c0001t0004g0229a0001c0001t0004g0231a0001c0001t0004g0233others(1): Show | 4 | HG02280.hp1 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+2626_718+2627i others(28): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(21): Show |
1 | a0001c0001t0004g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.718+2626_718+2627i others(30): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0114g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718+2626_718+2627i others(36): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(55): Show |
1 | a0001c0001t0042g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.718+2626_718+2627i others(64): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
T | TTATATAT others(61): Show |
2 | a0001c0001t0043g0221a0001c0001t0044g0218 | 2 | NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.718+2626_718+2627i others(70): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
TTA | T | 31 | a0001c0001t0008g0085a0001c0001t0008g0086a0001c0001t0008g0101others(28): Show | 31 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.718+2625_718+2626d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85076995
|
TTATA | T | 2 | a0001c0001t0015g0007a0001c0001t0108g0214 | 3 | HG02970.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.718+2623_718+2626d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85076995 | |||||
chrX:85077016
|
T | C | 9 | a0001c0001t0001g0102a0001c0001t0030g0048a0001c0001t0030g0072others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.718+2625T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077016 | ||||||
chrX:85077016
|
T | TATATATA others(15): Show |
1 | a0001c0001t0039g0220 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.718+2626_718+2627i others(24): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077016 | |||||
chrX:85077033
|
G | GTA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2651_718+2652d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077033 | |||||
chrX:85077044
|
C | T | 3 | a0001c0001t0042g0222a0001c0001t0043g0221a0001c0001t0044g0218 | 3 | NA18952.hp1 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.718+2653C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077044 | ||||||
chrX:85077059
|
ACG | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718+2669_718+2670d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077059 | ||||||
chrX:85077061
|
G | GTA | 4 | a0001c0001t0109g0020a0001c0001t0110g0025a0001c0001t0111g0052others(1): Show | 4 | HG02647.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+2683_718+2684d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077061 | |||||
chrX:85077061
|
GTA | G | 35 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(32): Show | 35 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.718+2683_718+2684d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077061 | |||||
chrX:85077063
|
A | G | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718+2672A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077063 | ||||||
chrX:85077069
|
A | AG | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2678_718+2679i others(3): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077069 | ||||||
chrX:85077072
|
TATAC | T | 2 | a0001c0001t0006g0242a0001c0001t0006g0247 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.718+2685_718+2688d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077072 | |||||
chrX:85077074
|
T | C | 4 | a0001c0001t0015g0007a0001c0001t0030g0048a0001c0001t0030g0072others(1): Show | 5 | HG02622.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+2683T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077074 | ||||||
chrX:85077076
|
C | CAT | 1 | a0001c0001t0106g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.718+2701_718+2702d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077076 | |||||
chrX:85077076
|
CAT | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(131): Show | 135 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.718+2701_718+2702d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077076 | |||||
chrX:85077078
|
T | C | 7 | a0001c0001t0006g0242a0001c0001t0006g0247a0001c0001t0062g0016others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.718+2687T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077078 | ||||||
chrX:85077092
|
T | C | 1 | a0001c0001t0077g0021 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.718+2701T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077092 | ||||||
chrX:85077092
|
T | TAC | 4 | a0001c0001t0109g0020a0001c0001t0110g0025a0001c0001t0111g0052others(1): Show | 4 | HG02647.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+2709_718+2710d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077092 | |||||
chrX:85077102
|
T | C | 2 | a0001c0001t0025g0046a0001c0001t0111g0052 | 2 | HG01074.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.718+2711T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077102 | ||||||
chrX:85077111
|
AT | A | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2727delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077111 | |||||
chrX:85077113
|
T | A | 2 | a0001c0001t0020g0185a0001c0001t0020g0203 | 2 | HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.718+2722T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077113 | ||||||
chrX:85077141
|
T | TA | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+2751dupA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077141 | |||||
chrX:85077245
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.718+2854T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077245 | ||||||
chrX:85077264
|
C | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+2873C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077264 | ||||||
chrX:85077271
|
C | T | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+2880C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077271 | ||||||
chrX:85077353
|
C | T | 1 | a0001c0001t0094g0032 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.718+2962C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077353 | ||||||
chrX:85077743
|
AT | A | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+3355delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077743 | |||||
chrX:85077781
|
C | CT | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+3395dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85077781 | |||||
chrX:85077851
|
G | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.718+3460G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077851 | ||||||
chrX:85077871
|
GTT | G | 1 | a0001c0001t0096g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.718+3481_718+3482d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85077871 | ||||||
chrX:85078060
|
G | C | 1 | a0001c0001t0052g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.718+3669G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078060 | ||||||
chrX:85078075
|
A | C | 2 | a0001c0001t0003g0093a0001c0001t0035g0219 | 2 | HG03486.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.718+3684A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078075 | ||||||
chrX:85078241
|
T | A | 3 | a0001c0001t0119g0033a0001c0001t0120g0041a0001c0001t0122g0063 | 3 | NA18955.hp1 NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.718+3850T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078241 | ||||||
chrX:85078296
|
C | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+3905C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078296 | ||||||
chrX:85078424
|
T | G | 2 | a0001c0001t0009g0124a0001c0001t0009g0169 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.718+4033T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078424 | ||||||
chrX:85078425
|
G | C | 2 | a0001c0001t0009g0124a0001c0001t0009g0169 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.718+4034G>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078425 | ||||||
chrX:85078443
|
G | A | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718+4052G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078443 | ||||||
chrX:85078449
|
C | A | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718+4058C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078449 | ||||||
chrX:85078498
|
T | C | 4 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0232others(1): Show | 4 | HG01081.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+4107T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078498 | ||||||
chrX:85078730
|
C | A | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+4339C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078730 | ||||||
chrX:85078746
|
T | A | 3 | a0001c0001t0008g0202a0001c0001t0014g0173a0001c0001t0014g0201 | 3 | HG01243.hp1 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.718+4355T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078746 | ||||||
chrX:85078859
|
A | C | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+4468A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078859 | ||||||
chrX:85078867
|
T | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.718+4476T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078867 | ||||||
chrX:85078881
|
GCTCT | G | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.718+4493_718+4496d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85078881 | |||||
chrX:85078999
|
A | T | 1 | a0001c0001t0018g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.718+4608A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85078999 | ||||||
chrX:85079031
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.718+4640T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079031 | ||||||
chrX:85079230
|
T | A | 1 | a0001c0001t0038g0230 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.718+4839T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079230 | ||||||
chrX:85079485
|
G | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.718+5094G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079485 | ||||||
chrX:85079519
|
G | A | 6 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0138others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.718+5128G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079519 | ||||||
chrX:85079551
|
C | CT | 5 | a0001c0001t0106g0015a0001c0001t0109g0020a0001c0001t0110g0025others(2): Show | 5 | HG02647.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+5167dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85079551 | |||||
chrX:85079626
|
C | T | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+5235C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079626 | ||||||
chrX:85079845
|
C | G | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.718+5454C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079845 | ||||||
chrX:85079876
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.718+5485G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079876 | ||||||
chrX:85079949
|
T | G | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718+5558T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85079949 | ||||||
chrX:85080285
|
G | A | 3 | a0001c0001t0030g0048a0001c0001t0030g0072a0001c0001t0116g0073 | 3 | HG02622.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.718+5894G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080285 | ||||||
chrX:85080349
|
C | T | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.718+5958C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080349 | ||||||
chrX:85080497
|
T | A | 1 | a0001c0001t0008g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.718+6106T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080497 | ||||||
chrX:85080581
|
G | A | 1 | a0001c0001t0085g0037 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.718+6190G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080581 | ||||||
chrX:85080676
|
A | C | 4 | a0001c0001t0004g0228a0001c0001t0004g0229a0001c0001t0004g0232others(1): Show | 4 | HG01081.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.718+6285A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080676 | ||||||
chrX:85080963
|
C | G | 1 | a0001c0001t0049g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.718+6572C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85080963 | ||||||
chrX:85080976
|
CTA | C | 3 | a0001c0001t0010g0006a0001c0001t0010g0192a0001c0001t0051g0006 | 3 | HG02922.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.718+6587_718+6588d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85080976 | |||||
chrX:85081065
|
T | C | 1 | a0001c0001t0081g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.719-6525T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081065 | ||||||
chrX:85081108
|
G | T | 2 | a0001c0001t0074g0065a0001c0001t0086g0034 | 2 | NA18963.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.719-6482G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081108 | ||||||
chrX:85081228
|
G | A | 3 | a0001c0001t0019g0208a0001c0001t0019g0210a0001c0001t0055g0209 | 3 | HG01891.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.719-6362G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081228 | ||||||
chrX:85081229
|
G | A | 5 | a0001c0001t0018g0168a0001c0001t0018g0197a0001c0001t0019g0208others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.719-6361G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081229 | ||||||
chrX:85081382
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(179): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.719-6208G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081382 | ||||||
chrX:85081413
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.719-6177G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081413 | ||||||
chrX:85081612
|
T | C | 9 | a0001c0001t0008g0085a0001c0001t0008g0086a0001c0001t0008g0101others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.719-5978T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081612 | ||||||
chrX:85081666
|
T | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.719-5924T>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081666 | ||||||
chrX:85081677
|
A | T | 1 | a0001c0001t0105g0217 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.719-5913A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081677 | ||||||
chrX:85081705
|
C | T | 28 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(25): Show | 28 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.719-5885C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081705 | ||||||
chrX:85081734
|
C | T | 1 | a0001c0001t0081g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.719-5856C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081734 | ||||||
chrX:85081852
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(179): Show | 184 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.719-5738G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081852 | ||||||
chrX:85081879
|
C | G | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-5711C>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081879 | ||||||
chrX:85081963
|
C | T | 1 | a0001c0001t0036g0225 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.719-5627C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85081963 | ||||||
chrX:85082063
|
A | G | 1 | a0001c0001t0079g0235 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.719-5527A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082063 | ||||||
chrX:85082340
|
A | G | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.719-5250A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082340 | ||||||
chrX:85082395
|
C | T | 1 | a0001c0001t0044g0218 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.719-5195C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082395 | ||||||
chrX:85082566
|
GA | G | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-5016delA | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85082566 | |||||
chrX:85082608
|
G | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(176): Show | 181 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.719-4982G>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082608 | ||||||
chrX:85082707
|
A | G | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-4883A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082707 | ||||||
chrX:85082713
|
G | A | 1 | a0001c0001t0047g0011 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.719-4877G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082713 | ||||||
chrX:85082806
|
A | C | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-4784A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082806 | ||||||
chrX:85082921
|
C | T | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-4669C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85082921 | ||||||
chrX:85083601
|
T | C | 1 | a0001c0001t0027g0035 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.719-3989T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85083601 | ||||||
chrX:85083601
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.719-3989T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85083601 | ||||||
chrX:85083741
|
T | G | 1 | a0001c0001t0050g0014 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.719-3849T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85083741 | ||||||
chrX:85083946
|
C | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.719-3644C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85083946 | ||||||
chrX:85084109
|
T | C | 1 | a0001c0001t0060g0022 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.719-3481T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084109 | ||||||
chrX:85084134
|
C | CT | 16 | a0001c0001t0001g0104a0001c0001t0001g0186a0001c0001t0003g0130others(13): Show | 17 | HG00438.hp1 HG00673.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.719-3437dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85084134 | |||||
chrX:85084134
|
CT | C | 6 | a0001c0001t0001g0147a0001c0001t0032g0008a0001c0001t0033g0009others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.719-3437delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85084134 | |||||
chrX:85084134
|
CTT | C | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.719-3438_719-3437d others(4): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85084134 | |||||
chrX:85084198
|
C | T | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.719-3392C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084198 | ||||||
chrX:85084380
|
C | T | 2 | a0001c0001t0076g0031a0001c0001t0091g0059 | 2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.719-3210C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084380 | ||||||
chrX:85084404
|
G | A | 4 | a0001c0001t0109g0020a0001c0001t0110g0025a0001c0001t0111g0052others(1): Show | 4 | HG02647.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.719-3186G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084404 | ||||||
chrX:85084522
|
G | GT | 4 | a0001c0001t0025g0049a0001c0001t0032g0008a0001c0001t0033g0009others(1): Show | 4 | HG01175.hp2 HG02109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-3057dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85084522 | |||||
chrX:85084522
|
GT | G | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-3057delT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85084522 | |||||
chrX:85084778
|
T | G | 1 | a0001c0001t0034g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.719-2812T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084778 | ||||||
chrX:85084789
|
T | G | 1 | a0001c0001t0034g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.719-2801T>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85084789 | ||||||
chrX:85085087
|
A | G | 1 | a0001c0001t0034g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.719-2503A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85085087 | ||||||
chrX:85085238
|
CAAAG | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.719-2348_719-2345d others(6): Show |
APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85085238 | |||||
chrX:85085398
|
C | T | 1 | a0001c0001t0062g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.719-2192C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85085398 | ||||||
chrX:85085399
|
G | A | 1 | a0001c0001t0035g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.719-2191G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85085399 | ||||||
chrX:85086042
|
A | T | 2 | a0001c0001t0006g0242a0001c0001t0006g0247 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.719-1548A>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086042 | ||||||
chrX:85086145
|
A | C | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.719-1445A>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086145 | ||||||
chrX:85086192
|
T | C | 2 | a0001c0001t0032g0008a0001c0001t0033g0009 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.719-1398T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086192 | ||||||
chrX:85086235
|
C | T | 1 | a0001c0001t0103g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.719-1355C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086235 | ||||||
chrX:85086704
|
A | AT | 8 | a0001c0001t0007g0207a0001c0001t0037g0223a0001c0001t0059g0194others(5): Show | 8 | HG00621.hp1 HG01884.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.719-873dupT | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85086704 | |||||
chrX:85086722
|
C | T | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-868C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086722 | ||||||
chrX:85086763
|
G | A | 1 | a0001c0001t0008g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.719-827G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086763 | ||||||
chrX:85086788
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 179 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.719-802T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086788 | ||||||
chrX:85086793
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 179 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.719-797G>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086793 | ||||||
chrX:85086800
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(174): Show | 179 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.719-790C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086800 | ||||||
chrX:85086910
|
A | G | 4 | a0001c0001t0105g0217a0001c0001t0108g0214a0001c0001t0114g0216others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-680A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086910 | ||||||
chrX:85086939
|
T | C | 2 | a0001c0001t0009g0124a0001c0001t0009g0169 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.719-651T>C | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086939 | ||||||
chrX:85086941
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.719-649C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086941 | ||||||
chrX:85086967
|
A | G | 1 | a0001c0001t0015g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.719-623A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85086967 | ||||||
chrX:85086991
|
G | GC | 1 | a0001c0001t0001g0104 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.719-596dupC | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chrX | 85086991 | |||||
chrX:85087016
|
A | G | 33 | a0001c0001t0004g0224a0001c0001t0004g0226a0001c0001t0004g0227others(30): Show | 33 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.719-574A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087016 | ||||||
chrX:85087022
|
C | A | 1 | a0001c0001t0025g0046 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.719-568C>A | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087022 | ||||||
chrX:85087213
|
A | G | 1 | a0001c0001t0046g0040 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.719-377A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087213 | ||||||
chrX:85087234
|
C | T | 4 | a0001c0001t0015g0007a0001c0001t0030g0048a0001c0001t0030g0072others(1): Show | 5 | HG02622.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.719-356C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087234 | ||||||
chrX:85087297
|
C | T | 1 | a0001c0001t0099g0036 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.719-293C>T | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087297 | ||||||
chrX:85087321
|
A | G | 1 | a0001c0001t0005g0184 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.719-269A>G | APOOL | ENSG00000155008.16 | transcript | ENST00000373173.7 | protein_coding | 8/8 | chrX | 85087321 |